Angiogenesis causes and vasculogenic mimicry formation in the context of cancer stem cells

IF 9.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et biophysica acta. Reviews on cancer Pub Date : 2025-04-15 DOI:10.1016/j.bbcan.2025.189323
Ying Li , Xiaofang Liu , Yaodong Dong , Yingying Zhou
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Abstract

Tumor occurrence, development, invasion, and metastasis are regulated by multiple mechanisms. Among these, angiogenesis promotes tumor progression mainly by supplying tumor tissue and providing channels for tumor metastasis. Cancer stem cells (CSCs) are another important factor affecting tumor progression by involving in tumor initiation and development, while remaining insensitive to conventional antitumor treatments. Among treatment strategies for them, owing to the existence of alternative angiogenic pathways or the risk of damaging normal stem cells, the clinical effect is not ideal. Angiogenesis and CSCs may influence each other in this process. Tumor angiogenesis can support CSC self-renewal by providing a suitable microenvironment, whereas CSCs can regulate tumor neovascularization and mediate drug resistance to anti-angiogenic therapy. This review summarized the role of vascular niche formed by angiogenesis in CSC self-renewal and stemness maintenance, and the function of CSCs in endothelial progenitor cell differentiation and pro-angiogenic factor upregulation. We also elucidated the malignant loop between CSCs and angiogenesis promoting tumor progression. Additionally, we summarized and proposed therapeutic targets, including blocking tumor-derived endothelial differentiation, inhibiting pro-angiogenic factor upregulation, and directly targeting endothelial-like cells comprising CSCs. And we analyzed the feasibility of these strategies to identify more effective methods to improve tumor treatment.

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肿瘤干细胞血管生成的原因和血管生成模拟的形成
肿瘤的发生、发展、侵袭和转移受多种机制的调控。其中血管生成主要通过供给肿瘤组织和提供肿瘤转移通道来促进肿瘤进展。肿瘤干细胞(CSCs)是影响肿瘤进展的另一个重要因素,它参与肿瘤的发生和发展,同时对传统的抗肿瘤治疗不敏感。在治疗策略中,由于存在替代血管生成途径或有损伤正常干细胞的风险,临床效果并不理想。在此过程中血管生成与CSCs可能相互影响。肿瘤血管生成可以通过提供合适的微环境支持CSC自我更新,而CSC可以调节肿瘤新生血管并介导抗血管生成治疗的耐药。本文就血管生成形成的血管生态位在CSC自我更新和干细胞维持中的作用,以及CSC在内皮祖细胞分化和促血管生成因子上调中的作用作一综述。我们还阐明了CSCs与促进肿瘤进展的血管生成之间的恶性循环。此外,我们总结并提出了治疗靶点,包括阻断肿瘤来源的内皮细胞分化,抑制促血管生成因子上调,直接靶向内皮样细胞包括CSCs。我们分析了这些策略的可行性,以确定更有效的方法来改善肿瘤治疗。
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来源期刊
Biochimica et biophysica acta. Reviews on cancer
Biochimica et biophysica acta. Reviews on cancer 医学-生化与分子生物学
CiteScore
17.20
自引率
0.00%
发文量
138
审稿时长
33 days
期刊介绍: Biochimica et Biophysica Acta (BBA) - Reviews on Cancer encompasses the entirety of cancer biology and biochemistry, emphasizing oncogenes and tumor suppressor genes, growth-related cell cycle control signaling, carcinogenesis mechanisms, cell transformation, immunologic control mechanisms, genetics of human (mammalian) cancer, control of cell proliferation, genetic and molecular control of organismic development, rational anti-tumor drug design. It publishes mini-reviews and full reviews.
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