Shikonin suppresses proliferation and induces apoptosis in human leukemia NB4 cells through modulation of MAPKs and c-Myc

Abstract

Acute promyelocytic leukemia (APL) is a special subtype of acute myeloid leukemia that responds to treatment with all-trans retinoic acid and arsenic trioxide. However, severe side effects and drug resistance limit the effectiveness of these treatments. Hence, new drugs for APL are required urgently. Shikonin, an active naphthoquinone derived from the Chinese medical herb Zi Cao exerts antitumor activity in several cancers. In the present study, the effects of shikonin on proliferation and apoptosis in NB4 cells, as well as related mechanisms were assessed. Treatment of NB4 cells with shikonin inhibited proliferation in a concentration- and time-dependent manner. The cell cycle was arrested in the G1 phase. NB4 cells treated with shikonin exhibited more apoptosis and higher levels of cleaved caspase-3 and poly ADP-ribose polymerase than control cells. Western blotting results demonstrated that the expression of p-p38 mitogen-activated protein kinase (p-p38MAPK) and p-c-Jun N-terminal kinase (p-JNK) was increased significantly by shikonin treatment, while the expression of p-ERK and c-Myc was decreased. In summary, these findings indicated that shikonin inhibited cell proliferation and induced apoptosis partly through modulation of the MAPKs and downregulation of c-Myc.

Introduction

Acute promyelocytic leukemia (APL) is a subtype of acute myeloid leukemia accounting for 5–15% of all forms of this disease (1). APL is characterized by a chromosomal translocation [t(15;17)(q24;q21)] resulting in the formation of a retinoic acid receptor α and promyelocytic leukemia (PML-RARα) fusion protein (1–3). All-trans retinoic acid (ATRA) and arsenic trioxide (ATO) are the most important treatments of APL patients and induce a high cure rate. ATRA promotes differentiation and ATO induces apoptosis. Although ATRA and ATO have made APL highly curable, some patients may develop severe side effects. In addition, some APL patients are not sensitive to these compounds (1,4–7). Hence, it is necessary to develop new therapeutic strategies for this disease.

Shikonin, an active component of the Chinese medical herb Zi Cao has been used to treat burns, carbuncles, macular eruptions, measles and sore throats (8,9). In addition to the anti-bacterial and anti-inflammatory activities of this medicine, shikonin inhibits proliferation and induces apoptosis in different cancer cell lines including prostate cancer (10), oral squamous cell carcinoma (11), chronic myelogenous leukemia (12), hepatocellular carcinoma (13) and thyroid cancer (14). Substantial evidence indicates that shikonin induces apoptosis partly through the mitogen-activated protein kinase (MAPK) pathway (12,15).

The MAPK family, that includes extracellular signal-regulated kinase (ERK), p38 MAPK and c-Jun N-terminal kinase (JNK), serves an important role in cell proliferation, cell cycle progression, differentiation, survival and apoptosis (16,17). The ERK pathway is primarily activated by growth factors and mitogens, and is important in cell growth and differentiation (18). p38 MAPK and JNK are mainly responsive to stress signals and inflammatory cytokines, and are associated with apoptosis (19,20).

Accumulating evidence indicates that shikonin exerts antitumor activity in different cancer cells. However, the effects and related mechanism of shikonin on human leukemia NB4 cells are not known. In the present study, the authors investigated the influence of shikonin on the proliferation and apoptosis of NB4 cells and explored the potential mechanisms. The results may be beneficial for developing improved therapies for APL.

Materials and methods

Reagents

Shikonin and dimethylsulfoxide were purchased from Sigma-Aldrich; Merck KGaA, Darmstadt, Germany). The purity of shikonin was >98%. Antibodies against caspase-3, poly ADP-ribose polymerase (PARP), c-Myc, p-ERK1/2, ERK1/2, p38 MAPK, p-JNK and JNK were purchased from Cell Signaling Technology, Inc. (Danvers, MA, USA). The antibody against p-p38 MAPK was purchased from Merck KGaA. Goat anti-rabbit, goat anti-mouse and β-actin antibodies were purchased from Beijing Zhongshan Golden Bridge Biotechnology Co., Ltd. (Beijing, China).

