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肿瘤相关周细胞:致瘤性与癌症治疗靶点

Tumor-Associated Pericytes: Tumorigenicity and Targeting for Cancer Therapy.

作者信息

Tan Jiale, Yu Zihang, Pi Ruozheng, Lin Yan, Wang Wei, Chen Minfeng, Bai Xue

机构信息

Department of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.

The First School of Clinical Medicine, Southern Medical University, Guangzhou, China.

出版信息

Curr Vasc Pharmacol. 2025 Feb 19. doi: 10.2174/0115701611365339250213101338.

Abstract

Pericytes, also known as mural cells, are cells embedded between endothelial cells and the basement membrane of capillaries, where they orchestrate the morphological and functional homeostasis of blood vessels. Within the tumor microenvironment, pericytes interact closely with various cellular components, including tumor cells, stromal cells, and immune cells. Through these dynamic interactions, pericytes are activated and subsequently transform into tumor-associated pericytes (TPCs). The origin of TPCs varies depending on the tissue and tumor type, contributing to their phenotypic and functional heterogeneity. TPCs play pivotal roles in facilitating tumor progression, metastasis, immune evasion, and therapeutic resistance by promoting angiogenesis, engaging in reciprocal interactions with tumor cells, remodeling the extracellular matrix, and fostering an immunosuppressive microenvironment. This review synthesizes the latest significant advancements in targeted therapies against TPCs. It underscores the challenges inherent in developing effective anti-TPC therapies, which include the heterogeneity and pluripotency of TPCs, the absence of specific markers for precise TPC targeting, and the limited understanding of how current anti-tumor therapies affect TPCs and vice versa. This review furnishes a comprehensive understanding of the origins, markers, and functions of TPCs, and their interplays within the tumor microenvironment, providing prospective strategies for more effective anti-tumor therapy.

摘要

周细胞,也称为壁细胞,是嵌入在毛细血管内皮细胞和基底膜之间的细胞,在那里它们协调血管的形态和功能稳态。在肿瘤微环境中,周细胞与各种细胞成分密切相互作用,包括肿瘤细胞、基质细胞和免疫细胞。通过这些动态相互作用,周细胞被激活,随后转变为肿瘤相关周细胞(TPC)。TPC的起源因组织和肿瘤类型而异,这导致了它们的表型和功能异质性。TPC通过促进血管生成、与肿瘤细胞进行相互作用、重塑细胞外基质以及营造免疫抑制微环境,在促进肿瘤进展、转移、免疫逃逸和治疗抵抗方面发挥关键作用。本综述综合了针对TPC的靶向治疗的最新重大进展。它强调了开发有效的抗TPC疗法所固有的挑战,包括TPC的异质性和多能性、缺乏精确靶向TPC的特异性标志物,以及对当前抗肿瘤疗法如何影响TPC以及反之亦然的了解有限。本综述全面介绍了TPC的起源、标志物和功能,以及它们在肿瘤微环境中的相互作用,为更有效的抗肿瘤治疗提供了前瞻性策略。

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