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用于癌症治疗的细胞质聚腺苷酸化元件结合蛋白表达的调控

Regulation of the Expression of Cytoplasmic Polyadenylation Element Binding Proteins for the Treatment of Cancer.

作者信息

Chen Yun, Tsai Ya-Hui, Tseng Sheng-Hong

机构信息

Department of Surgery, Far Eastern Memorial Hospital, New Taipei, Taiwan, R.O.C.

Department of Chemical Engineering and Materials Science, Yuan Ze University, Taoyuan, Taiwan, R.O.C.

出版信息

Anticancer Res. 2016 Nov;36(11):5673-5680. doi: 10.21873/anticanres.11150.

Abstract

Regulated mRNA translation plays an important role in normal cellular functions and cytoplasmic polyadenylation element binding proteins (CPEBs) are the key factors that control the elongation of poly(A) tail during translation. The expression of various CPEBs has been noted to be linked to tumorigenesis, tumor growth, invasiveness and angiogenesis; however, different CPEBs appear to play diverse roles in cancer. The evidence from the literature suggests that CPEB1 and CPEB3 act more likely as tumor suppressors; in contrast, CPEB2 and CPEB4 mainly exert oncogenic effects. In addition, different CPEB subtypes may interact with each other to regulate tumorigenesis. All four CPEB mRNAs contain multiple microRNA (miRNA) binding sites, while the functions of CPEBs are regulated by various miRNAs. These results indicate that CPEBs play a significant role in tumorigenesis; therefore, manipulation of the expression of different subtypes of CPEBs might modulate the behavior of cancer cells and provide new therapeutic concepts for cancer therapy. However, more studies are required to clarify their definite role in tumor development.

摘要

受调控的mRNA翻译在正常细胞功能中起重要作用,而细胞质聚腺苷酸化元件结合蛋白(CPEBs)是翻译过程中控制聚(A)尾延长的关键因素。已注意到各种CPEBs的表达与肿瘤发生、肿瘤生长、侵袭性和血管生成有关;然而,不同的CPEBs在癌症中似乎发挥着不同的作用。文献证据表明,CPEB1和CPEB3更有可能作为肿瘤抑制因子发挥作用;相反,CPEB2和CPEB4主要发挥致癌作用。此外,不同的CPEB亚型可能相互作用以调节肿瘤发生。所有四种CPEB mRNA都包含多个微小RNA(miRNA)结合位点,而CPEBs的功能受各种miRNA调控。这些结果表明,CPEBs在肿瘤发生中起重要作用;因此,操纵不同亚型CPEBs的表达可能会调节癌细胞的行为,并为癌症治疗提供新的治疗理念。然而,需要更多的研究来阐明它们在肿瘤发展中的明确作用。

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