Skip to main content
NCBI home page
Scientific Reports logoLink to Scientific Reports
. 2016 Sep 16;6:33434. doi: 10.1038/srep33434

Discovery and Optimization of N-Substituted 2-(4-pyridinyl)thiazole carboxamides against Tumor Growth through Regulating Angiogenesis Signaling Pathways

Wenbo Zhou 1,*, Wenshu Tang 1,*, Zhenliang Sun 2,*, Yunqi Li 1, Yanmin Dong 1, Haixiang Pei 1, Yangrui Peng 1, Jinhua Wang 1, Ting Shao 1, Zhenran Jiang 3, Zhengfang Yi 1,a, Yihua Chen 1,b
PMCID: PMC5025770  PMID: 27633259

Abstract

Inhibition of angiogenesis is considered as one of the desirable pathways for the treatment of tumor growth and metastasis. Herein we demonstrated that a series of pyridinyl-thiazolyl carboxamide derivatives were designed, synthesized and examined against angiogenesis through a colony formation and migration assays of human umbilical vein endothelial cells (HUVECs) in vitro. A structure-activity relationship (SAR) study was carried out and optimization toward this series of compounds resulted in the discovery of N-(3-methoxyphenyl)-4-methyl-2-(2-propyl-4-pyridinyl)thiazole-5-carboxamide (3k). The results indicated that compound 3k showed similar or better effects compared to Vandetanib in suppressing HUVECs colony formation and migration as well as VEGF-induced angiogenesis in the aortic ring spreading model and chick embryo chorioallantoic membrane (CAM) model. More importantly, compound 3k also strongly blocked tumor growth with the dosage of 30 mg/kg/day, and subsequent mechanism exploration suggested that this series of compounds took effect mainly through angiogenesis signaling pathways. Together, these results suggested compound 3k may serve as a lead for a novel class of angiogenesis inhibitors for cancer treatments.

Angiogenesis is generally applied to the formation of new blood vessels from pre-existing vessels network through a combination of sprouting, proliferation, and remodeling processes1. Physiological angiogenesis is essential in the process of tissues reproduction, development and wound repair2, while pathological angiogenesis is necessary for progression of tumor growth and metastasis beyond a microscopic size3. The induction of tumor vasculature is believed to be one of the key steps for the sustained growth of tumors2, and tumor neo-angiogenesis also provides the principal route of tumor metastasis which is largely dependent on new vessels4. Inhibition of angiogenesis is considered as one of the desirable pathways for cancer treatments primarily due to the potential low toxicity or resistance5, as well as suitable for a broad spectrum of tumor types6. The proposed clinical benefit of cancer therapeutics via inhibiting angiogenesis has been widely reviewed7. For example, less drug resistance may be induced when untransformed endothelial cells rather than genetically unstable cancer cells were targeted8. More importantly, the therapeutics also may be still effective after drug resistance has already occurred5. In addition, slowly growing tumors are usually refractory if treated with standard cytotoxic cancer therapy, but which are responsive to continuous, low-dose anti-angiogenic drugs9. Furthermore, abnormal expression of the targets derived from tumor-related genes are not necessary required because anti-angiogenic drugs primarily target the vasculature rather than the tumor itself8. With respect to validation of the anti-angiogenesis concept, the most notable drug is the vascular endothelial growth factor (VEGF) monoclonal antibody, Bevacizumab (Avastin®, Genentech Ltd), which was approved as the first anti-angiogenic drug by the FDA in 2004 for the treatment of cancer10. In addition, compound 1 (Caprelsa®, Vandetanib, Fig. 1) was approved as one of VEGFR2 inhibitors by the FDA for the treatment of medullary thyroid carcinoma through inhibiting angiogenesis in 2011. Many research groups have consequently carried out substantial efforts in order to explore non-peptide small molecular inhibitors of angiogenesis, which have led to the identification of several classes of inhibitors5,11,12,13,14,15.

Figure 1.

Figure 1

Open in a new tab

Structures of vandetanib (1) and several representative anticancer agents containing arylthiazole scaffold (2a–e).

Arylthiazole scaffold is a well known privileged structure against various diseases, especially in the antitumor field, which was mentioned for various biological targets16,17,18,19. For example, 7-mercapto-N-(4-phenyl-2-thiazolyl)heptanamide (2a) was reported as novel HDAC inhibitors20, (2-phenyl-4-thiazolyl)-(3,4,5-trimethoxyphenyl)-methanone (2b) exerted its anti-cancer activities through inhibiting tubulin polymerization17, phenyl-(5-(4-pyridinyl)-2-thiazolyl)-amine (2c) took effect via inducing autophagic cell death21, N-(4-(2,4-dimethylphenyl) -2-thiazolyl)benzamide (2d) was regarded as a Nek2/Hec1 inhibitor22, Fatostatin (2e) was designed and optimized against metabolic diseases as well as cancer progression through blocking activation of sterol regulatory element-binding proteins (SREBP) (Fig. 1)23. However, the effects of pyridinyl-thiazolyl carboxamide derivatives against tumor angiogenesis have not been thoroughly explored to date. Our goal is focused on the design and development of novel small molecular inhibitors for the treatment of cancer growth and metastasis through inhibiting angiogenesis in view of tumor metastasis responsible for above 90% solid tumor cancer death24,25. With the inspiration of above research success against cancer, a series of pyridinyl-thiazolyl carboxamide derivatives were designed and synthesized through analysis of their key scaffolds based on the expectation of inhibition of angiogenesis (Fig. 2).

