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World Journal of Gastroenterology logoLink to World Journal of Gastroenterology
. 2018 Mar 14;24(10):1072–1083. doi: 10.3748/wjg.v24.i10.1072

Narrow line between benefit and harm: Additivity of hyperthermia to cisplatin cytotoxicity in different gastrointestinal cancer cells

Vaidotas Cesna 1, Arturas Sukovas 2, Aldona Jasukaitiene 3, Rima Naginiene 4, Giedrius Barauskas 5, Zilvinas Dambrauskas 6, Saulius Paskauskas 7, Antanas Gulbinas 8
PMCID: PMC5850127  PMID: 29563752

Abstract

AIM

To investigate the response to hyperthermia and chemotherapy, analyzing apoptosis, cytotoxicity, and cisplatin concentration in different digestive system cancer cells.

METHODS

AGS (gastric cancer cell line), Caco-2 (colon cancer cell line) and T3M4 (pancreatic cancer cell line) were treated by cisplatin and different temperature setting (37 °C to 45 °C) either in isolation, or in combination. Treatment lasted for one hour. 48 h after the treatment viability was evaluated by MTT, cell apoptosis by Annexin V-PE and 7ADD flow cytometry. Intracellular cisplatin concentration was measured immediately after the treatment, using mass spectrometry. Isobologram analysis was performed to evaluate the mathematical combined effect of temperature and cisplatin.

RESULTS

AGS cells were the most sensitive to isolated application of hyperthermia. Hyperthermia, in addition to cisplatin treatment, did not provoke a synergistic effect at intervals from 37 °C to 41 °C in neither cancer cell line. However, a temperature of 43 °C enhanced cisplatin cytotoxicity for Caco-2 cells. Moreover, isobologram analysis revealed mathematical antagonistic effects of cisplatin and temperature combined treatment in AGS cells; variations between synergistic, additive, and antagonistic effects in Caco-2 cells; and additive and antagonistic effects in T3M4 cells. Combined treatment enhanced initiation of cell apoptosis in AGS, Caco-2, and T3M4 cells by 61%, 20%, and 19% respectively. The increase of intracellular cisplatin concentration was observed at 43 °C by 30%, 20%, and 18% in AGS, Caco-2, and T3M4 cells, respectively.

CONCLUSION

In addition to cisplatin, hyperthermia up to 43 °C does not affect the viability of cancer cells in a synergistic manner.

Keywords: Hyperthermal intraperitoneal chemotherapy, Cisplatin, Hyperthermia, Isobolograms, Gastric cancer, Pancreatic cancer, Colon cancer

Core tip: Hyperthermal intraperitoneal chemotherapy is widely used as a standard treatment option for peritoneum invading gastrointestinal cancer. Our in vitro results suggest that optimal temperature has to be taken into consideration for achieving optimal therapeutic effect. In addition to cisplatin, hyperthermia up to 43 °C does not affect the viability of AGS, Caco-2, and T3M4 cells in a synergistic manner. However, some regimens of hyperthermia and cisplatin treatment are beneficial regarding an increase in intracellular cisplatin concentration and enhancement apoptosis of gastrointestinal cancer cells.

INTRODUCTION

For the past two decades, hyperthermal intraperitoneal chemotherapy (HIPEC) has been considered as a treatment option for peritoneum invading gastrointestinal cancers[1]. Various studies have demonstrated improved survival rates for gastric[2] and colorectal cancers[3-5]. The clinical application of hyperthermia is based on the assumption that it may enhance the effect of the chemotherapy, especially cisplatin-based treatments[6-8]. There are some experimental studies providing evidence that hyperthermia can affect cell membranes, cytoskeletons, synthesis of macromolecules, increase drug-induced DNA damage, and inhibit the repair of drug-induced DNA damage[9]. Hyperthermia may provide higher local cisplatin concentrations in tissues, indicating the pharmacokinetic advantage of its use and reduction of systemic toxicity[10]. Hyperthermia-induced PARP blockade can increase chemotherapy-induced damage in BRCA-competent cells of ovarian and colon cancer[11].

