Morgan Meredith A, Parsels Leslie A, Kollar Laura E, Normolle Daniel P, Maybaum Jonathan, Lawrence Theodore S
Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan 48109-5637, USA.
Clin Cancer Res. 2008 Aug 15;14(16):5142-9. doi: 10.1158/1078-0432.CCR-07-4072.
Gemcitabine-radiotherapy is a standard treatment for locally advanced pancreatic cancer. Clinical data have shown that gemcitabine plus erlotinib is superior to gemcitabine alone for advanced pancreatic cancer. Therefore, we investigated the effects of the combination of epidermal growth factor receptor inhibitors with gemcitabine and radiation on a pancreatic cancer model.
EGFR signaling was analyzed by measuring phosphorylated EGFR (pEGFR(Y845, (Y1173)) and AKT (pAKT(S473)) protein levels in pancreatic cancer cell lines and tumors. The effects of scheduling on gemcitabine-mediated cytotoxicity and radiosensitization combined with erlotinib were determined by clonogenic survival. In vivo, the effects of cetuximab or erlotinib in combination with gemcitabine-radiation on the growth of BxPC-3 tumor xenografts were measured.
We found in vitro that gemcitabine induced phosphorylation of EGFR at Y845 and Y1173 that was blocked by erlotinib. Treatment of BxPC-3 cells with gemcitabine before erlotinib enhanced gemcitabine-mediated cytotoxicity without abrogating radiosensitization. In vivo, cetuximab or erlotinib in combination with gemcitabine-radiation inhibited growth compared with gemcitabine-radiation (time to tumor doubling: gemcitabine + radiation, 19 +/- 3 days; cetuximab + gemcitabine + radiation, 30 +/- 3 days; P < 0.05, erlotinib + gemcitabine + radiation 28 +/- 3 days; P < 0.1). Cetuximab or erlotinib in combination with gemcitabine-radiation resulted in significant inhibition of pEGFR(Y1173) and pAKT(S473) early in treatment, and pEGFR(Y845), pEGFR(Y1173), and pAKT(S473) by the end of treatment. This study shows a novel difference pEGFR(Y845) and pEGFR(Y1173) in response to EGFR inhibition.
These results show that the EGFR inhibitors cetuximab and erlotinib increase the efficacy of gemcitabine-radiation. This work supports the integration of EGFR inhibitors with gemcitabine-radiation in clinical trials for pancreatic cancer.
吉西他滨联合放疗是局部晚期胰腺癌的标准治疗方法。临床数据表明,吉西他滨联合厄洛替尼治疗晚期胰腺癌优于单用吉西他滨。因此,我们研究了表皮生长因子受体抑制剂与吉西他滨及放疗联合应用对胰腺癌模型的影响。
通过检测胰腺癌细胞系和肿瘤中磷酸化表皮生长因子受体(pEGFR(Y845, (Y1173)))和蛋白激酶B(pAKT(S473))的蛋白水平来分析表皮生长因子受体信号通路。通过克隆形成存活率来确定给药方案对吉西他滨介导的细胞毒性和与厄洛替尼联合应用时的放射增敏作用的影响。在体内,检测西妥昔单抗或厄洛替尼联合吉西他滨放疗对BxPC-3肿瘤异种移植物生长的影响。
我们在体外发现,吉西他滨可诱导表皮生长因子受体在Y845和Y1173位点磷酸化,而这一过程可被厄洛替尼阻断。在厄洛替尼之前用吉西他滨处理BxPC-3细胞可增强吉西他滨介导的细胞毒性,且不消除放射增敏作用。在体内,与吉西他滨放疗相比,西妥昔单抗或厄洛替尼联合吉西他滨放疗可抑制肿瘤生长(肿瘤倍增时间:吉西他滨+放疗,19±3天;西妥昔单抗+吉西他滨+放疗,30±3天;P<0.05,厄洛替尼+吉西他滨+放疗,28±3天;P<0.1)。西妥昔单抗或厄洛替尼联合吉西他滨放疗在治疗早期可显著抑制pEGFR(Y1173)和pAKT(S473),在治疗结束时可抑制pEGFR(Y845)、pEGFR(Y1173)和pAKT(S473)。本研究显示了表皮生长因子受体抑制反应中pEGFR(Y845)和pEGFR(Y1173)的新差异。
这些结果表明,表皮生长因子受体抑制剂西妥昔单抗和厄洛替尼可提高吉西他滨放疗的疗效。这项工作支持在胰腺癌临床试验中将表皮生长因子受体抑制剂与吉西他滨放疗联合应用。