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肿瘤-基质相互作用:癌症相关成纤维细胞作为抗癌治疗的新靶点?

Tumour-stroma interaction: cancer-associated fibroblasts as novel targets in anti-cancer therapy?

作者信息

Micke Patrick, Ostman Arne

机构信息

Ludwig Institute for Cancer Research, Uppsala, Sweden.

出版信息

Lung Cancer. 2004 Aug;45 Suppl 2:S163-75. doi: 10.1016/j.lungcan.2004.07.977.

Abstract

Stroma cells, together with extracellular matrix components, provide the microenvironment that is pivotal for cancer cell growth, invasion and metastatic progression. Characteristic stroma alterations accompany or even precede the malignant conversion of epithelial cells. Crucial in this process are fibroblasts, also termed myofibroblasts or cancer-associated fibroblasts (CAFs) that are located in the vicinity of the neoplastic epithelial cells. They are able to modify the phenotype of the epithelial cells by direct cell-to-cell contacts, through soluble factors or by modification of extracellular matrix components. Seminal functional studies in various cancer types, including breast, colon, prostate and lung cancer, have confirmed the concept that fibroblasts can determine the fate of the epithelial cell, since they are able to promote malignant conversion as well as to revert tumour cells to a normal phenotype. This review focuses on characteristic changes of fibroblasts in cancer and provides the experimental background elucidating functional properties of CAFs in the carcinogenic process. A possible implication in lung carcinogenesis is emphasised. Finally, a laser-capture- and microarray-based approach is presented, which comprehensively characterises carcinoma-associated fibroblasts in their in vivo environment for the identification of potential targets for anti-cancer therapy.

摘要

基质细胞与细胞外基质成分共同构成了对癌细胞生长、侵袭和转移进程至关重要的微环境。特征性的基质改变伴随着上皮细胞的恶性转化,甚至在此之前就已出现。在此过程中起关键作用的是成纤维细胞,也称为肌成纤维细胞或癌症相关成纤维细胞(CAFs),它们位于肿瘤上皮细胞附近。它们能够通过直接的细胞间接触、可溶性因子或细胞外基质成分的修饰来改变上皮细胞的表型。包括乳腺癌、结肠癌、前列腺癌和肺癌在内的各种癌症类型的开创性功能研究证实了成纤维细胞能够决定上皮细胞命运的概念,因为它们既能促进恶性转化,也能使肿瘤细胞恢复正常表型。本综述聚焦于癌症中,成纤维细胞的特征性变化,并提供了阐明CAFs在致癌过程中功能特性的实验背景。强调了其在肺癌发生中的可能影响。最后,介绍了一种基于激光捕获和微阵列的方法,该方法全面表征了体内环境中的癌相关成纤维细胞,以识别抗癌治疗的潜在靶点。

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