MicroRNA-495: a therapeutic and diagnostic tumor marker

被引:0
作者
Amirhosein Maharati
Faezeh Tolue Ghasaban
Iman Akhlaghipour
Negin Taghehchian
Amir Sadra Zangouei
Meysam Moghbeli
机构
[1] Mashhad University of Medical Sciences,Student Research Committee, Faculty of Medicine
[2] Mashhad University of Medical Sciences,Department of Medical Genetics and Molecular Medicine, School of Medicine
[3] Mashhad University of Medical Sciences,Medical Genetics Research Center
来源
Journal of Molecular Histology | 2023年 / 54卷
关键词
MicroRNA-495; Cancer; Non-invasive; Diagnosis; Prognosis; Early detection;
D O I
暂无
中图分类号
学科分类号
摘要
Therapeutic and diagnostic progresses have significantly reduced the mortality rate among cancer patients during the last decade. However, there is still a high rate of mortality among cancer patients. One of the important reasons involved in the high mortality rate is the late diagnosis in advanced tumor stages that causes the failure of therapeutic strategies in these patients. Therefore, investigating the molecular mechanisms involved in tumor progression has an important role in introducing the efficient early detection markers. MicroRNAs (miRNAs) as stable factors in body fluids are always considered as non-invasive diagnostic and prognostic markers. In the present review, we investigated the role of miR-495 in tumor progression. It has been reported that miR-495 has mainly a tumor suppressor function through the regulation of transcription factors and tyrosine kinases as well as cellular processes such as multidrug resistance, chromatin remodeling, and signaling pathways. This review can be an effective step towards introducing the miR-495 as a non-invasive diagnostic/prognostic marker as well as a suitable target in tumor therapy.
引用
收藏
页码:559 / 578
页数:19
相关论文
共 1593 条
  • [11] Andersson ER(2012)HOXA1 is overexpressed in oral squamous cell carcinomas and its expression is correlated with poor prognosis BMC Cancer 12 146-51
  • [12] Lendahl U(2012)The effects of deregulated DNA damage signalling on cancer chemotherapy response and resistance Nat Rev Cancer 12 587-1288
  • [13] Back SH(2004)Mi-2/NuRD: multiple complexes for many purposes Biochim Biophys Acta 1677 52-164
  • [14] Schröder M(2003)Tissue-specific nuclear architecture and gene expession regulated by SATB1 Nat Genet 34 42-2741
  • [15] Lee K(2006)SATB1 packages densely looped, transcriptionally active chromatin for coordinated expression of cytokine genes Nat Genet 38 1278-872
  • [16] Zhang K(2004)The functions of E (Z)/EZH2-mediated methylation of lysine 27 in histone H3 Curr Opin Genet Dev 14 155-1430
  • [17] Kaufman RJ(2011)BMI1 as a novel target for drug discovery in cancer J Cell Biochem 112 2729-55
  • [18] Bai Z(2014)MicroRNA-495 induces breast cancer cell migration by targeting JAM-A Protein Cell 5 862-8829
  • [19] Wang J(2013)The notch signaling pathway as a mediator of tumor survival Carcinogenesis 34 1420-384
  • [20] Wang T(1996)Prenylation of oncogenic human PTP(CAAX) protein tyrosine phosphatases Cancer Lett 110 49-2026