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首页> 外文期刊>Current opinion in clinical nutrition and metabolic care >Fn14: a new player in cancer-induced cachexia
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Fn14: a new player in cancer-induced cachexia

机译:Fn14:癌症诱发恶病质的新参与者

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Purpose of reviewAlthough cancer cachexia is a very significant condition that is present in up to 80% of cancer cases, the cause of the condition has remained a puzzle. Cancer cachexia is a condition which is mainly characterised by muscle wasting, mobilization of fat reserves, and overall metabolic disturbance. This review aims to highlight some of the recent findings in cancer cachexia research.Recent researchIt has been recently demonstrated that the expression of a single receptor, fibroblast growth factor-inducible 14, on a tumour can initiate cachexia and that this can be completely ablated by treatment with an antibody against this receptor. Also recently described was the role of parathyroid hormone receptor-binding proteins in causing cachexia through a mechanism where white adipose tissue is replaced with brown adipose tissue. In parallel, work done in drosophila suggests that the impaired insulin signalling is a direct cause of cancer cachexia through the release of an insulin growth factor binding protein that inhibits insulin and insulin-like growth factor 1 signalling.SummarySuccessful therapies are urgently needed to combat cancer cachexia in the clinic. Recent research is making progress toward discovering the underlying molecular causes of the condition, which could lead to new therapeutic approaches and in the future contribute to more positive clinical outcomes for cancer sufferers.
机译:回顾的目的尽管癌症恶病质是一种非常重要的疾病,在多达80%的癌症病例中都存在,但造成这种疾病的原因仍然令人困惑。癌症恶病质是主要以肌肉消耗,脂肪储备的动员和整体代谢紊乱为特征的病症。这篇综述旨在突出癌症恶病质研究中的一些最新发现。最近的研究表明,肿瘤上单一受体(成纤维细胞生长因子诱导型14)的表达可以引发恶病质,并且可以通过以下方法彻底消除恶病质:用针对该受体的抗体进行治疗。最近还描述了甲状旁腺激素受体结合蛋白在通过白色脂肪组织被棕色脂肪组织代替的机制引起恶病质中的作用。同时,在果蝇中进行的工作表明,胰岛素信号传导受损是通过释放抑制胰岛素和类胰岛素生长因子1信号传导的胰岛素生长因子结合蛋白而导致的癌症恶病质的直接原因。迫切需要成功的疗法来对抗癌症恶病质在诊所。最近的研究正在朝发现该病的潜在分子原因方面取得进展,这可能会导致新的治疗方法,并在将来为癌症患者带来更积极的临床结果。

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