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肿瘤微环境中的物理和化学梯度调节肿瘤细胞的侵袭、迁移和转移。

Physical and Chemical Gradients in the Tumor Microenvironment Regulate Tumor Cell Invasion, Migration, and Metastasis.

作者信息

Oudin Madeleine J, Weaver Valerie M

机构信息

Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.

Department of Surgery, Center for Bioengineering and Tissue Regeneration, University of California, San Francisco, San Francisco, California 94143.

出版信息

Cold Spring Harb Symp Quant Biol. 2016;81:189-205. doi: 10.1101/sqb.2016.81.030817. Epub 2017 Apr 19.

Abstract

Cancer metastasis requires the invasion of tumor cells into the stroma and the directed migration of tumor cells through the stroma toward the vasculature and lymphatics where they can disseminate and colonize secondary organs. Physical and biochemical gradients that form within the primary tumor tissue promote tumor cell invasion and drive persistent migration toward blood vessels and the lymphatics to facilitate tumor cell dissemination. These microenvironment cues include hypoxia and pH gradients, gradients of soluble cues that induce chemotaxis, and ions that facilitate galvanotaxis, as well as modifications to the concentration, organization, and stiffness of the extracellular matrix that produce haptotactic, alignotactic, and durotactic gradients. These gradients form through dynamic interactions between the tumor cells and the resident fibroblasts, adipocytes, nerves, endothelial cells, infiltrating immune cells, and mesenchymal stem cells. Malignant progression results from the integrated response of the tumor to these extrinsic physical and chemical cues. Here, we first describe how these physical and chemical gradients develop, and we discuss their role in tumor progression. We then review assays to study these gradients. We conclude with a discussion of clinical strategies used to detect and inhibit these gradients in tumors and of new intervention opportunities. Clarifying the role of these gradients in tumor evolution offers a unique approach to target metastasis.

摘要

癌症转移需要肿瘤细胞侵入基质,并通过基质向血管和淋巴管进行定向迁移,在那里它们可以扩散并定植于继发器官。原发肿瘤组织内形成的物理和生化梯度促进肿瘤细胞侵袭,并驱动其持续向血管和淋巴管迁移,以促进肿瘤细胞扩散。这些微环境线索包括缺氧和pH梯度、诱导趋化作用的可溶性线索梯度、促进电趋化作用的离子,以及细胞外基质浓度、组织和硬度的改变,这些改变会产生趋触性、排列趋化性和硬度趋化性梯度。这些梯度通过肿瘤细胞与驻留的成纤维细胞、脂肪细胞、神经、内皮细胞、浸润的免疫细胞和间充质干细胞之间的动态相互作用形成。恶性进展源于肿瘤对这些外在物理和化学线索的综合反应。在此,我们首先描述这些物理和化学梯度是如何形成的,并讨论它们在肿瘤进展中的作用。然后我们回顾研究这些梯度所使用的检测方法。我们最后讨论用于检测和抑制肿瘤中这些梯度的临床策略以及新的干预机会。阐明这些梯度在肿瘤演变中的作用为靶向转移提供了一种独特的方法。

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