Dysregulation of autophagy-associated microRNAs in condyloma acuminatum.


Journal

Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
ISSN: 1567-7257
Titre abrégé: Infect Genet Evol
Pays: Netherlands
ID NLM: 101084138

Informations de publication

Date de publication:
09 2021
Historique:
received: 13 10 2020
revised: 06 04 2021
accepted: 18 04 2021
pubmed: 28 4 2021
medline: 19 1 2022
entrez: 27 4 2021
Statut: ppublish

Résumé

Condyloma acuminatum, which is caused by low-risk human papillomavirus (lrHPV) infection, is one of the most common sexually transmitted diseases. Autophagy is thought to be associated with condyloma acuminatum, but how the autophagy process is regulated remains unclear. MicroRNAs (miRNAs) are important regulators of gene transcription that play a central role in many biological processes, including autophagy and viral infection. This study was designed to identify autophagy-related miRNAs and their targets in condyloma acuminatum and to validate their expression. The levels of the autophagy proteins microtubule-associated protein 1 light chain 3 (LC3) and P62/SQSTM1 (P62) were abnormally increased in the local lesion tissue of condyloma acuminatum patients compared with healthy controls. MiRNAs and their target mRNAs in condyloma acuminatum patients were analyzed by bioinformatics. Eighty-one differentially expressed miRNAs were identified, of which 56 were downregulated and 25 were upregulated. Two of the differentially expressed miRNAs associated with autophagy, miRNA-30a-5p and miRNA-514a-3p, were analyzed further, and their target genes were identified as autophagy-related protein (Atg) 5 and Atg12 and Atg3 and Atg12, respectively. The expression levels of miRNA-30a-5p and miRNA-514a-3p were decreased and those of Atg5, Atg12 and Atg3 were increased in condyloma acuminatum patients compared with healthy controls. In addition, miRNA-30a-5p and miRNA-514a-3p expression correlated with the proliferation index Ki-67 in condyloma acuminatum. Taken together, our results suggest that the changes in autophagy levels in patients with condyloma acuminatum may be related to the changes in miRNA-30a-5p and miRNA-514a-3p expression. This study provides a theoretical basis for identifying new mechanisms that link miRNAs, HPV infection and host autophagy in vivo.

Identifiants

pubmed: 33905885
pii: S1567-1348(21)00175-1
doi: 10.1016/j.meegid.2021.104878
pii:
doi:

Substances chimiques

MicroRNAs 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

104878

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Auteurs

Shi Wu (S)

Department of Dermatology, The First Affiliated Hospital of Jinan University, Jinan University, Guangzhou 510630, China; Dermatology Institute of Jinan University, Jinan University, Guangzhou 510630, China.

Dan Lu (D)

Department of Neurology and Stroke Center, The First Affiliated Hospital of Jinan University, Jinan University, Guangzhou 510630, China; Clinical Neuroscience Institute of Jinan University, Jinan University, Guangzhou 510630, China.

Xinkai Zheng (X)

Department of Dermatology, The First Affiliated Hospital of Jinan University, Jinan University, Guangzhou 510630, China; Dermatology Institute of Jinan University, Jinan University, Guangzhou 510630, China.

Jin Xu (J)

Department of Dermatology, The First Affiliated Hospital of Jinan University, Jinan University, Guangzhou 510630, China; Dermatology Institute of Jinan University, Jinan University, Guangzhou 510630, China.

Zhen Li (Z)

Department of Dermatology, The First Affiliated Hospital of Jinan University, Jinan University, Guangzhou 510630, China; Department of Laser Cosmetology, The fifth people's hospital of Hainan Province, Haikou 570100, China.

Liehua Deng (L)

Department of Dermatology, The First Affiliated Hospital of Jinan University, Jinan University, Guangzhou 510630, China; Dermatology Institute of Jinan University, Jinan University, Guangzhou 510630, China. Electronic address: liehuadeng@126.com.

Yunfeng Hu (Y)

Department of Dermatology, The First Affiliated Hospital of Jinan University, Jinan University, Guangzhou 510630, China; Dermatology Institute of Jinan University, Jinan University, Guangzhou 510630, China. Electronic address: huyunfeng@jnu.edu.cn.

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