Venetoclax Synergizes With Regorafenib for Colorectal Cancer by Targeting BCL-2.

IF 3.2 2区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Molecular Carcinogenesis Pub Date : 2025-10-01 Epub Date: 2025-07-24 DOI:10.1002/mc.70017
Lijun Zhu, Weicheng Wang, Yuwen Dong, Xiao Han, Wei Zhang, Zhonghua Zhang, Wenjie Guo, Yanhong Gu
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引用次数: 0

Abstract

Despite notable advancements in therapeutic modalities, many patients with colorectal cancer (CRC) exhibit inadequate response to regorafenib, largely due to the propensity for drug resistance. Deeper insights into the mechanism of CRC sensitivity to regorafenib therapy are urgently required. The antiapoptotic protein B-cell lymphoma 2 (BCL-2) is closely associated with a variety of malignancies. Therefore, this study investigated the role of BCL-2 in promoting regorafenib resistance in colorectal cancer. Venetoclax, a BCL-2 antagonist, potentiates the antitumor activity of regorafenib. The combination of regorafenib and Venetoclax inhibited the proliferation and promoted apoptosis of CRC cells and human umbilical vein endothelial cells in vitro by inhibiting tumor angiogenesis, promoting normalization of tumor blood vessels, and promoting immune cell infiltration and the release of immune cytotoxic factors. Although Venetoclax is primarily used clinically to treat hematological tumors, it has not yet been used to treat CRC. These findings provide new insights for the clinical treatment of CRC.

通过靶向BCL-2, Venetoclax与Regorafenib协同治疗结直肠癌
尽管治疗方式取得了显著进步,但许多结直肠癌(CRC)患者对瑞非尼的反应不足,这主要是由于耐药倾向。迫切需要更深入地了解结直肠癌对瑞非尼治疗敏感的机制。抗凋亡蛋白b细胞淋巴瘤2 (BCL-2)与多种恶性肿瘤密切相关。因此,本研究探讨BCL-2在促进结直肠癌瑞非尼耐药中的作用。Venetoclax是一种BCL-2拮抗剂,可增强reorafenib的抗肿瘤活性。regorafenib联合Venetoclax通过抑制肿瘤血管生成、促进肿瘤血管正常化、促进免疫细胞浸润和释放免疫细胞毒因子,在体外抑制结直肠癌细胞和人脐静脉内皮细胞增殖,促进细胞凋亡。虽然Venetoclax在临床上主要用于治疗血液系统肿瘤,但尚未用于治疗结直肠癌。这些发现为结直肠癌的临床治疗提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Carcinogenesis
Molecular Carcinogenesis 医学-生化与分子生物学
CiteScore
7.30
自引率
2.20%
发文量
112
审稿时长
2 months
期刊介绍: Molecular Carcinogenesis publishes articles describing discoveries in basic and clinical science of the mechanisms involved in chemical-, environmental-, physical (e.g., radiation, trauma)-, infection and inflammation-associated cancer development, basic mechanisms of cancer prevention and therapy, the function of oncogenes and tumors suppressors, and the role of biomarkers for cancer risk prediction, molecular diagnosis and prognosis.
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