However, the results of available studies on the synergy of hyperthermia and cisplatin chemotoxicity, initiation of apoptosis, and intracellular accumulation of cisplatin in different gastrointestinal cancer cells are controversial. The opposite effect of hyperthermia on cisplatin sensitivity was observed in mismatch repair deficiency and mismatch repair proficiency in colon cancer cell lines[12]. Isolated hyperthermia only temporarily inhibited cell proliferation without cytotoxic effects on gastric cancer cell lines. However, a synergistic effect of hyperthermia and chemotherapy on inhibiting proliferation and induction of cell death via the apoptotic pathway was reported[13]. Interestingly, the hyperthermia-mediated increase of cellular accumulation of cisplatin and persistent DNA damage in gastric cancer cells was observed only with the addition of tumor necrosis factor[14]. The expression of heat shock genes and proteins provides an adaptive mechanism for stress tolerance, allowing cells to survive non-physiologic conditions. However, the same adaptive mechanism can ultimately favor malignant transformation by interfering with pathways that regulate cell growth and apoptosis. Cytoprotection and thermotolerance raised the concern that heat-treated tumor cells might also be resistant to attack by immune effector mechanisms[15]. Data on the additive effect of hyperthermia in terms of enhanced chemo-cytotoxicity in cancer cells of pancreatic origin are scarce.

Therefore, the aim of this study was to analyze the additivity of hyperthermia to cisplatin effects in gastric, pancreatic, and colorectal cancer cell lines evaluating cell cytotoxicity, apoptosis, and intracellular cisplatin concentration.

MATERIALS AND METHODS

Human cancer cell lines

The AGS and Caco-2 cell lines were purchased from American Type Cell Culture (ATCC Manassas, VA, United States). AGS cell line is derived from a gastric adenocarcinoma of the stomach of a 54 year-old Caucasian female with no prior anti-cancer treatment. Caco-2 cells were isolated from a primary colonic tumor in a 72-year-old Caucasian male using the explant culture technique. Forms moderately well differentiated adenocarcinomas consistent with colonic primary grade II, in nude mice. T3M4 cell line was obtained as a gift from the European Pancreas Center (Heidelberg, Germany). This cell line was derived from a lymph node metastasis of the Japanese male patient, diagnosed with pancreatic ductal adenocarcinoma. It is characterized as pancreatic adenocarcinoma producing CEA, K-ras activated, and with slow cell growth. Cells were grown in RPMI medium (Gibco/Invitrogen, Carlsbad, CA, United States) with the addition of 10% fetal bovine serum (Gibco/Invitrogen) and 1% penicillin/streptomycin solution (Gibco/Invitrogen). Flasks with cells were cultured in a humid incubator with a CO2 level of 5% and temperature of 37 °C.

Design of experiment

Cancer cells were cultivated for 24 h in the conditions described above. Afterwards, cells were treated by one of two separate factors: temperature (37 °C, 38 °C, 39 °C, 40 °C, 41 °C, 42 °C, 43 °C, 44 °C, 45 °C) or IC50 dose of cisplatin, which was specifically determined for each cell line. Moreover, the combination of hyperthermia and cisplatin treatment was applied (Figure 1). The duration of treatment was 1 h as it reflected the treatment time under the clinical conditions of HIPEC. Cells were heated in humid incubators at particular temperature regimens. When temperature of the media reached desired level, we started the countdown of one hour exposure. Medium temperature was controlled by the electronic thermometer. Following the treatment, the medium was changed, and cells were cultivated for 48 h under the conditions as previously described. Afterwards, MTT and flow cytometry were performed (see “MTT assay” and “Cell apoptosis”). All experiments were repeated at least three times.

Figure 1.

Figure 1

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Design of experiment.

MTT assay

Cytotoxicity of cisplatin or/and hyperthermia was determined by MTT [3-(4, 5-dimethylthiazol-2-Yl)-2, 5-diphenyltetrazolium bromide] (Gibco/Invitrogen) assay. The plate was incubated for 4 h at 37 °C after 5 mg/mL of the MTT reagent was added to the wells. Then the supernatant was removed, and DMSO (dimethyl sulfoxide) (Carl Roth GmbH, Karlsruhe, Germany) was added to solubilize the resulting formazan crystals. Absorbance measurements were made at 570 nm on the Sunrise spectrophotometer (Tecan GmbH, Grodig, Austria).

