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使黑色素瘤扩散的FKBP51的分子机制

Molecular Aspects of FKBP51 that Enable Melanoma Dissemination.

作者信息

D'Angelillo Anna, Staibano Stefania, Russo Michele, Romano Maria F, Romano Simona

机构信息

Department of Molecular Medicine and Medical Biotechnologies, Federico II University, Via Pansini, 5. 80131. Naples, Italy.

出版信息

Curr Mol Pharmacol. 2015;9(2):141-7. doi: 10.2174/1874467208666150519115242.

Abstract

FKBP51 (FKBP5 Official Symbol) is large molecular weight member of the FK506 binding protein family, a subfamily of the immunophilin proteins. FKBP51 exerts multiple biological functions in the cell, including modulation of steroid hormone response, immune regulation, cell proliferation, regulation of pAkt levels and control of NF-κB activation. Several lines of evidence support a role for this protein in cancer biology, especially in resistance to chemo- and radio-therapy. Recent research studies highlighted functions of FKBP51 in promoting the epithelial to mesenchymal transition (EMT) transdifferentiation program in melanoma. This process, which is classically regulated by Transforming Growth Factor (TGF)-β, enables cancer cells to disseminate from primary tumors and spread to distant locations, acquiring resistance to therapy and self-renewal capability. This last, in turn, is crucial to their subsequent expansion at sites of dissemination. The aim of the present article is to review recent literature data that involve FKBP51 in the mechanisms that switch the TGF-β from a tumor suppressor to a pro-metastatic invader.

摘要

FKBP51(FKBP5官方符号)是FK506结合蛋白家族的大分子成员,属于亲免素蛋白亚家族。FKBP51在细胞中发挥多种生物学功能,包括调节类固醇激素反应、免疫调节、细胞增殖、pAkt水平调控以及NF-κB激活的控制。多项证据支持该蛋白在癌症生物学中的作用,尤其是在化疗和放疗抗性方面。最近的研究突出了FKBP51在促进黑色素瘤上皮-间质转化(EMT)转分化程序中的功能。这一过程经典地由转化生长因子(TGF)-β调节,使癌细胞能够从原发性肿瘤扩散并转移到远处,获得对治疗的抗性和自我更新能力。而后者对于它们随后在转移部位的扩张至关重要。本文的目的是综述最近的文献数据,这些数据涉及FKBP51在将TGF-β从肿瘤抑制因子转变为促转移侵袭因子的机制中的作用。

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