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Prostate-associated gene 4 (PAGE4), an intrinsically disordered cancer/testis antigen, is a novel therapeutic target for prostate cancer

机译:前列腺相关基因4(PAGE4),一种固有的癌症/睾丸抗原紊乱,是前列腺癌的新型治疗靶标

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摘要

Prostate-associated gene 4 (PAGE4) is a remarkably prostate-specific Cancer/Testis Antigen that is highly upregulated in the human fetal prostate and its diseased states but not in the adult normal gland. PAGE4 is an intrinsically disordered protein (IDP) that functions as a stress-response protein to suppress reactive oxygen species as well as prevent DNA damage. In addition, PAGE4 is also a transcriptional regulator that potentiates transactivation by the oncogene c-Jun. c-Jun forms the AP-1 complex by heterodimerizing with members of the Fos family and plays an important role in the development and pathology of the prostate gland, underscoring the importance of the PAGE4/c-Jun interaction. HIPK1, also a component of the stress-response pathway, phosphorylates PAGE4 at T51 which is critical for its transcriptional activity. Phosphorylation induces conformational and dynamic switching in the PAGE4 ensemble leading to a new cellular function. Finally, bioinformatics evidence suggests that the PAGE4 mRNA could be alternatively spliced resulting in four potential isoforms of the polypeptide alluding to the possibility of a range of conformational ensembles with latent functions. Considered together, the data suggest that PAGE4 may represent the first molecular link between stress and prostate cancer (PCa). Thus, pharmacologically targeting PAGE4 may be a novel opportunity for treating and managing patients with PCa, especially patients with low-risk disease.
机译:前列腺相关基因4(PAGE4)是一种前列腺特异性癌/睾丸抗原,在人类胎儿前列腺及其患病状态中高度上调,但在成年正常腺体中却没有。 PAGE4是一种内在无序的蛋白(IDP),它起着应激反应蛋白的作用,以抑制活性氧并防止DNA损伤。此外,PAGE4还是一种转录调节剂,可增强癌基因c-Jun的反式激活。 c-Jun通过与Fos家族成员异源二聚形成AP-1复合物,并在前列腺的发育和病理中起重要作用,从而强调了PAGE4 / c-Jun相互作用的重要性。 HIPK1,也是应激反应途径的一个组成部分,在T51磷酸化PAGE4,这对其转录活性至关重要。磷酸化诱导PAGE4集合中的构象和动态转换,从而导致新的细胞功能。最后,生物信息学证据表明,可以交替剪接PAGE4 mRNA,从而产生该多肽的四种潜在同工型,这暗示着一系列具有潜在功能的构象集合的可能性。综合考虑,数据表明PAGE4可能代表压力与前列腺癌(PCa)之间的第一个分子联系。因此,药理学上靶向PAGE4可能是治疗和管理PCa患者,尤其是低危疾病患者的新机会。

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