Expression levels and cotargets of miRNA1263p and miRNA1265p in lung adenocarcinoma tissues: Αn exploration with RTqPCR, microarray and bioinformatic analyses.
Oncol Rep
; 41(2): 939-953, 2019 Feb.
Article
em En
| MEDLINE
| ID: mdl-30535503
Lung adenocarcinoma (LUAD) is the most common histological subtype of lung cancer. Previous studies have found that many microRNAs (miRNAs), including miRNA1263p, may play a critical role in the development of LUAD. However, no study of LUAD has researched the synergistic effects and cotargets of both miRNA1263p and miRNA1265p. The present study used realtime quantitative polymerase chain reaction (RTqPCR) to explore the expression values of miRNA1263p and miRNA1265p in 101 LUAD and 101 normal lung tissues. Ten relevant microarray datasets were screened to further validate the expression levels of miRNA1263p and 5p in LUAD. Twelve prediction tools were employed to obtain potential targets of miRNA1263p and miRNA1265p. The results showed that both miRNA1263p and 5p were expressed significantly lower in LUAD. A significant positive correlation was also present between miRNA1263p and 5p expression in LUAD. In addition, lower expression of miRNA1263p and 5p was indicative of vascular invasion, lymph node metastasis (LNM), and a later tumor/node/metastasis (TNM) stage of LUAD. The authors obtained 167 targets of miRNA1263p and 212 targets of miRNA1265p; 44 targets were cotargets of both. Eight cotarget genes (IGF2BP1, TRPM8, DUSP4, SOX11, PLOD2, LIN28A, LIN28B and SLC7A11) were initially identified as key genes in LUAD. The results of the present study indicated that the coregulation of miRNA1263p and miRNA1265p plays a key role in the development of LUAD, which also suggests a failproof mode between miRNA3p and miRNA1265p.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Biomarcadores Tumorais
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Regulação Neoplásica da Expressão Gênica
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MicroRNAs
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Adenocarcinoma de Pulmão
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Neoplasias Pulmonares
Tipo de estudo:
Diagnostic_studies
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Prognostic_studies
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Systematic_reviews
Limite:
Humans
Idioma:
En
Ano de publicação:
2019
Tipo de documento:
Article