Figure 2. Design strategy of novel potential anti-angiogenic compounds based on arylthiazole scaffold.

Figure 2

Open in a new tab

In this study, the effects of the series of pyridinyl-thiazolyl carboxamide derivatives were firstly examined against angiogenesis through a colony formation assay of human umbilical vein endothelial cells (HUVECs) in vitro. A structure-activity relationship (SAR) study was carried out and indicated that compounds 3k-s and 4b showed good inhibitions against HUVECs colony formation comparable to the approved drug 1, subsequently they were explored against HUVECs migration and found 3k showed the best anti-migration effect among the investigated ones and almost one-fold better than the positive control 1. Compound 3k was consequently chosen to evaluate the effects of neovascularization in the CAM assay and microvessel formation in the rat aortic ring ex vivo. More importantly, compound 3k was also further explored the efficacy against tumor growth in vivo. The results demonstrated that compound 3k not only suppressed tumor growth and angiogenesis but also blocked tumor cell migration, and subsequent mechanism exploration suggested that this series of compounds took effect mainly through angiogenesis signaling pathways, such as FAK-Src-Paxillin, JNK-c-Jun and ERK1/2-c-Jun, etc. All of the results indicate that these compounds are attractive as potential candidates for the treatment of tumor growth and metastasis in future.

Material and Methods

Biology

Cell culture and colony formation assay

HUVECs (Sciencell Research Laboratories, San Diego, CA, USA) were purchased from Science Research Laboratories and cultured in complete ECM (Sciencell) supplemented with 5% FBS. Bcap37 cells were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA) and maintained in DMEM supplemented with 10% FBS (Gibco BRL Life Technologies, Eggenstein, Germany). All cells were maintained at log phase at 37 °C with 5% carbon dioxide. Colony formation assay was performed as described previously26. Briefly, suspensions of HUVECs were seeded at a density of 2 × 103 in 12-well plates, and treated with indicated concentrations of compounds. After incubation at 37 °C with 5% of CO2 for 7 days until the visible clones appeared, cells were fixed with methanol for 15 min, then the cells were stained with crystal violet solution for 15 min before washing with PBS and air-drying. All the experiments were repeated 3 times and the average values were reported.

In vitro wound healing and transwell migration assay

Wound healing and transwell migration assay was performed as described previously27. For wound healing assay, 1 × 104 HUVECs were seeded with gelatin on a six-well plate. Upon reaching about 90% confluence, the cell monolayer was scraped by a sterile 0.1 mL pipette tip to create wounds, and HUVECs were seeded with or without different concentrations of compounds (0.5, 2, 10 and 20 μM). After 12 h incubation at 37 °C, 5% CO2, cells were fixed and photographed. The migrated cells were manually quantified. The percentage inhibition of migration was expressed using 100% as the number of migratory cells in the untreated control group. For transwell assay, 1 × 104 HUVECs were seeded in the upper chamber of transwell with serum-free medium and 500 μL of medium (containing 10% FBS) was added in the bottom chamber, then various concentrations (1 and 10 μM) of 3k were added to both chambers. After 12 h, non-invasive cells in the upper chamber were removed with a cotton swab, then fixed in paraformaldehyde and stained with 0.1% crystal violet. Photographs were taken using an inverted microscope and the cells were quantified manually to calculate the number of migrated cells.

Tube formation assay

Tube formation assay was performed as described previously28. Matrigel was put on ice overnight at 4 °C for the melt, and each well of a pre-chilled 96 well plate was coated with 60 μL Matrigel and then incubated at 37 °C for 30 min for the solidification. HUVECs (6000 cells) were premixed with various concentrations of 3k (5 and 20 μM) or Vandetanib and then seeded onto Matrigel. After 6 h of incubation at 37 °C with 5% CO2, the formation of HUVECs tubular structures was inspected under an OLYMPUS inverted microscope, and the percentage of tube formation inhibited by 3k was normalized to that of untreated control cells.

Ethics statement

The mice in the following experiments were maintained in the animal vivarium of East China Normal University, all of the experiments were performed in accordance with the approved guidelines and the protocols were approved by the Animal Investigation Committee of the East China Normal University.

Chick Embryo Chorioallantoic Membrane (CAM) Assay

CAM angiogenesis was assessed as described previously29. Fertilized chicken eggs were purchased from Shanghai Poultry Breeding Co. Ltd (Shanghai, China). Briefly, embryonic eggs were placed in a humidified incubator. After incubation for 5 days at 37 °C with 60% relative humidity, a 1–2 cm2 window was opened at the blunt end of the eggs and the shell membrane was removed to expose the CAM. Then, a 5 mm diameter filter paper disk with 5 or 20 μg of 3k, vandetanib or DMSO was placed on the CAM. Sealed the window and incubated the egg for 48 h to observe the result of neovascularization. The CAM microvessels were observed under a stereomicroscope, and the neovascularization was quantified using Image Pro Plus software.

Aortic Ring Spreading Assay

Aortic ring spreading assay was performed as previously described with minor modification30. 48-well plates were coated with 100 μL of Matrigel per well and polymerized at 37 °C for 30 min. Aortic rings harvested from 6 to 8-week-old Sprague-Dawley rats were plated in the wells and overlaid with 100 μL of Matrigel for sealing. VEGF (100 ng/mL) in serum-free culture medium, with or without different concentrations of compounds (1, 5, 10 and 20 μM) were added. The medium was changed every two days. Microvessel-like properties of sprouting structures were observed and photo-graphed on the 7th day and counted by Image-Pro Plus 6.0 software.

