MicroRNA-135b作为癌症的治疗靶点

Ching-Wen Lin, T. Hong, Pan‐Chyr Yang
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引用次数: 4

摘要

MicroRNAs (miRNAs)是一种小的非编码rna,可以通过rna诱导的沉默复合体(RISC)介导的抑制在转录后水平负调控基因表达。由于靶序列的种子结合区不完善且较短,因此mirna具有多靶点的能力,能够调节广泛的细胞功能和信号传导。大量研究表明,mirna失调与癌症进展密切相关。此外,全基因组筛选表明,mirna的表达谱可以作为癌症患者早期诊断、患者预后分层和预测治疗效率的生物标志物。因此,寻找和剖析癌症相关miRNA的详细机制可能为癌症靶向治疗提供新的途径。这篇综述讨论了目前提出的miR-135b参与癌症进展和组织分化的机制,这两者被认为是功能等同的。我们还研究了miR-135b的调控网络,以进一步阐明miR-135b的潜在致癌作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MicroRNA-135b as therapeutic target in cancers
MicroRNAs (miRNAs) are small non-coding RNAs that can negatively regulate gene expression at the post-transcriptional level through the RNA-induced silencing complex (RISC)-mediated inhibition. Because of the imperfect and short seed-binding region of the target sequences, miRNAs hold capacity for multi-targeting and are able to regulate a wide range of cellular functions and signaling. Numerous researches have revealed that dysregulated miRNAs are closely associated with cancer progression. Moreover, genome-wide screening shows that the expression profile of miRNAs can serve as biomarkers for early diagnosis, stratifying patient outcome, and predicting treatment efficiency for cancer patients. Hence, seeking and dissecting the detailed mechanisms of cancer-associated miRNA may provide a new avenue for cancer targeting therapy. This review discussed the current proposed mechanisms of miR-135b involvement in cancer progression and tissue differentiation, both of which are considered as functional equivalents. The regulatory network of miR-135b are also addressed to further clarify the potential oncogenic role of miR-135b.
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