Cell lines and culture

NB4 cells were obtained from the Shanghai Institute for Biological Science, Chinese Academy of Sciences (Shanghai, China) and maintained at 37°C under 5% CO₂ in RPMI-1640 (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) medium containing 10% fetal calf serum (Gibco; Thermo Fisher Scientific, Inc.).

Cell proliferation assays

Cell viability was detected by the Cell Counting Kit (CCK)-8 (Sevenseas Futai Biotechnology Co., Ltd., Shanghai, China) assay. Cells (1×10⁴) were seeded in 96-well plates and treated with increasing concentrations of shikonin for 12, 24 and 36 h. A total of 10 µl CCK-8 solution was added to each well at the end of each culture period. Cells were then incubated for 2 h at 37°C and absorbance of the medium was measured at 450 nm using a spectrophotometer.

Nucleus morphological changes examined by Hochest 33342 staining

Cells (5×10⁵) were seeded in six-well plates and treated with shikonin (0, 0.3 µmol/l) for 24 h. Then, cells were washed with PBS three times, fixed with cold methanol overnight. Cells were washed with PBS three further times and stained with Hoechst 33342 (Beyotime Institute of Biotechnology, Beijing, China) for 5 min in the dark. Following three washes, the cells were observed using fluorescence microscopy.

Flow cytometry analysis

NB4 cells were treated with 0.3 µmol/l shikonin for 24 h. Treated and control cells were harvested by centrifugation at 1,000 × g for 5 min then washed and re-suspended with cold PBS. Cells were then stained with Annexin V and propidium iodide for 5–15 min at room temperature using the Annexin V/PI Apoptosis Detection kit (KeyGene, Wageningen, The Netherlands). Apoptosis was analyzed on a flow cytometer (BD Biosciences, Franklin Lakes, NJ, USA). The experiment was repeated at least three times.

The effects of shikonin on cell cycle distribution were detected with a cell cycle kit according to the manufacturer's instructions. Cells treated with 0.3 µmol/l shikonin for 24 h and control cells were collected by centrifugation, followed by washing, fixation and propidium iodide staining. The cell cycle distribution was examined by flow cytometry (BD Biosciences).

Western blot analyses

Cells were lysed with cold radioimmunoprecipitation assay lysis buffer (Beyotime Institute of Biotechnology) containing protease inhibitor cocktail for 10 min. Cell proteins were collected by centrifuging at 13,000 × g for 30 min and used for immunoblotting analyses. Cell proteins (60 µg) were separated by SDS-PAGE and transferred to polyvinylidene fluoride membranes (EMD Millipore, Billerica, MA, USA). The membranes were blocked with 5% non-fat milk dissolved in TBS with 20% Tween-20, and then incubated with primary antibodies against caspase-3 (no. 9665; 1:1,000), PARP (no. 9532; 1:1,000), c-Myc (no. 5605; 1:1,000), p-ERK1/2 (no. 4370; 1:1,000), ERK1/2 (no. 4695; 1:1,000), p-p38 MAPK (no. 09-272; 1:1,000), p38 MAPK (no. 9218; 1:1,000), p-JNK (no. 4668; 1:1,000), JNK (no. 9252; 1:1,000), β-actin (no. BM0627; 1:4,000) at 4°C overnight. Following three washes, the membranes were incubated with goat anti-rabbit (no. ZB-2301; 1:4,000) or goat anti-mouse (no. ZB-2305; 1:4,000) IgG horseradish peroxidase-linked secondary antibodies, at room temperature for 1 h. The bands were visualized using Immobilon Western Chemiluminescent HRP Substrate (EMD Millipore). Semi-quantification was performed using Cool Imager software (version. 4.0.1; Viagen Biotech Inc., Los Angeles, CA, USA).

