Background
In China, gastric cancer (GC) is the second leading cause of cancer-related deaths, and about 80% of patients with GC are diagnosed at an advanced stage [
1,
2]. Typically, chemotherapy is the cornerstone of treatment for advanced gastric cancer (AGC). Despite the fact that the combination of fluorouracil-based chemotherapy and trastuzumab has provided HER2-positive patients with significant survival benefit [
3], prognosis for patients with AGC is still grave due to the limited treatment options and inevitable drug resistance. Therefore, exploring potential novel drugs is needed for GC.
Camptothecin (CPT) is a pentacyclic quinoline alkaloid isolated from the Chinese
Camptotheca acuminata tree. Based on the CPT structure, 10-hydroxycamptothecin (HCPT), irinotecan, topotecan, gimatecan and other analogues have been developed as broad-spectrum antitumor drugs to treat colorectal cancer [
4], lung cancer [
5], melanoma [
6], hepatic carcinoma [
7] and neuroblastoma [
8]. The direct target of CPT and its derivatives is DNA topoisomerase I (TopI), which breaks DNA by bonding to 3′-phosphates [
9]. TopI is susceptible to inhibitors when DNA is in a cleaved state, allowing inhibitors to convert transient TopI-DNA complexes to permanently damaged strands. These inhibitors have weak affinities for the enzyme or DNA alone [
10]. In addition to negative regulation of TopI, HCPT has been reported to enhance apoptosis via p53 [
8], p38 MAPK, ERK, AKT [
11], and NF-κB [
12] pathways.
Gimatecan, which is an orally bioavailable CPT analogues and has greater and more persistent DNA cleavage than other CPTs [
13‐
15], has been shown to have strong preclinical antitumor activity against a panel of human tumor xenografts [
16‐
20]. Furthermore, a phase I study in 33 patients with advanced solid tumors confirmed the antitumor activity and acceptable tolerability of gimatecan, which warrants further clinical researches to evaluate the efficacy of gimatecan monotherapy or combination with other agents [
21‐
24]. Irinotecan is frequently used in GC patients as second- or third-line therapy, but whether gimatecan has antitumor activity against GC is unclear.
Methods
Cell lines
Human GC cell lines SNU-1, HGC27 and MGC803 were purchased from Peking Union Medical College, and the NCI-N87 cell line was a gift from You-yong Lv, Ph.D. (Peking University Cancer Hospital and Institute). Cells were cultured in RPMI 1640 medium and Dulbecco’s Modified Eagle Medium (Gibco-BRL, MD, USA), respectively, supplemented with 10% fetal bovine serum (Gibco-BRL), 100 U/ml penicillin (Gibco-BRL) and 100 mg/ml streptomycin (Gibco-BRL). Cells were incubated in a humidified incubator (37 °C) supplemented with 5% CO2.
Inhibitors and antibodies
Gimatecan (purity ≥ 99.9%) was provided by Zhaoke Pharmaceutical Ltd. (Hefei, China), and irinotecan hydrochloride (purity = 99.91%) was purchased from Jiangsu Hengrui Medicine Co., Ltd. (Jiangsu, China). Gimatecan was dissolved in DMSO at a stock concentration of 10 mmol/l and 12.5 mg/ml for in vitro and in vivo studies, respectively, and then stored at − 80 °C for future use. Irinotecan was diluted in 0.9% NaCl at a concentration of 10 mmol/l and 20 mg/ml immediately before use. AKT, pAKT, S6, pS6, ERK, pERK, MEK, pMEK, p38 MAPK, p-p38 MAPK, JNK2, pJNK2, Bcl-2, Bak, PARP, cleaved PARP, MDR1, ABCG2 and DNA Topoisomerase I antibodies were purchased from Cell Signaling Technology (Boston, MA, USA). β-Actin antibody was purchased from Sigma-Aldrich (St. Louis, Missouri).
Cell viability assay
SNU-1, HGC27, MGC803 and NCI-N87 cells (5000 cells/well) were seeded in 96-well plates and incubated overnight in complete medium, followed by exposure to gimatecan (0–1 µM) or irinotecan (0–1 µM) for 24, 48, or 72 h. Cell viability was measured using a Cell Counting Kit-8 (Dojindo, Kumamoto, Japan) according to the manufacturer’s instructions. Absorbance at 450 nm was measured using a microplate spectrophotometer. All experiments were repeated at least three times.
