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Pivotal role of microRNA-138 in human cancers.
Yeh, Margaret; Oh, Christina S; Yoo, Ji Young; Kaur, Balveen; Lee, Tae Jin.
Afiliação
  • Yeh M; Department of Neurosurgery, University of Texas Health Science Center at Houston, McGovern Medical School Houston, TX 77030, USA.
  • Oh CS; Biochemistry and Cell Biology, Department of Biosciences, Rice University Houston, TX 77030, USA.
  • Yoo JY; Department of Neurosurgery, University of Texas Health Science Center at Houston, McGovern Medical School Houston, TX 77030, USA.
  • Kaur B; Department of Neurosurgery, University of Texas Health Science Center at Houston, McGovern Medical School Houston, TX 77030, USA.
  • Lee TJ; Department of Neurosurgery, University of Texas Health Science Center at Houston, McGovern Medical School Houston, TX 77030, USA.
Am J Cancer Res ; 9(6): 1118-1126, 2019.
Article em En | MEDLINE | ID: mdl-31285946
ABSTRACT
Aberrant expression of certain microRNAs (miRNAs) has been implicated in cancers as a promising druggable target due to the fact that a modulation of the deregulated single miRNA seems to revert the therapeutically unfavorable gene expressions in cancer cell by targeting multiple genes. Global miRNA profiling from a number of patient cohorts in various type of human cancers has identified miR-138 as a signature of tumor suppressor that are down-regulated in most types of human cancer. As a tumor suppressor, miR-138 can inhibit oncogenic proteins by directly bind to their mRNAs. However, in rare cases of cancer stem cell population from glioblastoma, miR-138 seems to be down-regulated and plays an oncogenic function. This review will summarize accumulating evidence that has shown the expression and functional role of miR-138 in various human cancers with its target genes and pathways in a hope to find a better therapeutic option to treat human cancers.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article