BITC使胰腺腺癌对trail诱导的细胞凋亡敏感。

C. A. Wicker, R. Sahu, Kashmira Kulkarni‐Datar, S. Srivastava, T. Brown
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引用次数: 28

摘要

胰腺腺癌是一种侵袭性癌症,诊断后死亡率大于95%,生存期短。化疗耐药性阻碍了成功的治疗。这种耐药性通常与K-Ras基因(K-Ras 12)密码子12的突变有关,这种基因突变存在于90%以上的胰腺腺癌中。密码子12突变使Ras处于组成性活性状态,导致细胞持续增殖。我们的研究确定了是否可以通过首先用异硫氰酸苄酯(BITC)敏化细胞来克服K-Ras 12突变的胰腺腺癌的TRAIL耐药。BITC是十字花科蔬菜的一种成分,是一种细胞周期抑制剂。检测BxPC3、MiaPaCa2和Panc-1人胰腺腺癌细胞株TRAIL耐药性。我们的研究表明,BITC通过双重激活外源性和内源性凋亡途径诱导TRAIL增敏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BITC Sensitizes Pancreatic Adenocarcinomas to TRAIL-induced Apoptosis.
Pancreatic adenocarcinoma is an aggressive cancer with a greater than 95% mortality rate and short survival after diagnosis. Chemotherapeutic resistance hinders successful treatment. This resistance is often associated with mutations in codon 12 of the K-Ras gene (K-Ras 12), which is present in over 90% of all pancreatic adenocarcinomas. Codon 12 mutations maintain Ras in a constitutively active state leading to continuous cellular proliferation. Our study determined if TRAIL resistance in pancreatic adenocarcinomas with K-Ras 12 mutations could be overcome by first sensitizing the cells with Benzyl isothiocyanate (BITC). BITC is a component of cruciferous vegetables and a cell cycle inhibitor. BxPC3, MiaPaCa2 and Panc-1 human pancreatic adenocarcinoma cell lines were examined for TRAIL resistance. Our studies show BITC induced TRAIL sensitization by dual activation of both the extrinsic and intrinsic apoptotic pathways.
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