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卵巢癌的免疫发病机制。

Immunopathogenesis of ovarian cancer.

机构信息

Department of Gynecologic Oncology, University of Texas M. D. Anderson Cancer Canter, Houston TX, USA.

出版信息

Minerva Med. 2009 Oct;100(5):357-70.

Abstract

Immune cells in the ovarian stromal microenvironment play an important role in ovarian tumorigenesis. Up-regulation of immune cell-derived mediators during ovulation may generate a proinflammatory niche, which may subsequently induce transformation of normal ovarian epithelial cells or endometriotic cells in the ovary. Once transformed ovarian epithelial cells develop, an immunoediting process occurs in which immune cells and their mediators dictate the development and progression of ovarian tumors. Tumor cells also develop several mechanisms to evade anti-tumor immunity by developing an immunosuppressive microenvironment. The differences in the population of immune cells infiltrating into ovarian tumor tissues are associated with differences in clinical outcomes. The underlying molecular mechanisms of the association begin to unravel with the development of microdissection techniques, high throughput technologies, in vitro functional assays, and in vivo mouse modeling. A better understanding of the complex relationship between ovarian tumor cells and the associated immune cells will allow us to develop novel immunologic strategies for ovarian cancer prevention and treatment.

摘要

卵巢基质微环境中的免疫细胞在卵巢肿瘤发生中起着重要作用。排卵期间免疫细胞来源的介质的上调可能会产生一个促炎的微环境,随后可能会诱导正常卵巢上皮细胞或卵巢内的子宫内膜异位细胞发生转化。一旦转化的卵巢上皮细胞发生发展,就会发生免疫编辑过程,其中免疫细胞及其介质决定卵巢肿瘤的发生和进展。肿瘤细胞还通过形成免疫抑制性微环境来发展几种逃避抗肿瘤免疫的机制。浸润到卵巢肿瘤组织中的免疫细胞的群体差异与临床结局的差异有关。随着显微解剖技术、高通量技术、体外功能测定和体内小鼠模型的发展,与这种关联相关的潜在分子机制开始被揭示。更好地理解卵巢肿瘤细胞与相关免疫细胞之间的复杂关系,将使我们能够开发用于卵巢癌预防和治疗的新型免疫策略。

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