Xenograft Mouse Tumor Model

Xenograft model was prepared as described previously31. Male nude mice with 5–6 weeks old were inoculated subcutaneously in the right flank with 1 × 105 Bcap37 cells suspended in 50 μL of PBS. When tumor volume reached 130 mm3, mice were randomly assigned to the compound treatment group (n = 8) or the control (DMSO) group (n = 8). Compound 3k (30 mg/kg) was administered daily by intraperitoneal injection. Tumor volume was determined using digital vernier caliper measurements and the formula: A × B2 × 0.52, where A is the longest diameter of the tumor and B is the shortest diameter of the tumor.

Immunofluorescence assay

Immunofluorescence assay was performed as previously described32. HUVECs were cultured on gelatin-coated glass coverslips. After treatment with 3k (1, 5 and 20 μM) for indicated times, cells were fixed in 4% (w/v) paraformaldehyde for 30 min and permeabilized with 0.1% Triton-X100 in PBS for 5 min. F-actin and p-Paxillin was visualized by incubation with indicated antibody overnight at 4 °C (Cell Signaling Tech., Beverly, MA, USA) and then washed with PBS and incubated for 1 h with Alexa 488–conjugated secondary antibody (Jackson Immunoresearch Laboratories, West Grove, PA, USA). FITC-phalloidin and 4′, 6-diamidino-2-phenylindole (DAPI) were further used to stain F-actin and nuclei respectively. Photographs were obtained with a confocal microscope.

Western blot

Western blot assay was performed as previously described26. Whole cell lyastes were prepared in RIPA buffer supplemented with proteinase inhibitor cocktail (Roche, Basel, Switzerland). Cells were treated with 1, 5, 10 and 20 μM compound 3k for 24 h, then 50 ng/ml VEGF were added for 10 min before lysed. Lysates containing 40 mg of protein from each sample was subjected to SDS-polyacrylamide gel electrophoresis, transferred to PVDF membranes and blocked with 5% BSA. The membranes were then probed with indicated primary antibodies (p-FAK, FAK, p-Src, Src, p-JNK, JNK, p-c-Jun, c-Jun, p-ERK and ERK (Cell Signaling Tech., Beverly, MA, USA)), β-actin(Sigma, St. Louis, MO, USA) followed by incubation with horseradish peroxidase-conjugated goat anti-mouse or goat anti-rabbit antibody. The bound antibodies were detected using the ECL detection system.

Statistical analysis

Statistical analyses between the control and treatment groups were performed by standard two-tailed Student’s t-test. All experiments were repeated at least three times. Data were presented as means ± standard error. p values ≤ 0.05 were considered statistically significant. *p < 0.05; **p < 0.01; ***p < 0.001.

Chemistry

The general synthesis of substituted 4-methyl-2-(4-pyridinyl)thiazole-5-carboxamide analogs were demonstrated in Fig. 3. Substituted ethyl 4-methyl-2-(4-pyridinyl)thiazole-5-carboxylates 5 could be prepared from corresponding nitriles, followed by coupled with ethyl 2-bromoacetoacetate19,33, which were hydrolyzed to afford the intermediate 6, and then coupled with various amines to provide corresponding amide 3a−s in the presence of classic coupling reagents (Supplementary information).

Figure 3. Synthesis of compounds 3a−s.

Figure 3

Open in a new tab

Reagents and conditions: (A) LiOH·H2O, MeOH/H2O (B) amines, EDC·HCl, HOBt, anhydrous DMF.

Synthesis of 4a and 4b were illustrated in Fig. 4, which were similar with preparations of compounds 3a-s. Ethyl pyridinylthiazole carboxylates derivatives 7a and 7b were also synthesized following the similar routes for preparations of intermediates 534. Compounds 7a and 7b were hydrolyzed to afford 8a and 8b respectively, which were subsequently coupled with 3-methoxyphenyl amine in the presence of EDC·HCl and HOBt to provide target compounds 4a and 4b (Supplementary information).

Figure 4. Synthesis of compounds 4a,b.

Figure 4

Open in a new tab

Reagents and conditions: (A) LiOH·H2O, MeOH/H2O (B) 3-MeO-PhNH2, EDC·HCl, HOBt, anhydrous DMF.

Results and Discussion

Compounds inhibit colony formation of HUVECs

Colony formation not only can detect the adherent and proliferative cells, but also can confirm the ones with the ability to continue to proliferate and form colonies35. In order to well evaluate the abilities of synthesized compounds against HUVECs proliferation and development, colony formation assay was firstly performed to assess the efficacy of substituted 4-methyl-2-(4-pyridinyl)thiazole-5-carboxamides, and the FDA approved drug 1, a VEGFR2 inhibitor, was selected as a positive control36. At first, the aromaticity of substituents located in nitrogen atom of amide was investigated, as shown in Table 1. Compounds 3a-c with non-aromatic amide substitution showed weak or no inhibition of colony formation of HUVECs, with the IC50 values more than 20 μM, and introduction of phenylethyl group to amide would be resulted in a little bit increase of inhibiting colony formation effect, while compound 3e with phenyl amide substitution showed mild activity with IC50 of 9.0 ± 2.9 μM against colone formation of HUVECs.

