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年轻和衰老的乳腺上皮细胞中的细胞外信号及其与年龄相关的乳腺癌发展的可能联系。

Extracellular signals in young and aging breast epithelial cells and possible connections to age-associated breast cancer development.

机构信息

Department of Gynecology, Biochemistry and Tumor Biology Lab (OE 6411), Medical School Hannover, Germany.

出版信息

Mech Ageing Dev. 2011 May;132(5):213-9. doi: 10.1016/j.mad.2011.04.002. Epub 2011 Apr 9.

Abstract

Aging of human breast tissue is accompanied by certain structural and functional variations and several studies suggest a possible contribution of these changes to an aging-related breast cancer development. At the cellular level, aging of human mammary epithelial cells is associated with significant morphological and functional alterations such as an increased cell size and a reduced proliferation. Cellular senescence of HMEC cannot be explained by a single mechanism but represents an interaction of numerous extra- and intracellular events and the complexity of such orchestrating pathways is still hardly understood. Besides the contribution of reactive oxygen species and telomere dysfunction to aging, it is the aim of this mini-review, to compare distinct changes to extracellular signals by certain matrix metalloproteinases including MMP-7 and associated growth factor pathways mediated by HB-EGF activation in young and aging HMEC. Such changes can alter hormone receptor levels within aged HMEC, induce tissue fibrosis and promote epithelial-to-mesenchymal transition as a potential prerequisite for breast cancer development. Moreover, an accumulation of aging cells during the normal life span of the breast tissue may also substantially effect and interact with adjacent neighboring populations in the local microenvironment to provide optimized growth conditions which would also support neoplastic cells.

摘要

人类乳房组织的老化伴随着某些结构和功能的变化,有几项研究表明,这些变化可能对与衰老相关的乳腺癌的发展有一定的贡献。在细胞水平上,人乳腺上皮细胞的老化与显著的形态和功能改变相关,例如细胞体积增大和增殖减少。HMEC 的细胞衰老不能用单一机制来解释,而是代表了众多细胞内外事件的相互作用,而这种协调途径的复杂性仍难以理解。除了活性氧和端粒功能障碍对衰老的贡献外,本综述的目的还在于比较年轻和老化的 HMEC 中某些基质金属蛋白酶(包括 MMP-7)和相关生长因子途径通过 HB-EGF 激活对细胞外信号的不同变化。这些变化可以改变老化的 HMEC 中的激素受体水平,诱导组织纤维化,并促进上皮-间充质转化,作为乳腺癌发展的潜在前提。此外,在乳腺组织的正常寿命期间,衰老细胞的积累也可能对局部微环境中相邻的邻近细胞群体产生实质性影响,并相互作用,为肿瘤细胞提供优化的生长条件。

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