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产后乳腺退化的研究揭示了新的促转移机制。

Studies of postpartum mammary gland involution reveal novel pro-metastatic mechanisms.

作者信息

Wallace Taylor R, Tarullo Sarah E, Crump Lyndsey S, Lyons Traci R

机构信息

Department of Medicine, Division of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.

Young Women's Breast Cancer Translational Program, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.

出版信息

J Cancer Metastasis Treat. 2019;5. doi: 10.20517/2394-4722.2019.01. Epub 2019 Feb 19.

Abstract

Postpartum involution is the process by which the lactating mammary gland returns to the pre-pregnant state after weaning. Expression of tumor-promotional collagen, upregulation of matrix metalloproteinases, infiltration of M2 macrophages, and remodeling of blood and lymphatic vasculature are all characteristics shared by the involuting mammary gland and breast tumor microenvironment. The tumor promotional nature of the involuting mammary gland is perhaps best evidenced by cases of postpartum breast cancer (PPBC), or those cases diagnosed within 10 years of most recent childbirth. Women with PPBC experience more aggressive disease and higher risk of metastasis than nulliparous patients and those diagnosed outside the postpartum window. Semaphorin 7a (SEMA7A), cyclooxygenase-2 (COX-2), and collagen are all expressed in the involuting mammary gland and, together, predict for decreased metastasis free survival in breast cancer. Studies investigating the role of these proteins in involution have been important for understanding their contributions to PPBC. Postpartum involution thus represents a valuable model for the identification of novel molecular drivers of PPBC and classical cancer hallmarks. In this review, we will highlight the similarities between involution and cancer in the mammary gland, and further define the contribution of SEMA7A/COX-2/collagen interplay to postpartum involution and breast tumor progression and metastasis.

摘要

产后复旧是指哺乳期乳腺在断奶后恢复到孕前状态的过程。促肿瘤胶原蛋白的表达、基质金属蛋白酶的上调、M2巨噬细胞的浸润以及血液和淋巴管系统的重塑,都是复旧期乳腺和乳腺肿瘤微环境共有的特征。产后乳腺癌(PPBC)病例,即那些在最近一次分娩后10年内被诊断出的病例,或许最能证明复旧期乳腺的促肿瘤性质。与未生育患者以及在产后窗口期外被诊断出的患者相比,PPBC女性的疾病侵袭性更强,转移风险更高。信号素7a(SEMA7A)、环氧合酶-2(COX-2)和胶原蛋白在复旧期乳腺中均有表达,它们共同预示着乳腺癌患者无转移生存期的缩短。研究这些蛋白质在复旧过程中的作用,对于理解它们对PPBC的影响具有重要意义。因此,产后复旧是识别PPBC新型分子驱动因素和经典癌症特征的宝贵模型。在这篇综述中,我们将重点介绍乳腺复旧与癌症之间的相似之处,并进一步明确SEMA7A/COX-2/胶原蛋白相互作用对产后复旧以及乳腺肿瘤进展和转移的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/217b/6400586/01ebc964ea5e/nihms-1013803-f0001.jpg

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