Table 1. Inhibition of colon formation of HUVECs for compounds 3a−e.

graphic file with name srep33434-t1.jpg

Open in a new tab

Next, a series of different aromatic amines were coupled with 4-methyl-2-(4-pyridinyl)thiazole-5-carboxylic acid in order to generate more potent target compounds. The substitution positions were firstly examined for exploring the best one, and m-position substitution of phenyl at amide seemed to be the preferred one for increasing inhibitory effect (3g vs 3f and 3h) according to their colony formation effects against HUVECs in Table 2. However, the activity of compound 3i with bi-methoxy group substitutions at m-positions was not increased with an IC50 value of 6.9 ± 3.4 μM compared to mono-methoxy substituted analogue (3g). The substitutions of pyridinyl group were subsequently investigated, different groups, including some simple alkyl (3k–n) and benzyl (3o), were introduced to the pyridinyl ring, which verified that the substituent groups at this position were very important compared to no substitution (3j), and the compound 3k (IC50 = 2.1 ± 0.4 μM) with n-propyl group substitution showed best activities among these derivatives (3j–o) against HUVECs colony formation, which was comparable to 1 (IC50 = 1.6 ± 0.1 μM).

Table 2. Inhibition of cell colon formation of HUVECs for compounds 3e−s and 4a−b.

graphic file with name srep33434-t2.jpg

Open in a new tab

In addition, the anti-colony formation ability was also explored when the methoxy group at m-position of phenyl was further replaced by other different ones, such as chloro atom, nitro or amino group at the same position (3p–r). The results indicated that compounds with substitution of phenyl of methoxy replaced by electron-withdrawing groups would result in little difference (3k vs 3p,q) against colony formation. Compound 3s with tri-methoxy groups substitution at phenyl ring also showed a little bit decreased effect compared to the mono-methoxy group substituted analog (3k). Compound 4a was synthesized in order to further investigate the position of substitution of 3-methoxyphenyl amide and it was found that the change of substituted position led to obvious decrease toward the activities through comparing 3g with 4a. At last, compound 4b was further designed to examine whether bi-substitutions of 3-methoxyphenyl amide at 4- and 5-position of thiazole scaffold would resulted in the increasing inhibitory activities, which showed almost the best anti-colony formation activity, and even a little bit better than 1 among the investigated compounds.

Compounds inhibit the migration of HUVECs

As we know, the vascular endothelial cell layer can be regarded as a natural barrier against tumor cell trans-endothelial migration and invasion, which are one of the key steps in the process of a primary tumor growing to distant metastatic one37, therefore evaluation of the abilities of this series of compounds in inhibiting HUVECs migration maybe an effective and essential strategy for blocking tumor metastasis. Compounds 3k, 3m–r and 4b with good potency against colony formation (IC50 < 3 μM) were selected to further explore their activities against HUVECs migration with the model of wound-healing migration assay. As shown in Table 3 and Fig. 5, some of them showed better or comparable activities against HUVECs migration, especially for compound 3k, which showed almost one-fold better than 1 (IC50 = 3.4 ± 0.2 vs 6.0 ± 1.6 μM). In addition, the results also suggested that compounds with substitution of phenyl (R7) by electron-withdrawing groups (3p,q) would result in decreased anti-migration effect compared to those by electron-donating groups (3k,r). Unfortunately, compound 4b, with bi-substitutions of 3-methoxyphenyl amide at 4- and 5-position and showed best anti-colony formation efficacy among the investigated ones, was found to show weak anti-migration effect (IC50 = 22.4 ± 3.8 μM).

Table 3. Inhibition of migration of HUVECs for compounds 3k, 3m−r and 4b.

graphic file with name srep33434-t3.jpg

Open in a new tab
Figure 5. Target compounds inhibit HUVECs migration in a wound healing assay.

Figure 5

Open in a new tab

(A) Representative images of compounds inhibiting HUVECs migration with indicated concentrations. (B) The statistical results and IC50 values of target compounds against HUVECs migration. Values are means ± SD as determined by Student’s t test. **p < 0.01, ***p < 0.001.

In order to further investigate the efficacy of compound 3k against HUVECs migration, transwell assay was selected to perform the experiment, as shown in Fig. 6A,B, the results indicated that compound 3k definitely inhibited HUVECs invasion at the concentration of 1.0 μM. Given the activities of compound 3k against HUVECs colony formation and migration, it was chosen for further investigation ex vivo and in vivo.

Figure 6. Compound 3k inhibits HUVECs migration in a transwell assay and tube formation.

Figure 6

Open in a new tab

(A) Representative images of compounds inhibiting HUVECs migration in the transwell assay with different concentrations. (B) Migrated cells were quantified by manual counting. Values are means ± SD as determined by Student’s t test. **p < 0.01, ***p < 0.001. (C) Representative images of 3k or 1 (vandetanib) inhibiting HUVECs tube formation with different concentrations. (D) The quantitative data of tube formation assays. Values are means ± SD as determined by Student’s t test. **p < 0.01, ***p < 0.001.

Compound 3k inhibits tube formation in HUVECs

Endothelial cells spontaneously form three-dimensional capillary-like network on the matrigel in vitro, which is one of important steps in the process of angiogenesis38. To study the effects of compound 3k on tube formation of HUVECs, it was seeded with HUVECs onto the matrigel with different concentrations, and 1 was also chosen as the positive control. Their effects were examined through evaluating the efficacy of formation of capillary-like structure. As shown in Fig. 6C,D, the results indicated that 3k inhibited the ability of HUVECs to form capillary-like networks with a dose-dependent manner, and 5 μM of 3k inhibited almost 90% tube formation of HUVECs. These results further revealed 3k as a potential inhibitor of angiogenesis.

