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肿瘤微环境中血管生成剂与抗血管生成剂的研究进展

Progress on angiogenic and antiangiogenic agents in the tumor microenvironment.

作者信息

Xu Jian, Tang Zhihua

机构信息

Department of Pharmacy, Shaoxing People's Hospital, Shaoxing, China.

出版信息

Front Oncol. 2024 Nov 19;14:1491099. doi: 10.3389/fonc.2024.1491099. eCollection 2024.

Abstract

The development of tumors and their metastasis relies heavily on the process of angiogenesis. When the volume of a tumor expands, the resulting internal hypoxic conditions trigger the body to enhance the production of various angiogenic factors. These include vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF), platelet-derived growth factor (PDGF), and transforming growth factor-α (TGF-α), all of which work together to stimulate the activation of endothelial cells and catalyze angiogenesis. Antiangiogenic therapy (AAT) aims to normalize tumor blood vessels by inhibiting these angiogenic signals. In this review, we will explore the molecular mechanisms of angiogenesis within the tumor microenvironment, discuss traditional antiangiogenic drugs along with their limitations, examine new antiangiogenic drugs and the advantages of combination therapy, and consider future research directions in the field of antiangiogenic drugs. This comprehensive overview aims to provide insights that may aid in the development of more effective anti-tumor treatments.

摘要

肿瘤的发生及其转移在很大程度上依赖于血管生成过程。当肿瘤体积增大时,由此产生的内部缺氧状态会促使机体增加各种血管生成因子的产生。这些因子包括血管内皮生长因子(VEGF)、成纤维细胞生长因子(FGF)、血小板衍生生长因子(PDGF)和转化生长因子-α(TGF-α),它们共同作用以刺激内皮细胞的活化并催化血管生成。抗血管生成疗法(AAT)旨在通过抑制这些血管生成信号使肿瘤血管正常化。在本综述中,我们将探讨肿瘤微环境中血管生成的分子机制,讨论传统抗血管生成药物及其局限性,研究新型抗血管生成药物以及联合治疗的优势,并思考抗血管生成药物领域未来的研究方向。这一全面概述旨在提供有助于开发更有效抗肿瘤治疗方法的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9366/11611712/daf587301282/fonc-14-1491099-g001.jpg

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