Cell apoptosis

The changes in apoptosis were evaluated after treatment of the cells by hyperthermia (43 °C) and the previously determined IC50 of cisplatin (specific for particular cell line). Untreated cisplatin cells and normothermia (37 °C) cultivated cells were defined as controls. Forty-eight hours after the experiment (Figure 1), the rate of apoptosis was determined by flow cytometer Guava Nexin Annexin V Assay (Merck, Millipore United States and Canada). All the procedures were performed according to the manufacturer’s instructions. Samples were measured using a Guava Personal Cell Analysis (PCA) Flow Cytometer (Merck, Millipore) and CytoSoft software.

Intracellular concentration of cisplatin

Immediately after the experiment, the cell lysate samples were diluted ten times with high purity deionized water. Concentration of total intracellular cisplatin was analyzed by inductively coupled plasma mass spectrometer (ICP-MS) NexION™ 300D (PerkinElmer, United States) equipped with nickel cones and a quartz cyclonic spray chamber as a sample introduction system and using collision mode kinetic energy discrimination (KED) with helium gas (purity ≥ 99.999%) to remove polyatomic interferences. The calibration graphs for determination of Platinum by ICP-MS were prepared in the range of 0-50 ng/mL using Pure Plus 10 mg/L Multi-Element calibration standard 4 (PerkinElmer, United States). The working conditions of the spectrometer were optimized daily in order to obtain the maximal sensitivity and stability.

Isobologram analysis

To identify the confidence limits for the additive action of hyperthermia and cisplatin, isobologram analysis was applied. Data for analysis was obtained from the MTT test. Temperature data points of 38 °C, 39 °C, 40 °C, 41 °C, 42 °C, 43 °C, 44 °C, and 45 °C, and cisplatin concentration data points of 25 μmol/L, 50 μmol/L, 100 μmol/L, 200 μmol/L, and 400 μmol/L were used to define the dose effect curve for temperature and cisplatin, respectively. For combined treatment analysis, the following combinations of factors were used: 39 °C + 50 μmol/L; 39 °C + 100 μmol/L; 39 °C + 200 μmol/L; 40 °C + 50 μmol/L; 40 °C + 100 μmol/L; 40 °C + 200 µmol/L; 41 °C + 50 μmol/L; 41 °C + 100 μmol/L; 41 °C + 200 μmol/L; 42 °C + 50 μmol/L; 42 °C + 100 μmol/L; 42 °C + 200 μmol/L; 43 °C + 50 μmol/L; 43 °C + 100 μmol/L; 43 °C + 200 μmol/L; 44 °C + 50 μmol/L; 44 °C + 100 μmol/L; 44 °C + 200 μmol/L. The Chou median effect equation was used[16]. It provides the theoretical basis for the combination index (CI), which enabled quantification of drug interaction affects defining synergism (CI < 1), additivity (CI = 1), or antagonism (CI > 1). The CompuSyn software (CompuSyn, Inc., Paramus, NJ, United States) was used for calculations.

RESULTS

Different cell lines have specific responses to hyperthermia

To evaluate the effect of hyperthermia per se on different cancer cells in vitro, we examined the response of the AGS, Caco-2, and T3M4 cell lines to temperature using a stepwise increase of one degree ranging from 37 °C to 45 °C. Cell viability was determined by MTT assay. Every cell line demonstrated a different pattern of response to hyperthermia (Figure 2). AGS cells were the most sensitive one to hyperthermia, where a temperature rise from 41 °C to 45 °C gradually decreased its viability by 30%. In the 37 °C to 41 °C interval, the viability stayed constant. Cells affected by 43 °C, 44 °C, and 45 °C dropped their viability rate by 16%, 22 °C, and 30%, respectively, as compared to the control (37 °C). A temperature increase from 37 °C to 42 °C had no significant effect on Caco-2 cells, but at 43 °C and 44 °C, its viability dropped by 14% and 20%, respectively, but stayed constant at higher temperatures. The response of T3M4 cells to the changes of temperature was different. Temperatures from 37 °C to 42 °C decreased its viability by 30%. At 43 °C, the viability of T3M4 cells sharply increased by 20% and stayed at this level in higher temperatures. Overall, only the AGS cell line responded to hyperthermia as implied, with gradual inhibition of cell viability.

Figure 2.

