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受体酪氨酸激酶与血吸虫生殖:化疗新靶点。

Receptor tyrosine kinases and schistosome reproduction: new targets for chemotherapy.

机构信息

Center for Infection and Immunity of Lille, INSERM U1019, CNRS-UMR 8204, Institut Pasteur de Lille, University Lille Nord de France Lille Cedex, France.

Biomedical Centre for Research Seltersberg, Institute of Parasitology, Justus-Liebig-University Giessen Giessen, Germany.

出版信息

Front Genet. 2014 Jul 18;5:238. doi: 10.3389/fgene.2014.00238. eCollection 2014.

Abstract

Schistosome parasites still represent a serious public health concern and a major economic problem in developing countries. Pathology of schistosomiasis is mainly due to massive egg production by these parasites and to inflammatory responses raised against the eggs which are trapped in host tissues. Tyrosine kinases (TKs) are key molecules that control cell differentiation and proliferation and they already represent important targets in cancer therapy. During recent years, it has been shown that receptor tyrosine kinases (RTK) signaling was active in reproductive organs and that it could regulate sexual maturation of schistosomes and egg production. This opens interesting perspectives for the control of transmission and pathogenesis of schistosomiasis based on new therapies targeting schistosome RTKs. This review relates the numerous data showing the major roles of kinase signaling in schistosome reproduction. It describes the conserved and particular features of schistosome RTKs, their implication in gametogenesis and reproduction processes and summarizes recent works indicating that RTKs and their signaling partners are interesting chemotherapeutical targets in new programs of control.

摘要

血吸虫寄生虫仍然是发展中国家严重的公共卫生问题和重大经济问题。血吸虫病的病理学主要是由于这些寄生虫大量产卵和对被困在宿主组织中的卵的炎症反应引起的。酪氨酸激酶(TKs)是控制细胞分化和增殖的关键分子,它们已经成为癌症治疗的重要靶点。近年来,已经表明受体酪氨酸激酶(RTK)信号在生殖器官中活跃,并可以调节血吸虫的性成熟和产卵。这为基于针对血吸虫 RTKs 的新疗法来控制血吸虫病的传播和发病机制开辟了有趣的前景。这篇综述涉及了大量数据,这些数据表明激酶信号在血吸虫繁殖中的重要作用。它描述了血吸虫 RTKs 的保守和特殊特征,它们在配子发生和繁殖过程中的作用,并总结了最近的工作,表明 RTKs 及其信号伙伴是新的控制计划中有趣的化学治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/639d/4102852/c47caf1f22a6/fgene-05-00238-g001.jpg

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