Compound 3k inhibits angiogenesis in the CAM assay

To directly examine the effects of 3k on angiogenesis and vascular development in vivo, a chick embryo chorioallantoic membrane (CAM) assay was performed, which is also the most widely used one to study angiogenesis39. Briefly, the shell membrane was removed from blunt end of embryonic eggs to expose the CAM. Then, a filter paper disk (5 mm diameter) with 5 μg or 20 μg of 3k, 1 or DMSO was placed on the CAM. The window was sealed and the egg was incubated for 48 h to observe the result of angiogenesis. According to the results listed in Fig. 7A,B, compound 3k inhibited the formation of new blood vessels branches in CAM assay with a reduction rate of 70% (5 μg/disc) and 80% (20 μg/disc), which was shown a comparable level with 1.

Figure 7. Anti-angiogenic activities of 3k ex vivo and in vivo.

Figure 7

Open in a new tab

(A) 3k inhibited the formation of new blood vessels branches in CAM assay. (B) The statistical results showed the percentage of inhibition was expressed using untreated group as 100%. Images were obtained with OLYMPUS stereomicroscope. (C) 3k inhibited VEGF-induced capillary-like micro-vessels from aortic ring. (D) The quantitation of micro-tube area. Values are means ± SD as determined by Student’s t test (n = 6, **p < 0.01; ***p < 0.001).

Compounds 3k inhibits microvessel formation in the rat aortic ring ex vivo

The aortic rings model of angiogenesis has been used widely to study new blood vessel formation40. Briefly, thoracic aortas from mice were dissected, sectioned and embedded in matrigel matrix and angiogenesis was stimulated by an angiogenesis-induced factor VEGF (100 ng/mL). Angiogenic sprouts (new vessels) can be visualized after 7 days41. Compounds 3k was selected for further investigation on a VEGF-induced angiogenesis of aortic ring assay model. The results was shown in Fig. 7C,D, compound 3k (IC50 = 6.3 μM) significantly suppressed the aortic ring sprouting. Therefore compound 3k was chosen for further evaluation in breast tumor growth and angiogenesis in vivo model.

Compound 3k inhibits tumor growth and angiogenesis in vivo

Tumor growth depends on angiogenesis because it provides necessary oxygen and nutrients for tumor. Based on the efficacy of compound 3k in HUVECs colony formation and migration, compound 3k was subsequently evaluated the tumor angiogenesis and tumor growth in mouse xenograft tumor model. As shown in Fig. 8, the tumors reached a volume of 130 mm3 after a 22 days’ subcutaneous injection of Bcap37 cells suspension into BALB/c mice, then the tumor-bearing mice were randomly divided into two groups (n = 8 for each group) and treated with 30 mg/kg of compound 3k or DMSO. The tumor weight and volume of the mice were dramatically suppressed when treated with compound 3k (Fig. 8A–C). At the same time, no significant difference of mice body weight was found between control and 3k-treated groups, which implied that the mice were tolerated to the 3k with the therapeutic dosage (Fig. 8D). Moreover, the number of vessels around the tumor was significantly decreased about 67% in compound 3k treated group compared with control group (Fig. 8E,F), partly indicated that compound 3k inhibited tumor growth mainly via anti-angiogenesis.

Figure 8. Compound 3k suppressed tumor growth and tumor angiogenesis.

Figure 8

Open in a new tab

(A–C) Photographs of tumor in DMSO and 3k treated group, along with the graph of tumor volume and tumor weight. (**p < 0.01; ***p < 0.001) (D) The average body weight between treated and untreated mouse groups. (E) Compound 3k inhibited angiogenesis around tumor. (F) The quantitation of angiogenesis. Values are means ± SD as determined by Student’s t test (n = 8, **p < 0.01; ***p < 0.001).

Compound 3k regulates the assignment of F-actin and p-Paxillin and affects angiogenesis signaling pathways in HUVECs

The above results have demonstrated that compound 3k inhibited the colony formation, migration and tube formation of HUVECs in vitro and suppressed neovascularization and tumor growth in vivo, possible mechanism was next explored about 3k. Cell migration is a pivotal step in angiogenesis. In endothelial cells, F-actin stress fibers and focal adhesions are working together to contribute to cell migration42. F–actin is essential for the cells to control and maintain their shape and morphological structure. Focal adhesions are multi-protein complexes that form mechanical links between intracellular actin bundles and extracellular matrix in which paxillin is an important adapter protein that control the dynamic change of focal adhesion assembly and disassembly43. F-actin and paxillin are of great importance in migration and angiogenesis, so the effect of 3k was examined on these proteins. As shown in Fig. 9A, 3k dose-dependently regulated F-actin filaments assignment, decreased the expression of p-paxillin and thus affected the shape of HUVECs. On the other hand, focal adhesion kinase (FAK) and Src are known as regulators of cell migration44, and activation of FAK and Src are regulated by mutual phosphorylation near the cell-matrix adhesion sites, which will leads to the formation of a co-activated FAK–Src complex45,46. The activated FAK–Src complex can mediate the phosphorylation of some well-known scaffold proteins like paxillin, which can connect extracellular matrices to the cytoskeleton and control the dynamic change of focal adhesion assembly and disassembly43. The effects of 3k were further explored on these cytoskeletal structure-related proteins. As shown in Fig. 9B, compound 3k decreased the VEGF-induced FAK and Src phosphorylation in a dose-dependent manner, which suggested that compound 3k inhibited cell spreading through the suppression effect on FAK-Src and Paxillin.

Figure 9.

Figure 9

Open in a new tab

(A) Compound 3k regulated the F-actin stress fiber assignment (upper, red) and decreased the expression of p-Paxillin (lower, green) in HUVECs. (B) Compound 3k remarkably inhibited VEGF-induced phosphorylation of FAK and Src.

