2010
DOI: 10.1016/j.biopha.2010.01.018
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Deregulated expression of miR-21, miR-143 and miR-181a in non small cell lung cancer is related to clinicopathologic characteristics or patient prognosis

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Cited by 232 publications
(189 citation statements)
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“…It has been reported that miR-143 is downexpressed in colon (15), lung (16) and prostate cancer (17) and is overexpressed in hepatocarcinoma (18). Furthermore, miR-143 is involved in the regulation of MYO6 expression in prostate cancer (17); extracellular signal-regulated kinase-5 (ERK-5) is a miR-143 target in prostate cancer and miR-143 inhibits the proliferation at least in part by the inhibition of ERK-5 activity (19).…”
Section: Discussionmentioning
confidence: 99%
“…It has been reported that miR-143 is downexpressed in colon (15), lung (16) and prostate cancer (17) and is overexpressed in hepatocarcinoma (18). Furthermore, miR-143 is involved in the regulation of MYO6 expression in prostate cancer (17); extracellular signal-regulated kinase-5 (ERK-5) is a miR-143 target in prostate cancer and miR-143 inhibits the proliferation at least in part by the inhibition of ERK-5 activity (19).…”
Section: Discussionmentioning
confidence: 99%
“…The identification of microRNAs (miRNAs) has opened a new avenue for developing highly reliable diagnostic and prognostic biomarkers to facilitate the early diagnosis of NSCLC and predict the clinical outcomes of patients (3,4). At present, numerous single miRNAs, including let-7a-2 (5), miRNA-146b (6), miRNA-155 (5,6), miRNA-31 (7), miRNA-374a (8), miRNA-451 (9) and miRNA-21 (10,11) have been reported to be associated with the tumorigenesis and progression of lung cancer.…”
Section: Introductionmentioning
confidence: 99%
“…miR-181a acts as an intrinsic antigen sensitivity ''rheostat'' in T cells. Abnormally low miR-181a expression was reported in patients with acute myeloid leukemia, chronic lymphocytic leukemia, non-small cell lung cancer, adult T-cell leukemia, and glioblastoma [24][25][26][27][28]. Additionally, miR181a displays tumor suppressive effects against oral squamous cell carcinoma and glioma cells by suppressing cell proliferation [29,30].…”
Section: Introductionmentioning
confidence: 99%