Kim Ryungsa, Emi Manabu, Tanabe Kazuaki, Toge Tetsuya
Department of Surgical Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
Cancer. 2004 Dec 1;101(11):2491-502. doi: 10.1002/cncr.20696.
Bcl-2 protein plays a critical role in inhibiting anticancer drug-induced apoptosis, which is mediated by a mitochondria-dependent pathway that controls the release of cytochrome c from mitochondria through anion channels. Constitutive overexpression of Bcl-2 or unchanged expression after treatment with anticancer drugs confers drug resistance not only to hematologic malignancies but also to solid tumors. The down-regulation of Bcl-2 protein by the antisense (AS) Bcl-2 (oblimesen sodium) may be a useful method for targeting the antiapoptotic protein and thereby increasing the chemotherapeutic effect of anticancer drugs. Several randomized, controlled, Phase III trials have compared standard chemotherapy with a combination of AS Bcl-2 and standard chemotherapy for the treatment of patients with chronic lymphocytic leukemia, multiple myeloma, malignant melanoma, and nonsmall cell lung carcinoma. Nonrandomized clinical trials and preclinical evaluations of AS Bcl-2 also are underway for patients with other malignancies. Here, the authors review the current clinical and preclinical evaluations of AS Bcl-2 and discuss its potential to act as a chemosensitizer and to enhance the therapeutic effect of cancer chemotherapy.
Bcl-2蛋白在抑制抗癌药物诱导的细胞凋亡中起关键作用,这种凋亡由线粒体依赖性途径介导,该途径通过阴离子通道控制细胞色素c从线粒体的释放。Bcl-2的组成性过表达或抗癌药物治疗后表达不变,不仅赋予血液系统恶性肿瘤耐药性,也赋予实体瘤耐药性。反义(AS)Bcl-2(奥布利森钠)下调Bcl-2蛋白可能是靶向抗凋亡蛋白从而提高抗癌药物化疗效果的一种有用方法。几项随机对照III期试验比较了标准化疗与AS Bcl-2联合标准化疗治疗慢性淋巴细胞白血病、多发性骨髓瘤、恶性黑色素瘤和非小细胞肺癌患者的疗效。针对其他恶性肿瘤患者的AS Bcl-2非随机临床试验和临床前评估也在进行中。在此,作者综述了AS Bcl-2目前的临床和临床前评估,并讨论了其作为化学增敏剂及增强癌症化疗疗效的潜力。