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Ral相互作用蛋白76和血管内皮生长因子在肿瘤及卵巢黄体微环境中血管生成的潜在作用

The potential role of Ral-interacting protein 76 and vascular endothelial growth factor on angiogenesis in the tumor and ovarian corpus luteum microenvironment.

作者信息

Lee Seunghyung

机构信息

College of Animal Life Sciences, Kangwon National University, Chuncheon, Republic of Korea.

出版信息

Transl Cancer Res. 2024 Oct 31;13(10):5702-5710. doi: 10.21037/tcr-24-770. Epub 2024 Oct 17.

DOI:10.21037/tcr-24-770
PMID:39525031
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11543058/
Abstract

Tumors and the ovarian corpus luteum have complex mechanisms in the growth microenvironment. Angiogenesis is especially important for demonstrating the molecular mechanism of dynamic cellular function in tumors and corpus luteum. Angiogenesis in tumors and corpus luteum seems to have a similar function, and Ral-interacting protein 76 (RLIP76) and vascular endothelial growth factor (VEGF) are expressed in the tissues of tumors and ovarian corpus luteum. RLIP76 is a potential factor with VEGF in the tumor and corpus luteum angiogenesis. RLIP76 regulates a small GTPase (R-Ras) in cell survival, spreading, and migration. VEGF activates angiogenic functions in tumor and endothelial cells. Hypoxia-inducible factor-1 (HIF-1) is important in tumor growth, tumor angiogenesis, and corpus luteum. VEGF and HIF-1 regulate the angiogenic function of RLIP76, and RLIP76 controls vascular growth in endothelial and tumor cells. RLIP76, R-Ras, VEGF, and HIF-1 may be useful in the research of corpus luteum and cancer therapy and the study of mechanisms of tumor and corpus luteum angiogenesis. This review will help to elucidate the roles of RLIP76 and VEGF in tumor and corpus luteum angiogenesis, tumorigenesis, and the specific regulation of RLIP76 and VEGF. Thus, we reviewed the potential role of RLIP76 and VEGF in the angiogenesis of the tumor and corpus luteum in the tumor and ovarian microenvironment.

摘要

肿瘤和卵巢黄体在生长微环境中具有复杂的机制。血管生成对于阐明肿瘤和黄体中动态细胞功能的分子机制尤为重要。肿瘤和黄体中的血管生成似乎具有相似的功能,并且Ral相互作用蛋白76(RLIP76)和血管内皮生长因子(VEGF)在肿瘤组织和卵巢黄体中表达。RLIP76是肿瘤和黄体血管生成中与VEGF相关的一个潜在因子。RLIP76在细胞存活、扩散和迁移过程中调节一种小GTP酶(R-Ras)。VEGF激活肿瘤细胞和内皮细胞中的血管生成功能。缺氧诱导因子-1(HIF-1)在肿瘤生长、肿瘤血管生成和黄体中起重要作用。VEGF和HIF-1调节RLIP76的血管生成功能,而RLIP76控制内皮细胞和肿瘤细胞中的血管生长。RLIP76、R-Ras、VEGF和HIF-1可能在黄体研究、癌症治疗以及肿瘤和黄体血管生成机制的研究中具有应用价值。本综述将有助于阐明RLIP76和VEGF在肿瘤和黄体血管生成、肿瘤发生以及RLIP76和VEGF的具体调节中的作用。因此,我们综述了RLIP76和VEGF在肿瘤和卵巢微环境中肿瘤和黄体血管生成中的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb53/11543058/f9de2ab5c2fe/tcr-13-10-5702-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb53/11543058/4bf943a6ec47/tcr-13-10-5702-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb53/11543058/f9de2ab5c2fe/tcr-13-10-5702-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb53/11543058/4bf943a6ec47/tcr-13-10-5702-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb53/11543058/f9de2ab5c2fe/tcr-13-10-5702-f2.jpg

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