The two main MAP kinases extracellular signal-regulated kinase (ERK) and c-Jun N-terminal kinase (JNK) regulate distinct cellular activities even though they share some common substrates such as c-jun, which is an inducible transcription factor directs gene expression in response to multiple extracellular stimuli47. ERK has been implicated in the regulation of angiogenesis for various functions including cell proliferation, migration, and survival48. JNK mediates signal transduction from cell surface receptors to the nucleus and regulating programmed cell death by modulating some anti-apoptotic proteins49. Next compound 3k was examined whether it can regulate the activation of ERK and JNK in HUVECs. As shown in Fig. 10A, compound 3k produced a dose–dependent inhibition of VEGF-stimulated phosphorylation of ERK, JNK and c-Jun. These results confirmed our hypothesis that 3k inhibited angiogenesis via blocking the MAPK pathway. Together, these data indicated that compound 3k exerts its antiangiogenic functions mainly by blocking angiogenesis signaling pathways (Fig. 10B).

Figure 10.

Figure 10

Open in a new tab

(A) Compound 3k inhibited downstream proteins phosphorylation (p-ERK, p-JNK, p-c-jun). (B) Proposed model of 3k function in inhibiting tumor angiogenesis and tumor growth.

Conclusions

With the aim of developing novel inhibitors of angiogenesis for the treatment of tumor growth and metastasis, a series of novel N-Substituted 2-(4-pyridinyl)thiazole carboxamides were designed, synthesized and their inhibitory effects were explored against colony formation and migration of HUVECs in vitro. Detailed SAR analysis and structural optimization resulted in the discovery of N-(3-methoxyphenyl)-4-methyl-2-(2-propyl-4-pyridinyl)thiazole-5-carboxamide (3k). In subsequent studies, compound 3k was found to inhibit angiogenesis by suppressing key angiogenic steps including transwell migration, tube formation of endothelial cells in vitro and microvessel formation ex vivo. Next the effects of compound 3k against angiogenesis and tumor growth were also verified in a VEGF-induced angiogenesis in the mouse corneal neovascularization model in vivo. In addition, Compound 3k also showed excellent effect with the dosage of 30 mg/kg on a breast tumor growth model. Further investigations indicated that compound 3k could be functioned as a tumor angiogenesis inhibitor mainly by the suppression of angiogenesis signaling pathways, such as ERK, JNK and FAK-Src etc. Therefore this series of new compounds may be effective in developing novel strategies for future cancer treatment.

Additional Information

How to cite this article: Zhou, W. et al. Discovery and Optimization of N-Substituted 2-(4-pyridinyl)thiazole carboxamides against Tumor Growth through Regulating Angiogenesis Signaling Pathways. Sci. Rep. 6, 33434; doi: 10.1038/srep33434 (2016).

Supplementary Material

Supplementary Information
srep33434-s1.doc (2.5MB, doc)

Acknowledgments

This work was supported by the grants from National Basic Research Program of China (2012CB910404 and 2015CB910400), National Natural Science Foundation of China (81673304, 81272463 and 81472788), The Science and Technology Commission of Shanghai Municipality (15431902200), Research Fund for the Doctoral Program of Higher Education of China (20120076120029) and Shanghai Fengxian District Science and Technology Project (20141001).

Footnotes

Author Contributions W.Z., W.T., Y.L. and Y.D. performed the research. Y.C., Z.Y., Z.S. and W.Z. designed the research study. H.P., Y.P., J.W., Z.J. and T.S. contributed essential reagents or tools. W.Z., Y.P., Z.J. and Y.C. analyzed the data. W.Z., W.T., Z.S., Z.Y. and Y.C. wrote the paper.