Figure 2

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The different effect of the temperature on cancer cell viability. Following a one-hour exposure of AGS, Caco-2, and T3M4 cells to temperatures ranging from 37 °C to 42 °C, there were no significant viability changes. Starting at 43 °C, viability gradually decreased in AGS and Caco-2 cells. Activation of viability was evident in T3M4 cells at temperatures of 43 °C and 44 °C. All data were compared with a control group (viability of cells at temperature of 37 °C set as 100%). Statistical analysis was performed using the Mann-Whitney U test comparing selected groups to the control. aP < 0.05 vs control.

Different cell lines respond to cisplatin in a comparable linear pattern but with specific sensitivity

Cisplatin induced a dose-dependent suppressor effect on cancer cell viability, with a similar linear response in the AGS, Caco-2, and T3M4 cell lines. Pancreatic cancer cells (T3M4) were the most sensitive, revealing cisplatin IC50 at 48 μmol/L. The IC50 for Caco-2 was 194 μmol/L, and for AGS, it was 182 μmol/L (Figure 3).

Figure 3.

Figure 3

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The influence of different cisplatin doses on cancer cell viability. Exposure to gradually increasing doses of cisplatin resulted in a linear decrease of viability in all cancer cell lines. T3M4 cells were the most sensitive to cisplatin, followed by Caco-2 and AGS cells. All data were compared with the control group (viability of cells at 37 °C set as 100%). Data are presented as the mean ± SE from ≥ 3 replicates.

Insufficient temperature regimens can be detrimental in combined hyperthermic chemotherapy

Previously determined IC50 doses of cisplatin were used for particular cell lines during this experiment. Simultaneous exposure of cells to hyperthermic conditions and cisplatin triggered different response in AGS, Caco-2, and T3M4 cells (Figure 4). Overall, temperatures ranging from 37 °C to 41 °C had no detectable additive effect to cisplatin cytotoxicity. Interestingly, we observed peaks of viability in AGS (42 °C, increase by 33%) and T3M4 (43 °C, increase by 32%) cells. Higher temperatures, in addition to cisplatin exposure, inhibited cell growth dramatically; AGS viability dropped by 70% and T3M4 dropped by 76% at 45 °C. Application of hyperthermia in addition to cisplatin in the Caco-2 cell line gradually improved the cytotoxic effect and decreased the viability of cells by one-fourth from 43 °C to 45 °C. In summary, application of hyperthermia (43 °C and higher) in addition to cisplatin might enhance its cytotoxic effect in the Caco-2 cell line. However, lower (e.g., < 43 °C) temperature regimens may even promote cell proliferation and worsen expected hyperthermal chemotherapy effects in AGS and T3M4 cell lines.

Figure 4.

Figure 4

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Effect of temperature and cisplatin (IC50) combinations on cancer cell viability. The increase of temperature had no significant additional effect on cancer cell viability with the exception of extreme hyperthermia (44 °C-45 °C). Peaks of enhanced viability were observed in AGS and T3M4 cells at temperatures of 42 °C and 43 °C. Data are equalized to control (untreated cells) as 100% and shown in percentages. Dashed line shows IC50.

Isobologram analysis: Unpredictable response of the cells to hyperthermia and cisplatin

We constructed isobolograms to reveal if the combined application of hyperthermia and cisplatin had synergistic, antagonistic, or additive effects. Combination of temperature and cisplatin was strongly antagonistic for AGS cells in all studied data points. Combined application of hyperthermia and cisplatin was tripled in Caco-2 cells: synergistic (at 40 °C with 50 μmol/L and 100 μmol/L of cisplatin, at 43 °C with 50 μmol/L, 100 μmol/L, and 200 μmol/L cisplatin, at 44 °C with 50 μmol/L , 100 μmol/L, and 200 μmol/L of cisplatin), additive (at 39 °C with 100 μmol/L of cisplatin, at 41 °C with 100 μmol/L cisplatin, and at 42 °C with 50 μmol/L and 100 μmol/L of cisplatin), and antagonistic (at 39 °C with 200 μmol/L of cisplatin, at 40 °C with 200 μmol/L cisplatin, at 41 °C with 50 μmol/L and 200 μmol/L cisplatin, and at 42 °C with 200 μmol/L of cisplatin). Combined treatment of T3M4 at 41 °C with 200 μmol/L cisplatin, at 42 °C with 50 μmol/L cisplatin, and at 44 °C with 100 μmol/L and 200 μmol/L of cisplatin had an additive effect. The remaining combinations were antagonistic (Figure 5).