Statistical analysis

All experiments were repeated at least three times. Data are presented as means ± standard deviation. Statistical analysis was performed with SPSS software (version, 17.0; SPSS, Inc., Chicago, IL, USA). One-way analysis of variance and Student's t-test were used for comparisons. P<0.05 was considered to indicate a statistically significant difference.

Results

Shikonin inhibits the proliferation of NB4 cells

NB4 cells were treated with increasing concentrations of shikonin for 24 h and viability assessed using the CCK-8 assay. There was no significant difference between the control and shikonin 0.1 µmol/l group in cell viability (Fig. 1A). However, cell viability was reduced significantly by treatment with shikonin concentrations of 0.2 µmol/l or more. The IC₅₀ value was 0.3 µmol/l. NB4 cells were also treated with 0.3 µmol/l shikonin for 0–36 h. The CCK-8 results demonstrated that this treatment reduced cell viability significantly from 12–36 h (Fig. 1B). These results indicated that shikonin inhibited the viability of NB4 cells in a concentration- and time-dependent manner.

Figure 1.

Treatment with shikonin inhibited human leukemia NB4 cell proliferation. (A) NB4 cells were treated with 0.1–0.4 µmol/l shikonin for 24 h. **P<0.01 vs. 0 µmol/l shikonin. (B) NB4 cells were treated with 0.3 µmol/l shikonin for 12, 24 and 36 h. CCK-8 results demonstrated that shikonin inhibited NB4 cells growth in dose and time-dependent manner. *P<0.05, **P<0.01 vs. time 0.

Nucleus morphological changes observed by fluorescence micsroscopy

The cell nuclei of untreated NB4 cells stained by Hoechst 33342 were round and uniform, while shikonin treatment resulted in chromatin agglutination, karyopyknosis and nuclear fragmentation (Fig. 2).

Figure 2.

Effect of shikonin on nuclear morphology of NB4 cells was observed by florescence microscopy (magnification, ×400). DMSO, dimethylsulfoxide.

Shikonin-induced cell cycle changes

NB4 cells were treated with 0.3 µmol/l shikonin for 24 h and the cell cycle was detected by flow cytometry. Compared with the control group, shikonin-treated cells were arrested at the G1 phase. The percentage of cells in the G1 phase increased from 37.3 to 51.8% (Fig. 3). This result indicated that shikonin induced cell cycle arrest of NB4 cells.

Figure 3.

Changes in the cell cycle distribution in NB4 cells. (A) Treatment of 0.3 µmol/l shikonin in NB4 cells for 24 h induced the cell cycle arrest in the G1 phase. (B) Quantification of these data. ^##P<0.01 vs. blank control; **P<0.01 vs. DMSO. DMSO, dimethylsulfoxide.

Shikonin induced apoptosis of NB4 cells

The effect of 0.3 µmol/l shikonin on NB4 cell apoptosis was detected by flow cytometry at 24 h. The percentage of apoptosis cell was increased significantly by shikonin treatment (Fig. 4).

Figure 4.

Shikonin increased NB4 cells apoptosis. (A) NB4 cells were treated with 0.3 µmol/l shikonin for 24 h, then cell apoptosis was detected by flow cytometry. The percentage of apoptosis cells was increased by shikonin treatment. (B) Quantification of these data. **P<0.01 vs. control. DMSO, dimethylsulfoxide; FITC, fluorescein isothiocyanate.

Shikonin increased the expression levels of cleaved PARP and caspase-3

Western blotting was used to detect the apoptosis-related proteins PARP and caspase-3. The expression of cleaved PARP and caspase-3 was increased following treatment with 0.3 µmol/l shikonin for 24 h, as compared with the control group (Fig. 5), supporting the induction of apoptosis by this treatment.

Figure 5.

Effect of shikonin on the expression levels of apoptosis related proteins. (A) NB4 cells were treated with 0.3 µmol/l shikonin for 24 h. The expression levels of cleaved caspase-3 and cleaved PARP were increased. The expression levels of caspase-3 and PARP were not changed. (B) Quantification analysis of western blotting. **P<0.01 vs. control. PARP, poly ADP-ribose polymerase.

