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肿瘤微环境产生的酸度会促进局部浸润。

Acidity generated by the tumor microenvironment drives local invasion.

机构信息

Departments of Cancer Imaging and Metabolism, Radiology, and Analytic Microscopy Laboratory, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.

出版信息

Cancer Res. 2013 Mar 1;73(5):1524-35. doi: 10.1158/0008-5472.CAN-12-2796. Epub 2013 Jan 3.


DOI:10.1158/0008-5472.CAN-12-2796
PMID:23288510
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3594450/
Abstract

The pH of solid tumors is acidic due to increased fermentative metabolism and poor perfusion. It has been hypothesized that acid pH promotes local invasive growth and metastasis. The hypothesis that acid mediates invasion proposes that H(+) diffuses from the proximal tumor microenvironment into adjacent normal tissues where it causes tissue remodeling that permits local invasion. In the current work, tumor invasion and peritumoral pH were monitored over time using intravital microscopy. In every case, the peritumoral pH was acidic and heterogeneous and the regions of highest tumor invasion corresponded to areas of lowest pH. Tumor invasion did not occur into regions with normal or near-normal extracellular pH. Immunohistochemical analyses revealed that cells in the invasive edges expressed the glucose transporter-1 and the sodium-hydrogen exchanger-1, both of which were associated with peritumoral acidosis. In support of the functional importance of our findings, oral administration of sodium bicarbonate was sufficient to increase peritumoral pH and inhibit tumor growth and local invasion in a preclinical model, supporting the acid-mediated invasion hypothesis. Cancer Res; 73(5); 1524-35. ©2012 AACR.

摘要

由于发酵代谢增加和灌注不良,实体瘤的 pH 值呈酸性。有人假设酸性 pH 值促进局部侵袭性生长和转移。酸介导侵袭的假设提出,H(+) 从近端肿瘤微环境扩散到相邻的正常组织,导致组织重塑,从而允许局部侵袭。在当前的工作中,使用活体显微镜监测肿瘤侵袭和肿瘤周围 pH 值随时间的变化。在每种情况下,肿瘤周围 pH 值均呈酸性且不均匀,侵袭性最强的区域与 pH 值最低的区域相对应。肿瘤不会侵袭到正常或接近正常的细胞外 pH 值区域。免疫组织化学分析显示,侵袭边缘的细胞表达葡萄糖转运蛋白-1 和钠-氢交换器-1,两者均与肿瘤周围酸中毒有关。支持我们研究结果的功能重要性,口服碳酸氢钠足以增加肿瘤周围 pH 值并抑制临床前模型中的肿瘤生长和局部侵袭,支持酸介导的侵袭假说。Cancer Res; 73(5); 1524-35. ©2012 AACR.

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本文引用的文献

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Cancer Res. 2012-6-19

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