Suppr超能文献

乳腺癌进展中的细胞极性蛋白

Cell Polarity Proteins in Breast Cancer Progression.

作者信息

Rejon Carlis, Al-Masri Maia, McCaffrey Luke

机构信息

Division of Experimental Medicine, Department of Oncology, Rosalind and Morris Goodman Cancer Research Centre, McGill University, Montreal, Canada.

出版信息

J Cell Biochem. 2016 Oct;117(10):2215-23. doi: 10.1002/jcb.25553. Epub 2016 Jun 30.

Abstract

Breast cancer, one of the leading causes of cancer related death in women worldwide, is a heterogeneous disease with diverse subtypes that have different properties and prognoses. The developing mammary gland is a highly proliferative and invasive tissue, and some of the developmental programs may be aberrantly activated to promote breast cancer progression. In the breast, luminal epithelial cells exhibit apical-basal polarity, and the failure to maintain this organizational structure, due to disruption of polarity complexes, is implicated in promoting hyperplasia and tumors. Therefore, understanding the mechanisms underlying loss of polarity will contribute to our knowledge of the early stages leading to the pathogenesis of the disease. In this review, we will discuss recent findings that support the idea that loss of apical-basal cell polarity is a crucial step in the acquisition of the malignant phenotype. Oncogene induced loss of tissue organization shares a conserved cellular mechanism with developmental process, we will further describe the role of the individual polarity complexes, the Par, Crumbs, and Scribble, to couple cell division orientation and cell growth. We will examine symmetric or asymmetric cell divisions in mammary stem cell and their contribution to the development of breast cancer subtypes and cancer stem cells. Finally, we will highlight some of the recent advances in our understanding of the molecular mechanisms by which changes in epithelial polarity programs promote invasion and metastasis through single cell and collective cell modes. J. Cell. Biochem. 117: 2215-2223, 2016. © 2016 Wiley Periodicals, Inc.

摘要

乳腺癌是全球女性癌症相关死亡的主要原因之一,是一种具有多种亚型的异质性疾病,这些亚型具有不同的特性和预后。发育中的乳腺是一种高度增殖和侵袭性的组织,一些发育程序可能会异常激活,从而促进乳腺癌的进展。在乳腺中,管腔上皮细胞呈现顶-基极性,由于极性复合体的破坏而未能维持这种组织结构,与促进增生和肿瘤形成有关。因此,了解极性丧失的潜在机制将有助于我们了解导致该疾病发病机制的早期阶段。在这篇综述中,我们将讨论最近的研究发现,这些发现支持这样一种观点,即顶-基细胞极性丧失是获得恶性表型的关键步骤。致癌基因诱导的组织组织丧失与发育过程共享一种保守的细胞机制,我们将进一步描述单个极性复合体(Par、Crumbs和Scribble)在耦合细胞分裂方向和细胞生长方面的作用。我们将研究乳腺干细胞中的对称或不对称细胞分裂及其对乳腺癌亚型和癌症干细胞发展的贡献。最后,我们将重点介绍我们在理解上皮极性程序变化通过单细胞和集体细胞模式促进侵袭和转移的分子机制方面的一些最新进展。《细胞生物化学杂志》117: 2215 - 2223, 2016。© 2016威利期刊公司。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验