Figure 5.

Figure 5

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Interaction of temperature and cisplatin using the isobologram method for cancer cell viability. Mathematically revealed combined effects of hyperthermia and cisplatin differ in AGS, Caco-2, and T3M4 cell lines. The isobologram represents the interaction between cisplatin and temperature resulting in inhibition of cancer cell growth. The solid line in the diagram (Combination Index = 1) indicates the alignment of theoretical values of an additive interaction between two effectors and represents calculated conditions required to inhibit cell growth by 50%. Mathematically calculated IC50 for AGS cells: temperature 51 °C, cisplatin 159 μmol/L; Caco-2 cells: temperature 66 °C, cisplatin 328 μmol/L; T3M4 cells: temperature 61 °C, cisplatin 0 μmol/L. Treatment combination points falling above the line indicate mathematical antagonism (below synergism, on the line additivity). Combination points that are distant from the line are not shown. Tables on the right represent the CI of selected combinations.

Hyperthermia addition to cisplatin enhances rates of early apoptosis

Annexin V-PE flow cytometry analysis was performed to evaluate rates of early apoptosis. Cisplatin induced early apoptosis in Caco-2 and T3M4 cells 1.5-fold and 3.4-fold, respectively. The number of dead/late apoptotic cells was insignificant in the following groups: 0.5% of Caco-2 cells and 2.9% of T3M4 cells. Hyperthermia of 43 °C in addition to cisplatin induced early apoptosis as compared to cells treated in normothermia by 20% in Caco-2 (1% of dead cells) and 19% (3.9% dead cells) in T3M4, respectively. Interestingly, early apoptosis was not significantly induced by isolated cisplatin treatment in AGS cells. Rates of AGS early apoptosis were not significantly induced by an isolated cisplatin treatment. However, application of combined treatment with hyperthermia and cisplatin increased early apoptosis by 61% (0.4% dead cells) (Figure 6).

Figure 6.

Figure 6

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Apoptotic effect of temperature and cisplatin in cancer cells. A: Early apoptosis was significantly induced by hyperthermia in cisplatin-treated cells, with the exception of Caco-2 cells, where temperature had no significant role. The dashed line represents control rates of apoptosis in untreated cells. Statistical analysis was performed using the Mann-Whitney U test. aP < 0.05. B: Dot plots presenting change of apoptosis in cisplatin untreated/treated cells and cultivated in hyperthermia. “-cis”: Cisplatin untreated cells; “+cis”: Cisplatin treated cells.

Hyperthermia increases intracellular cisplatin concentration

Hypothesizing that hyperthermia promotes delivery of cisplatin to cancer cells, we aimed to measure intracellular cisplatin concentrations. Analysis was performed immediately following a one-hour exposure to the IC50 of cisplatin at 37 °C and 43 °C. Overall, 43 °C promoted an increase of intracellular cisplatin concentration. The concentration was significantly increased in AGS, Caco-2, and T3M4 cells by 30%, 20%, and 18%, respectively (Figure 7).

Figure 7.

Figure 7

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The change of the intracellular cisplatin concentration. Temperature of 43 °C significantly increased the intracellular concentration of cisplatin in all analyzed cell lines. Data are shown as concentrations of ng/mL. Statistical analysis was performed using the Mann-Whitney U test. aP < 0.05. “+cis”: Cisplatin treated cells.

DISCUSSION

Hyperthermal intraperitoneal chemotherapy has been applied to treat peritoneal carcinomatosis for gastric[17-19], colorectal[20], ovarian[21], and peritoneal mesothelioma[22] and has aided in prolonged long-term survival in selected patients[23-26]. In HIPEC, intraperitoneal free cancer cells and the serous surface of the bowel and peritoneum are exposed to high concentrations of chemotherapy agents. Hyperthermia itself may affect cell cytoskeletons, cell membranes, synthesis of macromolecules, and DNA repair mechanisms[9].

As the origin, genotypes, and phenotypes of free cancer cells may be quite different, it seems unreasonable to treat all peritoneal metastases the same way. Until now, basic information regarding the contribution of hyperthermia to intraperitoneal chemotherapeutic agents in different gastrointestinal cancers is poor and controversial. In this in vitro study, we have applied hyperthermia and chemotherapy for 1 h in order to mimic clinical conditions. We have performed our aimed readouts at 48 h following the experiment as the earlier readouts have not proven any changes.

