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头颈部癌症中的微小RNA异常:发病机制及临床意义

MicroRNA aberrances in head and neck cancer: pathogenetic and clinical significance.

作者信息

Tu Hsi-Feng, Lin Shu-Chun, Chang Kuo-Wei

机构信息

Department of Dentistry, National Yang-Ming University Hospital, Yi-Lan, Taiwan.

出版信息

Curr Opin Otolaryngol Head Neck Surg. 2013 Apr;21(2):104-11. doi: 10.1097/MOO.0b013e32835e1d6e.

Abstract

PURPOSE OF REVIEW

MicroRNAs (miRNAs) play crucial roles in modulating the neoplastic process of cancers including head and neck squamous cell carcinoma (HNSCC). miRNAs modulate pathogenesis by inhibiting target genes. Understanding how aberrant miRNAs are involved in HNSCC pathogenesis should help to validate potential clinical applications that target these entities.

RECENT FINDINGS

miR-21, miR-31, miR-504 and miR-10b are important oncogenic miRNAs that are involved in HNSCC and target tumour suppressor genes. The tumour suppressor roles of the let-7 family, the miR-99 family, miR-107, miR-133a, miR-137, miR-138 and miR-375 with respect to their targeting of oncogenes are unequivocal and have been confirmed by many studies. In addition, miR-21, let-7, miR-107, miR-138 and miR-200c seem to play complicated roles in regulating stemness or the epithelial-mesenchymal transition of tumour cells. The clinical implications of these tumour-associated miRNAs are generally in agreement with their functional roles.

SUMMARY

A number of pathways that become disregulated by aberrant miRNAs have been identified specifically for HNSCC. Analysis of these networks and their therapeutic interception might facilitate the prediction of disease status and help with the design of therapeutic trials.

摘要

综述目的

微小RNA(miRNA)在调控包括头颈部鳞状细胞癌(HNSCC)在内的癌症的肿瘤形成过程中发挥着关键作用。miRNA通过抑制靶基因来调节发病机制。了解异常miRNA如何参与HNSCC发病机制应有助于验证针对这些实体的潜在临床应用。

最新发现

miR-21、miR-31、miR-504和miR-10b是参与HNSCC并靶向肿瘤抑制基因的重要致癌miRNA。let-7家族、miR-99家族、miR-107、miR-133a、miR-137、miR-138和miR-375在靶向癌基因方面的肿瘤抑制作用是明确的,并且已得到许多研究的证实。此外,miR-21、let-7、miR-107、miR-138和miR-200c似乎在调节肿瘤细胞的干性或上皮-间质转化中发挥复杂作用。这些肿瘤相关miRNA的临床意义与其功能作用总体上是一致的。

总结

已经专门针对HNSCC确定了一些因异常miRNA而失调的途径。对这些网络及其治疗性阻断的分析可能有助于预测疾病状态并有助于设计治疗试验。

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