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靶向治疗慢性淋巴细胞白血病和其他血液系统恶性肿瘤中的 BCL2。

Targeting BCL2 in Chronic Lymphocytic Leukemia and Other Hematologic Malignancies.

机构信息

Department of Leukemia, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd., Unit 428, Houston, TX, 77030, USA.

出版信息

Drugs. 2019 Aug;79(12):1287-1304. doi: 10.1007/s40265-019-01163-4.

Abstract

Apoptosis, the process of programmed cell death, occurs normally during development and aging. Members of the B-cell lymphoma 2 (BCL2) family of proteins are central regulators of apoptosis, and resistance to apoptosis is one of the hallmarks of cancer. Targeting the apoptotic pathway via BCL2 inhibitors has been considered a promising treatment strategy in the past decade. Initial efforts with small molecule BH3 mimetics such as ABT-737 and ABT-263 (navitoclax) pioneered the development of the first-in-class Food and Drug Administration (FDA)-approved oral BCL2 inhibitor, venetoclax. Venetoclax was approved for the treatment of chronic lymphocytic leukemia and acute myeloid leukemia, and is now being studied in a number of hematologic malignancies. Several other inhibitors targeting different BCL2 family members are now in early stages of development.

摘要

细胞凋亡是一种程序性细胞死亡的过程,正常发生于发育和衰老过程中。B 细胞淋巴瘤 2(BCL2)家族蛋白是细胞凋亡的核心调节因子,而对细胞凋亡的抵抗是癌症的一个标志。在过去十年中,通过 BCL2 抑制剂靶向细胞凋亡途径被认为是一种有前途的治疗策略。最初使用小分子 BH3 模拟物,如 ABT-737 和 ABT-263(navitoclax),开创了首个 FDA 批准的口服 BCL2 抑制剂 venetoclax 的发展。Venetoclax 被批准用于治疗慢性淋巴细胞白血病和急性髓细胞白血病,目前正在许多血液恶性肿瘤中进行研究。目前还有几种针对不同 BCL2 家族成员的其他抑制剂处于早期开发阶段。

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