miR-181a/b therapy in lung cancer: reality or myth?

被引:40
|
作者
Braicu, Cornelia [1 ]
Gulei, Diana [2 ]
Cojocneanu, Roxana [1 ]
Raduly, Lajos [1 ]
Jurj, Ancuta [1 ]
Knutsen, Erik [3 ]
Calin, George Adrian [3 ,4 ]
Berindan-Neagoe, Ioana [1 ,2 ,5 ]
机构
[1] Iuliu Hatieganu Univ Med & Pharm, Res Ctr Funct Genom Biomed & Translat Med, 23 Marinescu St, Cluj Napoca 40015, Romania
[2] Iuliu Hatieganu Univ Med & Pharm, MedFuture Res Ctr Adv Med, Cluj Napoca 40015, Romania
[3] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, 1515 Holcombe Blvd Unit 1950, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Ctr RNA Inference & Noncoding RNA, Houston, TX 77030 USA
[5] Oncol Inst Prof Dr Ion Chiricuta, Dept Funct Genom & Expt Pathol, Cluj Napoca, Romania
基金
美国国家卫生研究院;
关键词
lung cancer; miR-181a/b; therapy; BREAST-CANCER; MESENCHYMAL TRANSITION; NONCODING RNAS; MULTIDRUG-RESISTANCE; CELL-PROLIFERATION; EXPRESSION LEVELS; CERVICAL-CANCER; DOWN-REGULATION; MICRORNA; TUMOR;
D O I
10.1002/1878-0261.12420
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite substantial progress in oncology, lung cancer remains the number one malignancy in terms of both incidence and mortality rates, and there thus remains an urgent need for new therapeutic alternatives. MicroRNA (miRNA) have an important role in cancer initiation and progression due to their capacity to interfere with transcriptional signaling and regulate key cellular processes. miR-181a and miR-181b (miR-181a/b), which are located on chromosomes 1 and 9, are pathologically expressed in the tumor tissue and plasma of patients diagnosed with lung cancer. The miR-181a/b regulatory mechanisms are sophisticated and are directly related to different target genes. In recent years, an ever-increasing number of studies have focused on the biological relevance of miR-181a/b in key cellular processes. In this paper, we aim to discuss the challenging experimental data related to miR-181a/b and their potential use for the development of new therapeutic approaches in lung cancer. We will further present the ongoing issues regarding the regulation of their multiple target genes, and their potential use as biomarkers and therapeutic targets in this deadly malignancy.
引用
收藏
页码:9 / 25
页数:17
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