Shikonin regulated MAPKs and downregulated c-Myc in NB4 cells

To investigate possible mechanisms for shikonin-induced apoptosis in NB4 cells, the authors assessed the levels of MAPKs and the expression of c-Myc. Shikonin increased the phosphorylation of p38 MAPK and JNK significantly, and inhibited ERK phosphorylation (Fig. 6). However, the expression of total ERK, p38 MAPK and JNK was not affected by shikonin. Meanwhile, the expression of c-Myc was significantly decreased by treatment with shikonin.

Figure 6.

Effect of shikonin on the expression of mitogen-associated protein kinases and c-Myc. (A-D) NB4 cells were treated with 0.3 µmol/l shikonin for 24 h, and protein expression was measured by western blotting. (E-H) Quantification analysis of western blotting. *P<0.05, **P<0.01 vs. control. JNK, Jun N-terminal kinase; ERK, extracellular signal-regulated kinase.

Discussion

Shikonin, a natural product derived from the Chinese medical herb Zi Cao, has been used for treating wounds and burns, and has anti-inflammatory and anti-viral properties (8,9). Previously, evidence has indicated that shikonin exerts antitumor activity by inhibiting cell proliferation and inducing apoptosis in different tumor cell lines (10–14). However, little is known about the effects of shikonin on human leukemia NB4 cells.

In the present study, the authors firstly investigated the effects of shikonin on proliferation and apoptosis in NB4 cells. The results demonstrated that shikonin inhibited the proliferation of NB4 cells in a time- and concentration-dependent manner and induced cell cycle arrest in the G1 phase. The percentage of apoptotic cells was increased significantly following shikonin treatment. Shikonin treatment led to nucleus morphological changes such as chromatin agglutination, karyopyknosis and nuclear fragmentation. These results indicated that shikonin could inhibit the proliferation and induce apoptosis in NB4 cells. The study used NB4 cells because it is the primary cell type with the APL containing PML-RARα fusion protein. In addition, the effects of shikonin on normal healthy cells were not explored because of the difficulty of culturing normal blood cells. Western blotting analyses indicated that shikonin treatment increased the cleaved caspase-3 and PARP, two apoptosis-related proteins. Furthermore, shikonin can generate reactive oxygen species and active caspases to induce apoptosis in human colorectal carcinoma cells (21). Apoptosis signal transduction involves the death receptor and mitochondrial pathways (22). In order to explore the molecular mechanism underlying the antitumor activity of shikonin, we measured its effects on cell proliferation and apoptosis signaling pathways. Studies reported that MAPK signaling pathway closely related to proliferation and apoptosis (16,17). Modulation of the p38 MAPK and JNK pathways often associated with apoptosis, and the ERK pathway always related to cell survival (23–25). Western blotting examined the p38 MAPK, JNK and ERK pathways. In addition, the expression of c-Myc, an oncogene that serves an important role in cell proliferation, differentiation and apoptosis (26), and is overexpressed in many cancer cells (27), was examined. c-Myc can promote the PARP-dependent DNA repair pathway resulting in chemoresistance (28). In addition, a previous study reported that shikonin induces apoptosis by downregulating c-Myc in U937 cells (15). The current results are consistent with previous findings. Total MAPKs were unaffected by shikonin treatment. However, shikonin inhibited the expression of p-ERK and increased levels of p-p38 MAPK and p-JNK. Meanwhile, c-Myc was significantly downregulated by shikonin. These results indicated that shikonin-induced apoptosis may be through the MAPK pathway and downregulation of c-Myc in NB4 cells. However, further investigations are needed to identify how these pathways are regulated and their relationship to each other and to investigate the effects of Shikonin in animal models of APL.

In conclusion, the current study indicated that shikonin inhibited cell proliferation and induced cell cycle arrest and apoptosis in NB4 cells. These effects involved modulation of the MAPK pathway and downregulation of c-Myc. These results suggested that shikonin may be a novel agent for treating APL.