We have chosen three most common peritoneum invading GI cancers in our study, selecting one cancer cell line per cancer type. It is known that various cancer cells of same cancer type are different in the manner of apoptosis, biomarker expression etc [27]. This study is an overview, which leads to a better knowledge of gastric, pancreatic and colorectal cancer cell response to simultaneous hyperthermia and cisplatin treatment.

Until now, our analyzed cells are well examined in various aspects. AGS cells in 516 analyzed genes, have 40 mutations, like KRAS, WNK1 and WNK2[28]. Overexpression of HER-2, EGFR, VEGF, Bcl-2 biomarkers was investigated in gastric cancer cells[29]. Mutations of SMAD4 and TP53 genes and overexpression of ILF3, TIMP3 genes are present in Caco-2 cells[30-32] . T3M4 are the least examined cells. No known gene mutations were found[33] and they are known to overexpress growth factors as FGFR4[34].

Our experiments revealed the differences of cell viability in response to isolated hyperthermia. We even observed positive effects of isolated hyperthermia on the viability of pancreatic cancer cells. We hypothesize that this effect could be related to the activation of the cytoprotective heat shock proteins (HSP), an effect described in other studies[35]. It is known that higher temperatures can enhance thermotolerance by activating HSPs[36]. However, gastric cancer cells (AGS) and colon cancer cells (Caco-2) responded to hyperthermia with a significant drop of viability at 43 °C. One study demonstrated that hyperthermia alone can significantly reduce viability of the Colon 26 cancer cells[37]. The investigation of the effect of local heat used for ablation of tumor nodules showed that exposing cultured Caco-2 cells to 48 °C for 2 h resulted in an approximately 80% reduction of cell viability[38]. However, in our study, the viability of Caco-2 cells decreased only by 14% after exposure to 43 °C for 1 h.

Hyperthermia may enhance the effect of chemotherapy, especially cisplatin-based treatments[6-8]. Ferraro et al[39] studied the effects of hyperthermia and cisplatin on model protein hen eggs and revealed that increased temperature enhanced cisplatin cytotoxicity.

Tang et al[13] have shown a synergistic effect of hyperthermia and chemotherapy inhibiting proliferation in six gastric cancer cell lines, including AGS, in a certain range of chemoagent (cisplatin) concentration. Moreover, hyperthermia, in addition to chemotherapy, induced cell apoptosis as the major type of death. MicroRNA-218 upregulation and increased chemosensitivity were observed in gastric cancer cells after exposing them to hyperthermal conditions[40]. However, in our study, only temperatures higher than 43 °C in addition to cisplatin exposure inhibited cell growth. In the isobologram analysis, the combination of temperature and cisplatin was antagonistic for AGS cells. On the contrary, AGS cells showed an increased viability of 33% at 42 °C. This is an important observation as it may highlight the possibility that technically incorrect temperature regimens may activate metabolism of cancer cells and increase their resistance to chemotherapy. Interestingly, we observed that application of cisplatin to gastric cancer (AGS) cells for one h had no significant impact on cell apoptosis. However, the combination of cisplatin and hyperthermia (43 °C) increased the affect by 61%. Our results suggest that temperature and cisplatin are not always acting in synergy as was shown by isobolograms.

Previous in vitro investigations have revealed that the response of the colon cancer cells to hyperthermia and chemotherapeutic drug differ by cell type. Some authors have shown that hyperthermia alone significantly decreased the viability of the Colon 26 cancer cells[37], and the cytotoxic effect of cisplatin[41] was enhanced at hyperthermal conditions. After exposure to 43 °C, the activity of oxaliplatin markedly and rapidly increased, indicating its inhibiting potential in Colon 26 cells[42]. Significant synergy of hyperthermia and chemotherapy was detected in CX-1 cells[43] in similar experimental conditions (42 °C for 1 h). Some authors described similar results in HCT116+ch2 (MMR-) cells that were resistant to heat treatment at temperatures of 41 °C and 42 °C[12]. The exposition of the colon carcinoma cell lines CX-1 and HTC 116 to 42 °C for 1 h revealed no change in cell viability[13,43]. Moreover, HCT116+ch2 (MMR-) cells exposed to a mild heat were 1.42-fold more resistant to cisplatin[12]. We observed that the addition of hyperthermia to cisplatin treatment had a slight positive influence on Caco-2 cell viability. At 43 °C, cisplatin had an insignificant effect regarding apoptosis, whereas intracellular cisplatin concentration was elevated by 26% as compared to the control. Isobologram analysis showed approximately 50% of selected cisplatin and temperature treatment combinations acted in a synergistic manner, indicating that some of hyperthermic chemotherapy regimens might be useful.

