Frankel Stanley R
Department of Medicine, Greenebaum Cancer Center, University of Maryland at Baltimore, Baltimore, MD, USA.
Semin Oncol. 2003 Apr;30(2):300-4. doi: 10.1053/sonc.2003.50041.
The components of the apoptotic pathway are targets for anticancer therapy. Bcl-2 protein inhibits apoptosis and confers resistance to treatment with traditional cytotoxic chemotherapy, radiotherapy, and monoclonal antibodies. Oblimersen sodium (G3139, Genasense, Genta Inc, Berkeley Heights, NJ) is an antisense oligonucleotide compound designed to specifically bind to the first six codons of the human bcl-2 mRNA sequence, resulting in degradation of bcl-2 mRNA and subsequent decrease in Bcl-2 protein translation. Oblimersen is the first oligonucleotide to demonstrate proof of principle of an antisense effect in human tumors by the documented downregulation of the target Bcl-2 protein. A growing body of preclinical and clinical evidence suggests that oblimersen synergizes with many cytotoxic and biologic/immunotherapeutic agents against a variety of hematologic malignancies and solid tumors. Randomized clinical trials are currently underway to evaluate the efficacy and tolerability of oblimersen in combination with cytotoxic chemotherapy in chronic lymphocytic leukemia (CLL), multiple myeloma (MM), malignant melanoma, and non-small cell lung cancer. In addition, nonrandomized trials are underway to evaluate oblimersen in non-Hodgkin's lymphoma (NHL), acute myeloid leukemia (AML), and hormone-refractory prostate cancer. Preclinical data support the clinical evaluation of oblimersen in additional tumor types, including chronic myelogenous leukemia, and breast, small cell lung, gastric, colon, bladder (CML), and Merkel cell cancers. Enhancement of the efficacy of anticancer treatments with oblimersen Bcl-2 antisense therapy represents a promising new apoptosis-modulating strategy, and ongoing clinical trials will test this therapeutic approach.
凋亡途径的组成部分是抗癌治疗的靶点。Bcl-2蛋白可抑制细胞凋亡,并赋予对传统细胞毒性化疗、放疗及单克隆抗体治疗的抗性。奥布利默森钠(G3139,Genasense,根塔公司,新泽西州伯克利高地)是一种反义寡核苷酸化合物,设计用于特异性结合人bcl-2 mRNA序列的前六个密码子,导致bcl-2 mRNA降解,随后Bcl-2蛋白翻译减少。奥布利默森是首个通过记录的靶标Bcl-2蛋白下调,在人类肿瘤中证明反义效应原理的寡核苷酸。越来越多的临床前和临床证据表明,奥布利默森可与多种细胞毒性和生物/免疫治疗药物协同作用,对抗多种血液系统恶性肿瘤和实体瘤。目前正在进行随机临床试验,以评估奥布利默森联合细胞毒性化疗治疗慢性淋巴细胞白血病(CLL)、多发性骨髓瘤(MM)、恶性黑色素瘤和非小细胞肺癌的疗效和耐受性。此外,正在进行非随机试验,以评估奥布利默森在非霍奇金淋巴瘤(NHL)、急性髓性白血病(AML)和激素难治性前列腺癌中的作用。临床前数据支持对奥布利默森在其他肿瘤类型中的临床评估,包括慢性粒细胞白血病以及乳腺癌、小细胞肺癌、胃癌、结肠癌、膀胱癌(CML)和默克尔细胞癌。用奥布利默森Bcl-2反义疗法提高抗癌治疗的疗效代表了一种有前景的新的凋亡调节策略,正在进行的临床试验将检验这种治疗方法。