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肿瘤微环境中的血管生成和淋巴管生成级联反应。

Angiogenic and lymphangiogenic cascades in the tumor microenvironment.

作者信息

Onimaru Mitsuho, Yonemitsu Yoshikazu

机构信息

Division of Pathophysiological and Experimental Pathology, Department of Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Front Biosci (Schol Ed). 2011 Jan 1;3(1):216-25. doi: 10.2741/s146.

Abstract

Blood and lymphatic vessels in tumor tissue are major components of the tumor microenvironment. These vessels are newly formed from pre-existing host vessels stimulated by pro-blood-angiogenic and pro-lymph-angiogenic (pro-blood/lymph-angiogenic) factors expressed in tumor cells. Tumor cells establish a specific stromal microenvironment fostering tumor growth, in which blood/lymph-angiogenesis are involved. The tumor-associated blood/lymph-angiogenesis is continually induced by complicated cytokine networks, namely pro-blood/lymph-angiogenic factor-mediated paracrine and autocrine interactions among tumor cells and stromal cells including endothelial cells (ECs) and non-endothelial mesenchymal cells (neMCs). In this review, we provide an overview of the features of tumor-associated blood/lymph-angiogenesis based on recent and updated information obtained mainly from our studies. With regard to the constituent cell-dependent molecular mechanisms that regulate tumor blood/lymph-angiogenesis, we focus on: 1) the role of blood/lymph-angiogenesis-related factors/receptors expressed in tumor cells; and 2) the role of blood/lymph-angiogenesis-related factors/receptors expressed in stromal cells (ECs and neMCs). Finally, we discuss the features of tumor-associated blood/lymph-anigogenesis, especially a vessel abnormality through the viewpoint of blood/lymph-angiogenic cascades in tumor microenvironment for better understanding of the tumor vascular biology.

摘要

肿瘤组织中的血管和淋巴管是肿瘤微环境的主要组成部分。这些血管由肿瘤细胞中表达的促血管生成和促淋巴管生成(促血/淋巴管生成)因子刺激已有的宿主血管新生而成。肿瘤细胞建立了促进肿瘤生长的特定基质微环境,其中涉及血/淋巴管生成。肿瘤相关的血/淋巴管生成由复杂的细胞因子网络持续诱导,即促血/淋巴管生成因子介导的肿瘤细胞与包括内皮细胞(ECs)和非内皮间充质细胞(neMCs)在内的基质细胞之间的旁分泌和自分泌相互作用。在本综述中,我们基于主要从我们的研究中获得的最新信息,概述肿瘤相关血/淋巴管生成的特征。关于调节肿瘤血/淋巴管生成的依赖于组成细胞的分子机制,我们重点关注:1)肿瘤细胞中表达的血/淋巴管生成相关因子/受体的作用;2)基质细胞(ECs和neMCs)中表达的血/淋巴管生成相关因子/受体的作用。最后,我们讨论肿瘤相关血/淋巴管生成的特征,特别是从肿瘤微环境中血/淋巴管生成级联反应的角度探讨血管异常,以便更好地理解肿瘤血管生物学。

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