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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >CtBP2 could promote prostate cancer cell proliferation through c-Myc signaling
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CtBP2 could promote prostate cancer cell proliferation through c-Myc signaling

机译:CtBP2可通过c-Myc信号传导促进前列腺癌细胞的增殖

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摘要

C-terminal binding protein-2 (CtBP2) is a CtBP-family member which plays a significant role in tumor initiation, progression and response to therapy. However, little has been known about the potential oncobiological role of CtBP2 and its mechanism in human prostate cancer. In this study, we observed the overexpression of CtBP2 in prostate cancer and demonstrated that its expression was closely correlated with several malignant behaviors, e.g., increased serum PSA level, advanced tumor stage (T3), higher Gleason scores and poor outcome. Furthermore, downregulation of CtBP2 expression in prostate cancer PC3 cells could markedly inhibit their proliferation by inducing apoptosis in vitro. Additionally, CtBP2 inhibition could decrease the level of c-Myc and its direct transcriptional target, HSPC111. Taken together, our investigations demonstrated that low-expression of CtBP2 could highly inhibit proliferation of prostate cancer by c-Myc induced signaling, suggesting that targeting CtBP2 may yield a viable anti-tumor strategy by restraining tumor progression in prostate cancer.
机译:C-末端结合蛋白2(CtBP2)是CtBP家族成员,在肿瘤的发生,发展和对治疗的反应中起重要作用。然而,关于CtBP2在人类前列腺癌中的潜在的生物学作用及其机制,人们知之甚少。在这项研究中,我们观察到CtBP2在前列腺癌中的过度表达,并证明其表达与多种恶性行为密切相关,例如,血清PSA水平升高,肿瘤分期(T3)升高,格里森评分较高和不良预后。此外,前列腺癌PC3细胞中CtBP2表达的下调可通过诱导体外细胞凋亡显着抑制其增殖。此外,CtBP2抑制可以降低c-Myc及其直接转录靶标HSPC111的水平。综上所述,我们的研究表明,低表达的CtBP2可以通过c-Myc诱导的信号传导高度抑制前列腺癌的增殖,表明靶向CtBP2可以通过抑制前列腺癌的肿瘤进展而产生可行的抗肿瘤策略。

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