Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Mechanistic Insights of hsa-mir-301a Regulation by Tobacco Smoke in Lung Squamous Cell Carcinoma: Evidence From Bioinformatics Analysis. / Pustylnyak, Vladimir O.; Perevalova, Alina M.; Gulyaeva, Lyudmila F.
в: Bioinformatics and Biology Insights, Том 18, 05.12.2024, стр. 1-8.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Mechanistic Insights of hsa-mir-301a Regulation by Tobacco Smoke in Lung Squamous Cell Carcinoma: Evidence From Bioinformatics Analysis
AU - Pustylnyak, Vladimir O.
AU - Perevalova, Alina M.
AU - Gulyaeva, Lyudmila F.
N1 - The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This research was funded by RUSSIAN SCIENCE FOUNDATION (grant no. 22-15-00065).
PY - 2024/12/5
Y1 - 2024/12/5
N2 - MicroRNAs play a significant role in the development of cancers, including lung cancer. A recent study revealed that smoking, a key risk factor for lung cancer, increased the levels of hsa-mir-301a in the tumor tissues of patients with lung squamous cell carcinoma (LUSC). The aim of the current study is to investigate the mechanism by which tobacco smoke increases hsa-mir-301a levels in LUSC tumor tissues using bioinformatics analysis. Bioinformatics tools and online databases, including The Cancer Genome Atlas (TCGA), LinkedOmics, and Encyclopedia of RNA Interactomes (ENCORI), were applied in this study. Our results showed a correlation between the upregulation of hsa-mir-301a in LUSC tissues and smoking exposure. However, no correlation was discovered between patients’ smoking status and the expression level of the hsa-mir-301a host gene, SKA2, prompting us to investigate possible changes in microRNA processing under tobacco smoke exposure. In silico results using online platforms suggest that post-transcriptional processes, which involve the RNA-binding proteins DGCR8 and FUS, contribute to the elevation of mature hsa-mir-301a levels in smoking patients with LUSC. Our findings suggest that RNA-binding proteins play a key role in controlling the processing of hsa-mir-301a, indicating a complex regulation of hsa-mir-301a in the LUSC tissues of smokers.
AB - MicroRNAs play a significant role in the development of cancers, including lung cancer. A recent study revealed that smoking, a key risk factor for lung cancer, increased the levels of hsa-mir-301a in the tumor tissues of patients with lung squamous cell carcinoma (LUSC). The aim of the current study is to investigate the mechanism by which tobacco smoke increases hsa-mir-301a levels in LUSC tumor tissues using bioinformatics analysis. Bioinformatics tools and online databases, including The Cancer Genome Atlas (TCGA), LinkedOmics, and Encyclopedia of RNA Interactomes (ENCORI), were applied in this study. Our results showed a correlation between the upregulation of hsa-mir-301a in LUSC tissues and smoking exposure. However, no correlation was discovered between patients’ smoking status and the expression level of the hsa-mir-301a host gene, SKA2, prompting us to investigate possible changes in microRNA processing under tobacco smoke exposure. In silico results using online platforms suggest that post-transcriptional processes, which involve the RNA-binding proteins DGCR8 and FUS, contribute to the elevation of mature hsa-mir-301a levels in smoking patients with LUSC. Our findings suggest that RNA-binding proteins play a key role in controlling the processing of hsa-mir-301a, indicating a complex regulation of hsa-mir-301a in the LUSC tissues of smokers.
KW - DGCR8
KW - DICER1
KW - FUS
KW - lung cancer
KW - microRNA
KW - mir-301a
KW - tobacco smoke
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85210745892&origin=inward&txGid=9379484c70d5d7d939e44b0d8ad4aefd
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:001366379200001
UR - https://www.mendeley.com/catalogue/09e1f020-ec84-32a7-8ed8-d98289029556/
U2 - 10.1177/11779322241302168
DO - 10.1177/11779322241302168
M3 - Article
C2 - 39619736
VL - 18
SP - 1
EP - 8
JO - Bioinformatics and Biology Insights
JF - Bioinformatics and Biology Insights
SN - 1177-9322
ER -
ID: 61161960