The interaction between MALAT1 target, miR-143-3p, and RALGAPA2 is affected by functional SNP rs3827693 in breast cancer.


Journal

Human cell
ISSN: 1749-0774
Titre abrégé: Hum Cell
Pays: Japan
ID NLM: 8912329

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 04 06 2020
accepted: 26 08 2020
pubmed: 4 9 2020
medline: 28 10 2020
entrez: 4 9 2020
Statut: ppublish

Résumé

A higher expression of MALAT1 has been reported in breast cancer. However, more studies are needed to decipher the mechanisms by which this lncRNA imposes its oncogenic effects. In this study, blood and tissue samples were taken from healthy normal and breast cancer subjects. qPCR was used to analyze the gene expression. HRM-PCR method was carried out to genotype the selected samples. Computational analysis was recruited to find novel targets of MALAT1 and miR-143-3p. The data analyses revealed that MALAT1 was up-regulated in breast cancer and could be a distinctive factor to diagnose cancer. The expression of MALAT1 was inversely correlated with miR-143-3p expression in the studied clinical samples. The down-regulation of miR-143-3p was proven in the clinical tumor samples as compared to the healthy controls. A negative correlation of miR-143-3p with its putative target, RALGAPA2 was observed. A functional SNP rs3827693 located within the 3'UTR region of RALGAPA2 mRNA was validated in this study to associate with breast cancer risk. The rs3827693 allele G significantly decreased the breast cancer incidence and augmented the negative correlation between RALGAPA2 and miR-143-3p, presumably through strengthening the interaction between these two transcripts. This study proposed MALAT1 miR-143-3p and miR-143-3p RALGAPA2 axis in breast cancer, whereby the latter can be altered by the clinically functional SNP rs3827693.

Identifiants

pubmed: 32880825
doi: 10.1007/s13577-020-00422-x
pii: 10.1007/s13577-020-00422-x
doi:

Substances chimiques

GTPase-Activating Proteins 0
MALAT1 long non-coding RNA, human 0
MIRN143 microRNA, human 0
MicroRNAs 0
RALGAPA2 protein, human 0
RNA, Long Noncoding 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1229-1239

Références

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Auteurs

Nasrin Fattahi Dolatabadi (N)

Zist-Fanavari Novin Biotechnology Institute, Isfahan, Iran.

Arezo Dehghani (A)

Zist-Fanavari Novin Biotechnology Institute, Isfahan, Iran.

Elham Shahand (E)

Zist-Fanavari Novin Biotechnology Institute, Isfahan, Iran.

Mohammadreza Yazdanshenas (M)

Zist-Fanavari Novin Biotechnology Institute, Isfahan, Iran.

Hossein Tabatabaeian (H)

Department of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran. csiht@nus.edu.sg.
Anahid Breast Cancer Clinic, Isfahan Healthcare City, Isfahan, Iran. csiht@nus.edu.sg.

Atefe Zamani (A)

Zist-Fanavari Novin Biotechnology Institute, Isfahan, Iran.

Mansoureh Azadeh (M)

Zist-Fanavari Novin Biotechnology Institute, Isfahan, Iran.

Kamran Ghaedi (K)

Department of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran. kamranghaedi@sci.ui.ac.ir.
Department of Cellular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran. kamranghaedi@sci.ui.ac.ir.

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