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BCL-2抑制剂维奈托克治疗反应的潜在生物标志物:现状与未来方向

Potential Biomarkers for Treatment Response to the BCL-2 Inhibitor Venetoclax: State of the Art and Future Directions.

作者信息

Salah Haneen T, DiNardo Courtney D, Konopleva Marina, Khoury Joseph D

机构信息

College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Cancers (Basel). 2021 Jun 14;13(12):2974. doi: 10.3390/cancers13122974.

Abstract

Intrinsic apoptotic pathway dysregulation plays an essential role in all cancers, particularly hematologic malignancies. This role has led to the development of multiple therapeutic agents targeting this pathway. Venetoclax is a selective BCL-2 inhibitor that has been approved for the treatment of chronic lymphoid leukemia and acute myeloid leukemia. Given the reported resistance to venetoclax, understanding the mechanisms of resistance and the potential biomarkers of response is crucial to ensure optimal drug usage and improved patient outcomes. Mechanisms of resistance to venetoclax include alterations involving the BH3-binding groove, gene mutations affecting venetoclax binding, and activation of alternative anti-apoptotic pathways. Moreover, various potential genetic biomarkers of venetoclax resistance have been proposed, including chromosome 17p deletion, trisomy 12, and loss or mutation. This manuscript provides an overview of biomarkers that could predict treatment response to venetoclax.

摘要

内源性凋亡途径失调在所有癌症中都起着至关重要的作用,尤其是血液系统恶性肿瘤。这一作用促使了多种靶向该途径的治疗药物的研发。维奈克拉是一种选择性BCL-2抑制剂,已被批准用于治疗慢性淋巴细胞白血病和急性髓系白血病。鉴于报道的对维奈克拉的耐药性,了解耐药机制和潜在的反应生物标志物对于确保最佳药物使用和改善患者预后至关重要。对维奈克拉的耐药机制包括涉及BH3结合凹槽的改变、影响维奈克拉结合的基因突变以及替代抗凋亡途径的激活。此外,已经提出了各种潜在的维奈克拉耐药基因生物标志物,包括17号染色体短臂缺失、三体12以及缺失或突变。本手稿概述了可预测对维奈克拉治疗反应的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7896/8231978/4045ab221e83/cancers-13-02974-g001.jpg

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