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Differential microRNA expression in aristolochic acid-induced upper urothelial tract cancers ex vivo

Aristolochic acid (AA) is a carcinogenic, mutagenic and nephrotoxic compound commonly isolated from members of the plant family of Aristolochiaceae (such as Aristolochia and Asarum) and used in Chinese herbal medicine. Use of AA and AA-containing plants causes chronic kidney disease (CKD) and upper...

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Autores principales: TAO, LE, ZENG, YIGANG, WANG, JUN, LIU, ZHIHONG, SHEN, BING, GE, JIFU, LIU, YONG, GUO, YIFENG, QIU, JIANXIN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626193/
https://www.ncbi.nlm.nih.gov/pubmed/26397152
http://dx.doi.org/10.3892/mmr.2015.4330
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author TAO, LE
ZENG, YIGANG
WANG, JUN
LIU, ZHIHONG
SHEN, BING
GE, JIFU
LIU, YONG
GUO, YIFENG
QIU, JIANXIN
author_facet TAO, LE
ZENG, YIGANG
WANG, JUN
LIU, ZHIHONG
SHEN, BING
GE, JIFU
LIU, YONG
GUO, YIFENG
QIU, JIANXIN
author_sort TAO, LE
collection PubMed
description Aristolochic acid (AA) is a carcinogenic, mutagenic and nephrotoxic compound commonly isolated from members of the plant family of Aristolochiaceae (such as Aristolochia and Asarum) and used in Chinese herbal medicine. Use of AA and AA-containing plants causes chronic kidney disease (CKD) and upper urinary tract carcinoma (UUC); however, the underlying mechanism remains to be defined. miRNAs regulate a number of biological processes, including cell proliferation, differentiation and metabolism. This study explored differentially expressed miRNAs between AA-induced upper urothelial tract cancer (AAN-UUC) and non-AAN-UUC tissues. Patients with AAN-UUC and non-AAN-UUC (n=20/group) were recruited in the present study. Five tissue samples from each group were used for miRNA microarray profiling and the rest of the tissue samples were subjected to reverse transcription-quantitative polymerase chain reaction analysis including seven selected miRNAs for confirmation. A total of 29 miRNAs were differentially expressed between AAN-UUC and non-AAN-UUC tissues (P<0.05). TargenScan and Gene ontology analyses predicted the functions and targeted genes of these differentially expressed miRNAs, i.e. Akt3, FGFR3, PSEN1, VEGFa and AR. Subsequently, expression of the selected differentially expressed miRNAs (Hsa-miR-4795-5p, Hsa-miR-488, Hsa-miR-4784, Hsa-miR-330, Hsa-miR-3916, Hsa-miR-4274 and Hsa-miR-181c) was validated in another set of tissue samples. A total of 29 miRNAs were identified to be differentially expressed between AAN-UUC and non-AAN-UUC tissues and these miRNA target genes in FGFR3 and Akt pathways, which regulate cell growth and tumor progression, respectively.
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spelling pubmed-46261932016-02-23 Differential microRNA expression in aristolochic acid-induced upper urothelial tract cancers ex vivo TAO, LE ZENG, YIGANG WANG, JUN LIU, ZHIHONG SHEN, BING GE, JIFU LIU, YONG GUO, YIFENG QIU, JIANXIN Mol Med Rep Articles Aristolochic acid (AA) is a carcinogenic, mutagenic and nephrotoxic compound commonly isolated from members of the plant family of Aristolochiaceae (such as Aristolochia and Asarum) and used in Chinese herbal medicine. Use of AA and AA-containing plants causes chronic kidney disease (CKD) and upper urinary tract carcinoma (UUC); however, the underlying mechanism remains to be defined. miRNAs regulate a number of biological processes, including cell proliferation, differentiation and metabolism. This study explored differentially expressed miRNAs between AA-induced upper urothelial tract cancer (AAN-UUC) and non-AAN-UUC tissues. Patients with AAN-UUC and non-AAN-UUC (n=20/group) were recruited in the present study. Five tissue samples from each group were used for miRNA microarray profiling and the rest of the tissue samples were subjected to reverse transcription-quantitative polymerase chain reaction analysis including seven selected miRNAs for confirmation. A total of 29 miRNAs were differentially expressed between AAN-UUC and non-AAN-UUC tissues (P<0.05). TargenScan and Gene ontology analyses predicted the functions and targeted genes of these differentially expressed miRNAs, i.e. Akt3, FGFR3, PSEN1, VEGFa and AR. Subsequently, expression of the selected differentially expressed miRNAs (Hsa-miR-4795-5p, Hsa-miR-488, Hsa-miR-4784, Hsa-miR-330, Hsa-miR-3916, Hsa-miR-4274 and Hsa-miR-181c) was validated in another set of tissue samples. A total of 29 miRNAs were identified to be differentially expressed between AAN-UUC and non-AAN-UUC tissues and these miRNA target genes in FGFR3 and Akt pathways, which regulate cell growth and tumor progression, respectively. D.A. Spandidos 2015-11 2015-09-15 /pmc/articles/PMC4626193/ /pubmed/26397152 http://dx.doi.org/10.3892/mmr.2015.4330 Text en Copyright: © Tao et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
TAO, LE
ZENG, YIGANG
WANG, JUN
LIU, ZHIHONG
SHEN, BING
GE, JIFU
LIU, YONG
GUO, YIFENG
QIU, JIANXIN
Differential microRNA expression in aristolochic acid-induced upper urothelial tract cancers ex vivo
title Differential microRNA expression in aristolochic acid-induced upper urothelial tract cancers ex vivo
title_full Differential microRNA expression in aristolochic acid-induced upper urothelial tract cancers ex vivo
title_fullStr Differential microRNA expression in aristolochic acid-induced upper urothelial tract cancers ex vivo
title_full_unstemmed Differential microRNA expression in aristolochic acid-induced upper urothelial tract cancers ex vivo
title_short Differential microRNA expression in aristolochic acid-induced upper urothelial tract cancers ex vivo
title_sort differential microrna expression in aristolochic acid-induced upper urothelial tract cancers ex vivo
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626193/
https://www.ncbi.nlm.nih.gov/pubmed/26397152
http://dx.doi.org/10.3892/mmr.2015.4330
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