Wiśniewska Weronika, Kopka Michał, Siemiątkowska Karolina, Fudalej Marta Magdalena, Sobiborowicz Aleksandra, Badowska-Kozakiewicz Anna Maria
Students' Scientific Organization of Cancer Cell Biology, Department of Cancer Prevention, Medical University of Warsaw, Warsaw, Poland.
Department of Cancer Prevention, Medical University of Warsaw, Warsaw, Poland.
Contemp Oncol (Pozn). 2021;25(1):33-44. doi: 10.5114/wo.2021.105075. Epub 2021 Apr 15.
Tumour angiogenesis is a crucial factor associated with tumour growth, progression, and metastasis. The whole process is the result of an interaction between a wide range of different molecules, influencing each other. Herein we summarize novel discoveries related to the less known angiogenic molecules such as galectins, pentraxin-3, Ral-interacting protein of 76 kDa (RLIP76), long non-coding RNAs (lncRNAs), B7-H3, and delta-like ligand-4 (DLL-4) and their role in the process of tumour angiogenesis. These molecules influence the most important molecular pathways involved in the formation of blood vessels in cancer, including the vascular endothelial growth factor (VEGF)-vascular endothelial growth factor receptor interaction (VEGFR), HIF1-a activation, or PI3K/Akt/mTOR and JAK-STAT signalling pathways. Increased expression of galectins, RLIP76, and B7H3 has been proven in several malignancies. Pentraxin-3, which appears to inhibit tumour angiogenesis, shows reduced expression in tumour tissues. Anti-angiogenic treatment based mainly on VEGF inhibition has proved to be of limited effectiveness, leading to the development of drug resistance. The newly discovered molecules are of great interest as a potential source of new anti-cancer therapies. Their role as targets for new drugs and as prognostic markers in neoplasms is discussed in this review.
肿瘤血管生成是与肿瘤生长、进展和转移相关的关键因素。整个过程是多种不同分子相互作用的结果,这些分子相互影响。在此,我们总结了与半乳凝素、五聚体蛋白3、76 kDa的Ral相互作用蛋白(RLIP76)、长链非编码RNA(lncRNA)、B7-H3和δ样配体4(DLL-4)等鲜为人知的血管生成分子相关的新发现,以及它们在肿瘤血管生成过程中的作用。这些分子影响癌症中血管形成所涉及的最重要分子途径,包括血管内皮生长因子(VEGF)-血管内皮生长因子受体相互作用(VEGFR)、HIF1-α激活或PI3K/Akt/mTOR和JAK-STAT信号通路。在几种恶性肿瘤中已证实半乳凝素、RLIP76和B7H3的表达增加。似乎抑制肿瘤血管生成的五聚体蛋白3在肿瘤组织中的表达降低。主要基于VEGF抑制的抗血管生成治疗已被证明效果有限,导致耐药性的产生。新发现的分子作为潜在的新型抗癌治疗来源备受关注。本文综述了它们作为新药靶点和肿瘤预后标志物的作用。