References

  1. Qin J., Chen X., Xie X., Tsai M. J. & Tsai S. Y. COUP-TFII regulates tumor growth and metastasis by modulating tumor angiogenesis. Proc Natl Acad Sci USA 107, 3687–3692, doi: 10.1073/pnas.0914619107 (2010). [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Folkman J. Angiogenesis in cancer, vascular, rheumatoid and other disease. Nature medicine 1, 27–31 (1995). [DOI] [PubMed] [Google Scholar]
  3. Carmeliet P. & Jain R. K. Angiogenesis in cancer and other diseases. Nature 407, 249–257, doi: 10.1038/35025220 (2000). [DOI] [PubMed] [Google Scholar]
  4. Lechertier T., Berard M., Vassy R., Herve M. A. & Crepin M. Transendothelial migration of two metastatic breast carcinoma cells depend on the SDF-lalpha-CXCR4 complexes. Anticancer research 24, 4011–4017 (2004). [PubMed] [Google Scholar]
  5. Kerbel R. & Folkman J. Clinical translation of angiogenesis inhibitors. Nature reviews. Cancer 2, 727–739, doi: 10.1038/nrc905 (2002). [DOI] [PubMed] [Google Scholar]
  6. Folkman J. Angiogenesis. Annual review of medicine 57, 1–18, doi: 10.1146/annurev.med.57.121304.131306 (2006). [DOI] [PubMed] [Google Scholar]
  7. Folkman J. Angiogenesis: an organizing principle for drug discovery? Nature reviews. Drug discovery 6, 273–286, doi: 10.1038/nrd2115 (2007). [DOI] [PubMed] [Google Scholar]
  8. Kerbel R. S. et al. Possible mechanisms of acquired resistance to anti-angiogenic drugs: implications for the use of combination therapy approaches. Cancer metastasis reviews 20, 79–86 (2001). [DOI] [PubMed] [Google Scholar]
  9. Gasparini G., Longo R., Toi M. & Ferrara N. Angiogenic inhibitors: a new therapeutic strategy in oncology. Nature clinical practice. Oncology 2, 562–577, doi: 10.1038/ncponc0342 (2005). [DOI] [PubMed] [Google Scholar]
  10. Ferrara N., Hillan K. J., Gerber H. P. & Novotny W. Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer. Nature reviews. Drug discovery 3, 391–400, doi: 10.1038/nrd1381 (2004). [DOI] [PubMed] [Google Scholar]
  11. Aziz M. A. et al. Discovery of Potent VEGFR-2 Inhibitors based on Furopyrimidine and Thienopyrimidne Scaffolds as Cancer Targeting Agents. Scientific reports 6, 24460, doi: 10.1038/srep24460 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Cryan L. M. et al. 1,2,3,4,6-Penta-O-galloyl-beta-D-glucopyranose inhibits angiogenesis via inhibition of capillary morphogenesis gene 2. J Med Chem 56, 1940–1945, doi: 10.1021/jm301558t (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Ferro V. et al. Discovery of PG545: a highly potent and simultaneous inhibitor of angiogenesis, tumor growth, and metastasis. J Med Chem 55, 3804–3813, doi: 10.1021/jm201708h (2012). [DOI] [PubMed] [Google Scholar]
  14. Johnstone K. D. et al. Synthesis and biological evaluation of polysulfated oligosaccharide glycosides as inhibitors of angiogenesis and tumor growth. J Med Chem 53, 1686–1699, doi: 10.1021/jm901449m (2010). [DOI] [PubMed] [Google Scholar]
  15. Marin-Ramos N. I. et al. New Inhibitors of Angiogenesis with Antitumor Activity in Vivo. J Med Chem 58, 3757–3766, doi: 10.1021/jm5019252 (2015). [DOI] [PubMed] [Google Scholar]
  16. Lu Y. et al. Design, synthesis, and SAR studies of 4-substituted methoxylbenzoyl-aryl-thiazoles analogues as potent and orally bioavailable anticancer agents. J Med Chem 54, 4678–4693, doi: 10.1021/jm2003427 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lu Y. et al. Discovery of 4-substituted methoxybenzoyl-aryl-thiazole as novel anticancer agents: synthesis, biological evaluation, and structure-activity relationships. J Med Chem 52, 1701–1711, doi: 10.1021/jm801449a (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Zheng S. et al. Modification and biological evaluation of thiazole derivatives as novel inhibitors of metastatic cancer cell migration and invasion. J Med Chem 57, 6653–6667, doi: 10.1021/jm500724x (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Zhou W. et al. Design and optimization of hybrid of 2,4-diaminopyrimidine and arylthiazole scaffold as anticancer cell proliferation and migration agents. Eur J Med Chem 96, 269–280, doi: 10.1016/j.ejmech.2015.04.027 (2015). [DOI] [PubMed] [Google Scholar]
  20. Suzuki T. et al. Novel inhibitors of human histone deacetylases: design, synthesis, enzyme inhibition, and cancer cell growth inhibition of SAHA-based non-hydroxamates. J Med Chem 48, 1019–1032, doi: 10.1021/jm049207j (2005). [DOI] [PubMed] [Google Scholar]
  21. Hay M. P. et al. 4-Pyridylanilinothiazoles that selectively target von Hippel-Lindau deficient renal cell carcinoma cells by inducing autophagic cell death. J Med Chem 53, 787–797, doi: 10.1021/jm901457w (2010). [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Qiu X. L. et al. Synthesis and biological evaluation of a series of novel inhibitor of Nek2/Hec1 analogues. J Med Chem 52, 1757–1767, doi: 10.1021/jm8015969 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Kamisuki S. et al. Synthesis and evaluation of diarylthiazole derivatives that inhibit activation of sterol regulatory element-binding proteins. J Med Chem 54, 4923–4927, doi: 10.1021/jm200304y (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Yang F. et al. Design and optimization of novel hydroxamate-based histone deacetylase inhibitors of bis-substituted aromatic amides bearing potent activities against tumor growth and metastasis. J Med Chem 57, 9357–9369, doi: 10.1021/jm5012148 (2014). [DOI] [PubMed] [Google Scholar]
  25. Zheng C. et al. Synthesis and biological evaluation of novel tetrahydro-beta-carboline derivatives as antitumor growth and metastasis agents through inhibiting the transforming growth factor-beta signaling pathway. J Med Chem 57, 600–612, doi: 10.1021/jm401117t (2014). [DOI] [PubMed] [Google Scholar]
