Department of Biochemistry and Medical Biotechnology, University of Naples "Federico II". Via S. Pansini 5, 80131 Napoli, Italy.
Curr Med Chem. 2011;18(35):5424-9. doi: 10.2174/092986711798194333.
FK506 binding protein 51 (FKBP51) is an immunophilin physiologically expressed in lymphocytes. Very recently, aberrant expression of this protein was found in melanoma; FKBP51 expression correlates with melanoma aggressiveness and is maximal in metastatic lesions. FKBP51 promotes NF-κB activation and is involved in the resistance to genotoxic agents, including anthracyclines and ionizing radiation. FKBP51 is a cochaperone with peptidyl-prolyl isomerase activity that regulates several biological processes through protein-protein interaction. There is increasing evidence that FKBP51 hyperexpression is associated with cancer and this protein has a relevant role in sustaining cell growth, malignancy, and resistance to therapy. There is also evidence that FKBP ligands are potent anticancer agents, in addition to their immunosuppressant activity. In particular, rapamycin and its analogs have shown antitumor activity across a variety of human cancers in clinical trials. Although, classically, rapamycin actions are ascribed to inhibition of mTOR, recent studies indicate FKBP51 is also an important molecular determinant of the drug's anticancer activity. The aim of this article is to review the functions of FKBP51, especially in view of the recent findings that this protein is a potential oncogene when deregulated and a candidate target for signaling therapies against cancer.
FK506 结合蛋白 51(FKBP51)是一种在淋巴细胞中生理性表达的免疫亲和素。最近,人们发现这种蛋白在黑色素瘤中异常表达;FKBP51 的表达与黑色素瘤的侵袭性相关,在转移性病变中表达最强。FKBP51 促进 NF-κB 的激活,并参与对包括蒽环类药物和电离辐射在内的遗传毒性药物的耐药性。FKBP51 是一种具有肽基脯氨酰顺反异构酶活性的共伴侣,通过蛋白质-蛋白质相互作用调节多种生物学过程。越来越多的证据表明,FKBP51 的过度表达与癌症有关,并且这种蛋白质在维持细胞生长、恶性肿瘤和对治疗的耐药性方面具有重要作用。还有证据表明,FKBP 配体除了具有免疫抑制活性外,还是有效的抗癌药物。特别是,雷帕霉素及其类似物在临床试验中显示出对多种人类癌症的抗肿瘤活性。尽管雷帕霉素的作用经典上归因于 mTOR 的抑制,但最近的研究表明 FKBP51 也是该药物抗肿瘤活性的一个重要分子决定因素。本文的目的是综述 FKBP51 的功能,特别是鉴于最近的发现,当这种蛋白失调时,它是一种潜在的癌基因,也是针对癌症信号转导治疗的候选靶点。