Recent studies reported that hyperthermia increased sensitivity to gemcitabine[44] and enhanced gemcitabine-related apoptotic cell death in pancreatic cancer cells[45]. Moreover, the improved drug delivery and antitumor effects in combination with mild hyperthermia were reported [46].

The combined cytotoxic effect of cisplatin and hyperthermia in T3M4 cells was evident only when the temperature was higher than 43 °C. These cells were the most sensitive to cisplatin with the lowest IC50. Cisplatin amplified apoptosis by 3.4-fold and hyperthermia increased the effect by 19%; however, it was 3-fold less in the gastric cancer cell line. Similar to AGS cells, T3M4 isobologram analysis revealed that the combination of treatments acted in an antagonistic manner in most of the selected combinations; however, in few of them, the additive effect of the two agents was revealed. An extremely limited increase of intracellular cisplatin concentration in hyperthermia could be observed in pancreatic cancer cells. Our experiments elucidated that the response of T3M4 cells differs from other studied gastrointestinal cancer cells (AGS and Caco-2). A review by Loggie et al[47] postulated that hyperthermia combined with chemotherapy is probably beneficial for less aggressive tumors and should be the standard of care for appendiceal and colorectal cancers.

Caco-2 cell results varied from the other cells in our study. In some cases, they acted in unpredictable manner. One of the possible explanations for this discrepancy, would be that Caco-2 cells can differentiate their phenotype prior to post-confluence stage, and lead to the change of morphology, degree of differentiation etc[48].

In summary, we have proven that the role of hyperthermia in addition to cisplatin is different in gastric, colonic, and pancreatic cancer cells. The overview of the basic results is shown in Table 1. Different cancer cells respond to combined treatments in different manners, and temperature-induced apoptosis is initiated by various pathways[49].

Table 1.

Overview of results

Cell line Effect of temperature at 43 °C on cancer cells viability IC50 dose of cisplatin Combined effect of temperature, at 43 °C and IC50 dose of cisplatin on cancer cells viability Effect of temperature in addition to IC50 dose of cisplatin on cancer cell apoptosis Effect of temperature on intracellular cisplatin concentration
AGS ↓↓ 182 ↓ ↑ ↑↑↑
Caco-2 ↓ 194 ↓↓ - ↑↑
T3M4 - 48 - ↑ ↑
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The number of the arrows represents strength of effect.

In conclusion, hyperthermia up to 43 °C in addition to cisplatin does not influence AGS, Caco-2, and T3M4 cell viability in a synergistic manner. However, some regimens of hyperthermia and cisplatin treatment are beneficial regarding the apoptotic response and an increase of intracellular cisplatin concentration.

ARTICLE HIGHLIGHTS

Research background

Hyperthermal intraperitoneal chemotherapy is an option to treat peritoneum invading gastrointestinal cancer. Until now the results of hyperthermal intraperitoneal chemotherapy (HIPEC) treatment are controversy, needing unification in selected parameters of the treatment. In different cancer centers, the procedure varies in time setting, hyperthermia level and different chemotherapy drugs are used.

Research motivation

As HIPEC is widely used in clinical practice, still there is a lack of studies, analyzing the impact of hyperthermia and cisplatin to cancer cells. The cellular response to the treatment is still not clear. There is no clear data defining optimal timing and temperature of the procedure.

Research objectives

Our objective was to analyze gastric, pancreatic and colorectal cancer cells response to hyperthermia and cisplatin treatment regarding viability, change of intracellular cisplatin concentration and apoptosis rate.