Annexin V apoptosis assay
Apoptosis was measured by staining with phycoerythrin (PE)-annexin V and 7-amino-actinomycin (7-AAD) (BD Biosciences, Erembodegem, Belgium) for 15 min at room temperature in the dark, followed by flow cytometry (BD Biosciences) within 1 h. Apoptosis was analyzed with FlowJo 7.6 software (FlowJo, LLC, Ashland, Oregon).
Animal experiments
Establishment and serial passaging of GC patient-derived xenografts (PDX) models were as previously described [
25]. All procedures were performed under sterile conditions at an SPF facility and carried out in accordance with the guide for the Care and Use of Laboratory Animals of the National Institutes of Health. Animal experiments were approved by an independent ethics committee of Peking University Cancer Hospital.
Five PDX tissues were subcutaneously inoculated into the flanks of 6-week-old female non-obese diabetic/severe combined immunodeficiency (NOD/SCID) mice. When tumors reached 150–250 mm3, mice were randomized to three groups (N = 5/group) with similar tumor volumes: (1) control group (physiological saline 100 µl daily, by orally gavage), (2) gimatecan group (gimatecan 0.2 mg/kg daily, by orally gavage) and (3) irinotecan group (irinotecan 20 mg/kg via weekly intraperitoneal injection). All animals were treated for 3 weeks. Tumor size and body weight were measured twice a week, and tumor volume was calculated using the following formula: V = (L × W2)/2 (V, volume; L, length; W, width). Tumor growth inhibition (TGI) was calculated using the following formula: TGI = 1 − ΔT/ΔC × 100% (ΔT = tumor volume changes of the drug treated group, ΔC = tumor volume changes of the control group on the final day of the study).
Western blot
SNU-1, HGC27 and NCI-N87 cells were starved in serum-free medium overnight, exposed to inhibitors for 48 h and harvested at 70–80% confluence. Total protein was extracted from cells or xenograft tissues on ice, using RIPA Lysis Buffer (Beyotime, Shanghai, China) supplemented with complete protease inhibitor and phosphatase inhibitor cocktail (Roche, Basel, Switzerland). Protein concentration was measured using a BCA Protein Assay Kit (Beyotime, Shanghai, China), and 50 μg protein from each sample was separated by 10% SDS-PAGE. After transfer to nitrocellulose membranes (GE Healthcare, Piscataway, NJ), samples were incubated with corresponding primary antibodies diluted in 5% BSA at 4 °C overnight and then with secondary antibodies at room temperature for 1 h. Proteins were visualized with a chemiluminescent detection system (GE Healthcare), using ECL plus Western blot reagents (GE Healthcare). Western-blotting bands were quantified and normalized by ImageJ software.
Immunohistochemistry (IHC) staining of Ki-67
After mice were sacrificed, xenograft tissues were isolated, and formalin-fixed paraffin embedded (FFPE) tissue sections were prepared. After deparaffinization, hydration, endogenous peroxidase treatment, and retrieval, 4-μm-thick FFPE sections were incubated with primary antibodies (1:100) overnight at 4 °C. The signal was assayed after incubation with IgG-HRP polymer (ZSGB-BIO, Beijing, China) and diaminobenzidine substrate. Sections were interpreted by pathologists from the Department of Pathology of Peking University Cancer Hospital who were blinded to this study. The scoring standard of Ki-67 was consistent with a previous report [
26].
Statistical analysis
Statistical analysis was performed with Graphpad Prism version 6.0 (Graphpad software). For in vitro studies, differences between the groups were analyzed using an unpaired two-tailed t test. For in vivo studies, tumor growth among different groups was compared using repeated measures ANOVA and p < 0.05 was considered statistically significant.
Discussion
In this study, we evaluated the efficacy and underlying mechanism of gimatecan and irinotecan in vitro and in vivo. Gimatecan had significant antitumor activity as indicated by inhibition of cell proliferation, suppression of xenograft growth, and activation of apoptosis.
As is known to us, TopIs have been described as molecular targets for CPT and its derivatives, and TopI is essential for DNA replication, recombination, and damage repair. Two water-soluble CPT derivatives have been approved by the FDA: topotecan for ovarian cancer and recurrent small cell lung cancer [
10], and irinotecan for gastrointestinal cancer, which has been developed as a single agent or in combination with other cytotoxic agents for second- or third-line therapy for advanced AGC [
27‐
30]. However, the instability of lactone ring and poor oral bioavailability have been reported to be major limitations of water-soluble CPT derivatives in clinical practice [
31].
