Zhang Yu, Zhang Xiao Xi, Yuan Rui Yan, Ren Tai, Shao Zi Yu, Wang Hong Fei, Cai Wei Long, Chen Li Tian, Wang Xu An, Wang Ping
Shanghai Key Laboratory of Biliary Tract Disease Research, Xinhua Hospital, Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai 200092, People's Republic of China,
Department of General Surgery, Hangzhou First People's Hospital, Hangzhou 310006, People's Republic of China.
Onco Targets Ther. 2018 Aug 1;11:4479-4490. doi: 10.2147/OTT.S164670. eCollection 2018.
Cordycepin, the main active ingredient of a traditional Chinese herbal remedy - extracted from - has been demonstrated as a very effective anti-inflammatory and antitumor drug. The present study investigated its antitumor effect on pancreatic cancer, a highly aggressive cancer with extremely poor prognosis due to malignancy, and clarified its underlying mechanism both in vitro and in vivo.
The antitumor viability of cordycepin on human pancreatic cancer MIAPaCa-2 and Capan-1 cells was determined by colony formation assays. Annexin V/PI double staining and flow cytometry assay were used to investigate whether cordycepin induced apoptosis and cell cycle arrest. The mitochondrial membrane potential (ΔΨm) was analyzed by Rhodamine 123 staining, and expression of related proteins evaluated by Western blot and immunohistochemistry, both on pancreatic cancer cells and tumor xenografts to reveal the potential mechanism for the effect of cordycepin. Furthermore, the in vivo efficacy was examined on nude mice bearing MIAPaCa-2 cell tumors treated by intraperitoneal injection of cordycepin (0, 15, and 50 mg/kg/d) for 28 days.
Cordycepin inhibited cell viability, proliferation and colony formation ability and induced cell cycle arrest and early apoptosis of human pancreatic cancer cells (MIAPaCa-2 and Capan-1) in a dose- and time-dependent manner. The same effect was also observed in vivo. Decrease of ΔΨm and upregulation of Bax, cleaved caspase-3, cleaved caspase-9, and cleaved PARP as well as downregulation of Bcl-2 both in vitro and in vivo indicated that the mitochondria-mediated intrinsic pathway was involved in cordycepin's antitumor effect.
Our data showed that cordycepin inhibited the activity of pancreatic cancer both in vitro and in vivo by regulating apoptosis-related protein expression through the mitochondrial pathway and suggest that cordycepin may be a promising therapeutic option for pancreatic cancer.
虫草素是一种从传统中草药中提取的主要活性成分,已被证明是一种非常有效的抗炎和抗肿瘤药物。本研究调查了其对胰腺癌的抗肿瘤作用,胰腺癌是一种极具侵袭性的癌症,因其恶性程度高而预后极差,并阐明了其在体外和体内的潜在机制。
通过集落形成试验测定虫草素对人胰腺癌MIAPaCa-2和Capan-1细胞的抗肿瘤活力。采用膜联蛋白V/碘化丙啶双染和流式细胞术检测虫草素是否诱导细胞凋亡和细胞周期阻滞。用罗丹明123染色分析线粒体膜电位(ΔΨm),并用蛋白质免疫印迹法和免疫组织化学法评估相关蛋白在胰腺癌细胞和肿瘤异种移植中的表达,以揭示虫草素作用的潜在机制。此外,通过腹腔注射虫草素(0、15和50mg/kg/d)处理荷MIAPaCa-2细胞肿瘤的裸鼠28天,检测其体内疗效。
虫草素以剂量和时间依赖性方式抑制人胰腺癌细胞(MIAPaCa-2和Capan-1)的细胞活力增殖和集落形成能力,并诱导细胞周期阻滞和早期凋亡。在体内也观察到了同样的效果。体外和体内ΔΨm的降低以及Bax、裂解的caspase-3、裂解caspase-9和裂解的PARP的上调以及Bcl-2的下调表明线粒体介导的内源性途径参与了虫草素的抗肿瘤作用。
我们的数据表明,虫草素通过线粒体途径调节凋亡相关蛋白表达,在体外和体内均抑制胰腺癌的活性,提示虫草素可能是一种有前景的胰腺癌治疗选择。