Research methods

We used AGS (gastric cancer), T3M4 (pancreatic cancer) and Caco-2 (colorectal cancer) cells. Mimicking HIPEC procedure, cells were treated with specific to each cell line IC50 dose of cisplatin at the temperature regimens ranging from 37 °C to 45 °C. Treatment lasted for one hour. Later cells were harvested in normothermia, changing cisplatin containing media to fresh one. Immediately after experiment, intracellular cisplatin concentration was measured, using mass spectrometer analysis. For other readouts cells were harvested for 48 hours in normal conditions. MTT test was performed for cellular viability evaluation and isobologram analysis. We used flow cytometry to determine apoptosis change of hyperthermia and cisplatin treatment.

Research results

Cells responded to hyperthermia (ranging from 38 °C to 45 °C) in a different manner. Viability of AGS cells was the most hyperthermia-dependent, decreasing by 30% (from 41 °C to 45 °C). Caco-2 cell viability had no change in the interval from 38 °C to 42 °C. Higher temperature regimens dropped its viability rate by 14%-20%. T3M4 cells reacted differently. Viability dropped until 42 °C, but at higher temperature regimens, we observed increase of viability. While in simultaneous hyperthermia and cisplatin treatment, we observed no change of viability until 41 °C in all cancer cells. Higher temperatures inhibited cell growth. Interestingly, we observed peaks of viability in AGS (42 °C, increase by 33%) and T3M4 (43 °C, increase by 32%) cells. Putting all MTT data to isobologram analysis, we observed synergistic, antagonistic, or additive effects of combined treatment. Hyperthermia and cisplatin treatment was strongly antagonistic in AGS cells. In Caco-2 cells we observed synergistic, additive and antagonistic effects of simultaneous treatment. Few combined treatment regimens were additive for T3M4 cells, and remaining antagonistic. Cisplatin induced early apoptosis in Caco-2 and T3M4 cells 1.5-fold and 3.4-fold, respectively. Hyperthermia of 43 °C in addition to cisplatin induced early apoptosis as compared to cells treated in normothermia by 20% in Caco-2 and 19% in T3M4, respectively. Hyperthermia strongly decreased intracellular cisplatin concentration in AGS, Caco-2, and T3M4 cells by 30%, 20%, and 18%, respectively.

Research conclusions

Our data suggest that HIPEC conditions have to be cancer type dependent and well revised. Particular temperature regimens can do more harm, than benefit, by activating cell division and growth.

Research perspectives

To get better knowledge of hyperthermia and cisplatin treatment effects, future studies should include more cancer cell lines per cancer type. Also, in vivo vehicle should be established.

Footnotes

Manuscript source: Unsolicited manuscript

Specialty type: Gastroenterology and hepatology

Country of origin: Lithuania

Peer-review report classification

Grade A (Excellent): 0

Grade B (Very good): B

Grade C (Good): C

Grade D (Fair): 0

Grade E (Poor): 0

Supported by the Research Council of Lithuania, No. SEN-01/2015.

Institutional review board statement: The study was reviewed and approved by the Kaunas Regional Biomedical Research Ethics Committee.

Conflict-of-interest statement: All authors have nothing to disclose.

Data sharing statement: No additional data are available.

Peer-review started: December 2, 2017

First decision: December 27, 2017

Article in press: January 16, 2018

P- Reviewer: Caboclo JL, Zhu YL S- Editor:Gong ZM L- Editor: A E- Editor: Ma YJ

Contributor Information

Vaidotas Cesna, Department of Surgery, Lithuanian University of Health Sciences, Kaunas LT-50161, Lithuania.

Arturas Sukovas, Department of Obstetrics and Gynecology, Lithuanian University of Health Sciences, Kaunas LT-50161, Lithuania.

Aldona Jasukaitiene, Institute for Digestive Research, Lithuanian University of Health Sciences, Kaunas LT-50161, Lithuania.

Rima Naginiene, Neuroscience Institute, Lithuanian University of Health Sciences, Kaunas LT-50161, Lithuania.

Giedrius Barauskas, Department of Surgery, Lithuanian University of Health Sciences, Kaunas LT-50161, Lithuania.

Zilvinas Dambrauskas, Institute for Digestive Research, Lithuanian University of Health Sciences, Kaunas LT-50161, Lithuania. zilvinas.dambrauskas@lsmuni.lt.

Saulius Paskauskas, Department of Obstetrics and Gynecology, Lithuanian University of Health Sciences, Kaunas LT-50161, Lithuania.

Antanas Gulbinas, Institute for Digestive Research, Lithuanian University of Health Sciences, Kaunas LT-50161, Lithuania.

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