As the third orally bioavailable CPT analogue, gimatecan induced proliferative inhibition and apoptosis promotion in GC cells at a lower concentration, which was consistent with previous studies [
13‐
18]. In 2007, Marchetti et al. reported that the ABCG2 expression resulted in eight to tenfold resistance to gimatecan, which could be reversed by the ABCG2 or MDR1 inhibitors [
32]. In this study, we detected the expression of ABCG2 and MDR1 in four GC cell lines and observed higher expression of ABCG2 and MDR1 in NCI-N87 cell line, which might be the reason why gimatecan was relatively insensitive to NCI-N87 cells. Moreover, it was well known that most chemotherapeutics had effect on normal cells, therefore, our result also suggested that gimatecan could lead to weak growth inhibition in normal immortalized gastric epithelial cell line (data not shown). But even so, the inhibitory activity of gimatecan was still a promising strategy in the treatment of AGC.
Gimatecan has been reported to decrease expression and activity of TopI, and induce cell cycle arrest at the S phase via cytotoxicity [
17]. Other potential molecular events such as upregulation of TRAIL-R1 and -R2 [
33], inhibition of pAkt and induction of anti-angiogenesis [
20] have been reported and efforts have been made to explore TopI mutations [
15] and plasma alpha1-acid glycoprotein as biomarkers [
34]. In the present study, we tried to elaborate the potential mechanism of mitochondria-dependent apoptosis induced by MAPK pathways.
As critical regulators of cell apoptosis, Bcl-2 family can be divided into pro-apoptotic protein such as Bak, Bad and Bid, and anti-apoptosis proteins including Bcl-2 and Bcl-xl. In our study, compared with irinotecan, gimatecan could induce obvious cell apoptosis accompanied by increased expression of Bak and decreased expression of Bcl-2 in SNU-1 and HGC27 cells. However, cell apoptosis was not significantly observed in xenograft tissues after gimatecan treatment, which might be mainly due to the tumor heterogeneity of xenografts.
Several studies suggest that mitogen-activated protein kinase (MAPK) and Akt signaling pathways respond to extra-cellular stimuli and are involved in apoptosis induced by CPT derivatives [
11,
35]. In brief, the MAPK pathway consists of extracellular-signal-regulated kinase (ERK) which is associated with cell proliferation and growth, and the c-jun N-terminal kinase (JNK) and p38 MAPK pathways which are induced by cellular stress and are closely associated with cell death [
36]. In this study, gimatecan can suppress phosphorylation of Akt and ERK, and increase expression of pJNK2 and p-p38 MAPK at a relatively low concentration in GC cells and PDXs. Inhibition of Akt and ERK signaling was consistent with antitumor activity of gimatecan in cells and in vivo xenografts. Meanwhile, activation of pJNK2 and p-p38 MAPK signaling confirmed cell death induced by a mitochondrial-dependent apoptosis pathway. However, we also found the activation of pJNK2 and p-p38 was inconsistent between SNU-1, HGC27 and NCI-N87 cells. This may partially result from the higher sensitivity of SNU-1 and HGC27 for gimatecan than NCI-N87. Besides, p38 and JNK2 were highly phosphorylated even under no treatment in NCI-N87 cells, which might be difficult to be further upregulated even under the treatment of gimatecan. This phenomenon also suggested the individual difference after the same treatment. Based on present results, we also proposed the hypothesis that p-p38 and pJNK2 levels might be predictive markers for gimatecan, which needed to be further investigated.
Our results indicated that gimatecan exerted significant antitumor activity in GC via suppressing AKT and ERK pathway and activating JNK2 and p38 MAPK pathway. Moreover, gimatecan is an orally bioavailable CPT analogue, whereas irinotecan is an intravenous formulation, suggesting that gimatecan might be an alternative to irinotecan and provided insight of gimatecan in the treatment of GC, which remained to be validated in further clinical research.
Authors’ contributions
LS and JG conceived and designed the study. ZC and ZLiu performed the experiments. WH, ZLi and JZ analyzed the data. JW, XL, BL, DC, YH and JJ contributed reagents, materials, and analysis tools. ZC and JG wrote the manuscript. All authors read and approved the final manuscript.