Kawaguchi Hiroshi, Terai Yoshito, Tanabe Akiko, Sasaki Hiroshi, Takai Masaaki, Fujiwara Satoe, Ashihara Keisuke, Tanaka Yoshimichi, Tanaka Tomohito, Tsunetoh Satoshi, Kanemura Masanori, Ohmichi Masahide
J Ovarian Res. 2014 Apr 9;7:38. doi: 10.1186/1757-2215-7-38.
Gemcitabine (2', 2' -difluorodeoxycytidine) is one of many nonplatinum drugs that exhibit activity in recurrent, platinum-resistant ovarian cancer. However, the molecular mechanisms by which Gemcitabine treatment inhibits the proliferation of platinum-resistant ovarian cancer cells still remain unclear. We investigated whether Gemcitabine increases the efficacy of Cisplatin in platinum-resistant ovarian cancer models in vitro and in vivo.
We used Cisplatin-resistant Caov-3 cells, A2780CP cells and Cisplatin-sensitive A2780 cells to examine the sensitivity of the cell viability of Cisplatin and Gemcitabine using a 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assay and the sensitivity of the invasive activity of Cisplatin and Gemcitabine using an invasion assay with Matrigel. We examined the Akt kinase activity and matrix metalloproteinase 9 (MMP9) expression following Cisplatin and Gemcitabine treatment using a Western blot analysis and the mRNA expression of vascular endothelial growth factor (VEGF) using semi-quantitative RT-PCR. Moreover, we evaluated the effects of Cisplatin and Gemcitabine on the intra-abdominal dissemination of ovarian cancer in vivo.
Gemcitabine significantly inhibited Cisplatin-induced Akt activation in the Caov-3 and A2780CP cells, but not in the A2780 cells. In the presence of Gemcitabine, Cisplatin-induced growth inhibition and apoptosis were significantly enhanced in the Caov-3 and A2780CP cells. Co-treatment with Cisplatin and Gemcitabine almost completely inhibited invasion of both types of cells through the Matrigel; however, neither Cisplatin nor Gemcitabine alone inhibited the invasion of both types of cells. Gemcitabine inhibited not only the Cisplatin-induced activation of Akt, but also the MMP9 and mRNA expression of VEGF. Moreover, treatment with Gemcitabine increased the efficacy of Cisplatin-induced growth inhibition of the intra-abdominal dissemination and production of ascites in the athymic nude mice inoculated with Caov-3 cells.
We herein demonstrated that Gemcitabine inhibits the Akt kinase activity and angiogenetic activity following treatment with Cisplatin in platinum-resistant ovarian cancer cells. These results provide a rationale for using Gemcitabine in clinical regimens containing molecular targeting agents against platinum-resistant ovarian cancers.
吉西他滨(2',2'-二氟脱氧胞苷)是多种对复发性铂耐药卵巢癌具有活性的非铂类药物之一。然而,吉西他滨治疗抑制铂耐药卵巢癌细胞增殖的分子机制仍不清楚。我们研究了吉西他滨是否能在体外和体内铂耐药卵巢癌模型中提高顺铂的疗效。
我们使用耐顺铂的Caov-3细胞、A2780CP细胞和顺铂敏感的A2780细胞,通过3-(4,5-二甲基噻唑-2-基)-5-(3-羧甲氧基苯基)-2-(4-磺基苯基)-2H-四唑(MTS)试验检测顺铂和吉西他滨对细胞活力的敏感性,通过基质胶侵袭试验检测顺铂和吉西他滨对侵袭活性的敏感性。我们使用蛋白质免疫印迹分析检测顺铂和吉西他滨处理后Akt激酶活性和基质金属蛋白酶9(MMP9)表达,使用半定量逆转录聚合酶链反应检测血管内皮生长因子(VEGF)的mRNA表达。此外,我们评估了顺铂和吉西他滨对体内卵巢癌腹腔播散的影响。
吉西他滨显著抑制Caov-3和A2780CP细胞中顺铂诱导的Akt激活,但对A2780细胞无此作用。在吉西他滨存在的情况下,顺铂诱导的Caov-3和A2780CP细胞生长抑制和凋亡显著增强。顺铂和吉西他滨联合处理几乎完全抑制了两种细胞通过基质胶的侵袭;然而,单独使用顺铂或吉西他滨均不能抑制两种细胞的侵袭。吉西他滨不仅抑制顺铂诱导的Akt激活,还抑制MMP9和VEGF的mRNA表达。此外,用吉西他滨治疗可提高顺铂诱导的对接种Caov-3细胞的无胸腺裸鼠腹腔播散和腹水产生的生长抑制疗效。
我们在此证明,在铂耐药卵巢癌细胞中,吉西他滨在顺铂处理后抑制Akt激酶活性和血管生成活性。这些结果为在含分子靶向药物的临床方案中使用吉西他滨治疗铂耐药卵巢癌提供了理论依据。