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[用奥布利森(bcl-2反义寡核苷酸)进行促凋亡治疗——临床前和临床结果综述]

[Proapoptotic therapy with oblimersen (bcl-2 antisense oligonucleotide)--review of preclinical and clinical results].

作者信息

Büchele T

机构信息

Aventis Pharma Deutschland GmbH, Geschäftseinheit Onkologie, Bad Soden am Taunus.

出版信息

Onkologie. 2003 Dec;26 Suppl 7:60-9. doi: 10.1159/000076177.

Abstract

The regulation of apoptosis is an important potential target for anticancer therapy. The mitochondrial Bcl-2 protein inhibits apoptosis and is therefore an important mediator of resistance to treatment with traditional cytotoxic chemotherapy, radiotherapy and monoclonal antibody therapy. Oblimersen (Genasense, Aventis Pharmaceuticals / Genta Inc) is a 18mer antisense-oligonucleotide (ASO), which specifically binds to the first 6 codons of the human bcl-2 mRNA, resulting in degradation and destruction of the mRNA by RNAse H. Subsequently there is a significant decrease of bcl-2 translation. A growing number of preclinical and clinical studies suggests that the combination of cytotoxic therapy with Oblimersen results in synergistic anticancer efficacy in many hematologic and solid tumors. Due to its low toxicity profile, oblimersen is an ideal combination partner with conventional chemotherapy. Three randomized phase-III trials (malignant melanoma, chronic lymphocytic leukemia, multiple myeloma) have recently finished recruitment. The results of these studies will be available by the end of 2003. Based on preclinical data, a lot of nonrandomized phase-II studies on several different tumor types like AML, CML, NHL, prostate cancer and breast cancer are underway. The manipulation of proapoptotic and antiapoptotic factors in favor of proapoptotic factors by inhibition of the bcl-2 protein translation in order to enhance the efficacy of anticancer treatments represents a promising new treatment concept in oncology.

摘要

细胞凋亡的调控是抗癌治疗的一个重要潜在靶点。线粒体Bcl-2蛋白可抑制细胞凋亡,因此是对传统细胞毒性化疗、放疗及单克隆抗体治疗产生耐药性的重要介导因子。奥布利默森(Genasense,安万特制药公司/根他公司)是一种18聚体反义寡核苷酸(ASO),它能特异性结合人bcl-2 mRNA的前6个密码子,导致mRNA被RNA酶H降解破坏。随后,bcl-2的翻译显著减少。越来越多的临床前和临床研究表明,细胞毒性治疗与奥布利默森联合使用在许多血液系统肿瘤和实体瘤中具有协同抗癌效果。由于其低毒性,奥布利默森是传统化疗的理想联合用药伙伴。三项随机III期试验(恶性黑色素瘤、慢性淋巴细胞白血病、多发性骨髓瘤)最近已完成入组。这些研究结果将于2003年底公布。基于临床前数据,许多针对几种不同肿瘤类型(如急性髓细胞白血病、慢性髓细胞白血病、非霍奇金淋巴瘤、前列腺癌和乳腺癌)的非随机II期研究正在进行。通过抑制bcl-2蛋白翻译来调控促凋亡和抗凋亡因子,使其有利于促凋亡因子,从而提高抗癌治疗效果,这代表了肿瘤学中一个有前景的新治疗理念。

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