  26. Pang X. et al. Morelloflavone, a biflavonoid, inhibits tumor angiogenesis by targeting rho GTPases and extracellular signal-regulated kinase signaling pathways. Cancer research 69, 518–525, doi: 10.1158/0008-5472.CAN-08-2531 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Song J. et al. miR-34c-3p inhibits cell proliferation, migration and invasion of hepatocellular carcinoma by targeting MARCKS. International journal of clinical and experimental pathology 8, 12728–12737 (2015). [PMC free article] [PubMed] [Google Scholar]
  28. Yi T. et al. Gambogic acid inhibits angiogenesis and prostate tumor growth by suppressing vascular endothelial growth factor receptor 2 signaling. Cancer research 68, 1843–1850, doi: 10.1158/0008-5472.CAN-07-5944 (2008). [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Lai L. et al. Plumbagin inhibits tumour angiogenesis and tumour growth through the Ras signalling pathway following activation of the VEGF receptor-2. British journal of pharmacology 165, 1084–1096, doi: 10.1111/j.1476-5381.2011.01532.x (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Dai F. et al. A natural small molecule harmine inhibits angiogenesis and suppresses tumour growth through activation of p53 in endothelial cells. PloS one 7, e52162, doi: 10.1371/journal.pone.0052162 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Chen J. et al. Inhibition of STAT3 signaling pathway by nitidine chloride suppressed the angiogenesis and growth of human gastric cancer. Molecular cancer therapeutics 11, 277–287, doi: 10.1158/1535-7163.MCT-11-0648 (2012). [DOI] [PubMed] [Google Scholar]
  32. Song Y. J. et al. Usnic acid inhibits breast tumor angiogenesis and growth by suppressing VEGFR2-mediated AKT and ERK1/2 signaling pathways. Angiogenesis 15, 421–432, doi: 10.1007/s10456-012-9270-4 (2012). [DOI] [PubMed] [Google Scholar]
  33. Li G. et al. Identification, synthesis and photo-protection evaluation of arylthiazole derivatives as a novel series of sunscreens. Heterocycles 89, 453–464 (2014). [Google Scholar]
  34. Guo J. et al. An efficient synthesis of a potent PPARpan agonist. The Journal of organic chemistry 71, 8302–8305, doi: 10.1021/jo061295n (2006). [DOI] [PubMed] [Google Scholar]
  35. Sun D., Yang K., Zheng G., Li Z. & Cao Y. Study on effect of peptide-conjugated near-infrared fluorescent quantum dots on the clone formation, proliferation, apoptosis, and tumorigenicity ability of human buccal squamous cell carcinoma cell line BcaCD885. International journal of nanomedicine 5, 401–405 (2010). [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Inoue K. et al. Vandetanib, an inhibitor of VEGF receptor-2 and EGF receptor, suppresses tumor development and improves prognosis of liver cancer in mice. Clinical cancer research: an official journal of the American Association for Cancer Research 18, 3924–3933, doi: 10.1158/1078-0432.CCR-11-2041 (2012). [DOI] [PubMed] [Google Scholar]
  37. Longo N. et al. Regulatory role of tetraspanin CD9 in tumor-endothelial cell interaction during transendothelial invasion of melanoma cells. Blood 98, 3717–3726 (2001). [DOI] [PubMed] [Google Scholar]
  38. Tozer G. M., Kanthou C. & Baguley B. C. Disrupting tumour blood vessels. Nature reviews. Cancer 5, 423–435, doi: 10.1038/nrc1628 (2005). [DOI] [PubMed] [Google Scholar]
  39. Ribatti D. et al. Lipoprotein (a) induces angiogenesis on the chick embryo chorioallantoic membrane. European journal of clinical investigation 28, 533–537 (1998). [DOI] [PubMed] [Google Scholar]
  40. Baker M. et al. Use of the mouse aortic ring assay to study angiogenesis. Nature protocols 7, 89–104, doi: 10.1038/nprot.2011.435 (2012). [DOI] [PubMed] [Google Scholar]
  41. De Rossi G., Scotland R. & Whiteford J. Critical Factors in Measuring Angiogenesis Using the Aortic Ring Model. Journal of genetic syndromes & gene therapy 4, pii: 1000147, doi: 10.4172/2157-7412.1000147 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Lamalice L., Le Boeuf F. & Huot J. Endothelial cell migration during angiogenesis. Circulation research 100, 782–794, doi: 10.1161/01.RES.0000259593.07661.1e (2007). [DOI] [PubMed] [Google Scholar]
  43. Grimsley C. M. et al. Dock180 and ELMO1 proteins cooperate to promote evolutionarily conserved Rac-dependent cell migration. J Biol Chem 279, 6087–6097, doi: 10.1074/jbc.M307087200 (2004). [DOI] [PubMed] [Google Scholar]
  44. Bianchi-Smiraglia A., Paesante S. & Bakin A. V. Integrin beta5 contributes to the tumorigenic potential of breast cancer cells through the Src-FAK and MEK-ERK signaling pathways. Oncogene 32, 3049–3058, doi: 10.1038/onc.2012.320 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Sulzmaier F. J., Jean C. & Schlaepfer D. D. FAK in cancer: mechanistic findings and clinical applications. Nature reviews. Cancer 14, 598–610, doi: 10.1038/nrc3792 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Sen B. & Johnson F. M. Regulation of SRC family kinases in human cancers. Journal of signal transduction 2011, 865819, doi: 10.1155/2011/865819 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Leppa S., Saffrich R., Ansorge W. & Bohmann D. Differential regulation of c-Jun by ERK and JNK during PC12 cell differentiation. Embo Journal 17, 4404–4413, doi: 10.1093/emboj/17.15.4404 (1998). [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Risau W. Mechanisms of angiogenesis. Nature 386, 671–674, doi: 10.1038/386671a0 (1997). [DOI] [PubMed] [Google Scholar]
  49. Mishra O. P., Zubrow A. B. & Ashraf Q. M. Nitric oxide-mediated activation of extracellular signalregulated kinase (ERk) and c-Jun n-Terminal kinase (JNK) during hypoxia in cerebral cortical nuclei of newborn piglets. Neuroscience 123, 179–186, doi: 10.1016/j.neuroscience.2003.08.008 (2004). [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary Information
srep33434-s1.doc (2.5MB, doc)

Articles from Scientific Reports are provided here courtesy of Nature Publishing Group

RESOURCES