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首页> 外文期刊>Critical reviews in oncology/hematology >Embryological signaling pathways in Barrett's metaplasia development and malignant transformation; Mechanisms and therapeutic opportunities
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Embryological signaling pathways in Barrett's metaplasia development and malignant transformation; Mechanisms and therapeutic opportunities

机译:Barrett上皮化生和恶性转化中的胚胎信号通路;机制和治疗机会

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摘要

Barrett's metaplasia of the esophagus (BE) is the precursor lesion of esophageal adenocarcinoma (EAC), a deadly disease with a 5-year overall survival of less than 20%. The molecular mechanisms of BE development and its transformation to EAC are poorly understood and current surveillance and treatment strategies are of limited efficacy. Increasing evidence suggests that aberrant signaling through pathways active in the embryological development of the esophagus contributes to BE development and progression to EAC. We discuss the role that the Bone morphogenetic protein, Hedgehog, Wingless-Type MMTV Integration Site Family (WNT) and Retinoic acid signaling pathways play during embryological development of the esophagus and their contribution to BE development and malignant transformation. Modulation of these pathways provides new therapeutic opportunities. By integrating findings in developmental biology with those from translational research and clinical trials, this review provides a platform for future studies aimed at improving current management of BE and EAC.
机译:食管的巴雷特化生(BE)是食管腺癌(EAC)的前体病变,这是一种致命疾病,其5年总生存率不到20%。对BE发生及其转化为EAC的分子机制了解甚少,目前的监视和治疗策略疗效有限。越来越多的证据表明,通过食道胚胎发育中活跃的途径引起的异常信号有助于BE的发展和向EAC的发展。我们讨论了食管胚胎发育过程中骨形态发生蛋白,刺猬,无翅型MMTV整合位点家族(WNT)和视黄酸信号通路的作用以及它们对BE发育和恶性转化的贡献。这些途径的调节提供了新的治疗机会。通过将发育生物学的发现与转化研究和临床试验的发现相结合,本综述为将来的研究提供了一个平台,旨在改善目前对BE和EAC的管理。

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