Chang Tammy T, Thakar Dhruv, Weaver Valerie M
Department of Surgery, University of California, San Francisco, San Francisco, CA 94143, USA; Liver Center, University of California, San Francisco, San Francisco, CA 94143, USA.
Department of Surgery, University of California, San Francisco, San Francisco, CA 94143, USA; Center for Bioengineering and Tissue Regeneration, University of California San Francisco, San Francisco, CA 94143, USA.
Matrix Biol. 2017 Jan;57-58:178-189. doi: 10.1016/j.matbio.2016.12.005. Epub 2016 Dec 23.
Clinically, non-invasive carcinomas are confined to the epithelial side of the basement membrane and are classified as benign, whereas invasive cancers invade through the basement membrane and thereby acquire the potential to metastasize. Recent findings suggest that, in addition to protease-mediated degradation and chemotaxis-stimulated migration, basement membrane invasion by malignant cells is significantly influenced by the stiffness of the associated interstitial extracellular matrix and the contractility of the tumor cells that is dictated in part by their oncogenic genotype. In this review, we highlight recent findings that illustrate unifying molecular mechanisms whereby these physical cues contribute to tissue fibrosis and malignancy in three epithelial organs: breast, pancreas, and liver. We also discuss the clinical implications of these findings and the biological properties and clinical challenges linked to the unique biology of each of these organs.
临床上,非侵袭性癌局限于基底膜的上皮侧,被归类为良性,而侵袭性癌则穿过基底膜,从而获得转移的潜能。最近的研究结果表明,除了蛋白酶介导的降解和趋化性刺激的迁移外,恶性细胞对基底膜的侵袭还受到相关间质细胞外基质硬度以及肿瘤细胞收缩性的显著影响,而肿瘤细胞的收缩性部分由其致癌基因型决定。在本综述中,我们重点介绍了最近的研究结果,这些结果阐明了统一的分子机制,通过这些机制,这些物理信号在三个上皮器官(乳腺、胰腺和肝脏)中促成组织纤维化和恶性肿瘤。我们还讨论了这些研究结果的临床意义以及与这些器官各自独特生物学相关的生物学特性和临床挑战。