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LAMA4-Regulating miR-4274 and Its Host Gene SORCS2 Play a Role in IGFBP6-Dependent Effects on Phenotype of Basal-Like Breast Cancer

Specificity of RNAi to selected target is challenged by off-target effects, both canonical and non-canonical. Notably, more than half of all human microRNAs are co-expressed with hosting them proteincoding genes. Here we dissect regulatory subnetwork centered on IGFBP6 gene, which is associated with...

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Autores principales: Shkurnikov, Maxim, Nikulin, Sergey, Nersisyan, Stepan, Poloznikov, Andrey, Zaidi, Shan, Baranova, Ancha, Schumacher, Udo, Wicklein, Daniel, Tonevitsky, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857517/
https://www.ncbi.nlm.nih.gov/pubmed/31781574
http://dx.doi.org/10.3389/fmolb.2019.00122
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author Shkurnikov, Maxim
Nikulin, Sergey
Nersisyan, Stepan
Poloznikov, Andrey
Zaidi, Shan
Baranova, Ancha
Schumacher, Udo
Wicklein, Daniel
Tonevitsky, Alexander
author_facet Shkurnikov, Maxim
Nikulin, Sergey
Nersisyan, Stepan
Poloznikov, Andrey
Zaidi, Shan
Baranova, Ancha
Schumacher, Udo
Wicklein, Daniel
Tonevitsky, Alexander
author_sort Shkurnikov, Maxim
collection PubMed
description Specificity of RNAi to selected target is challenged by off-target effects, both canonical and non-canonical. Notably, more than half of all human microRNAs are co-expressed with hosting them proteincoding genes. Here we dissect regulatory subnetwork centered on IGFBP6 gene, which is associated with low proliferative state and high migratory activity of basal-like breast cancer. We inhibited expression of IGFBP6 gene in a model cell line for basal-like breast carcinoma MDA-MB-231, then traced secondary and tertiary effects of this knockdown to LAMA4, a laminin encoding gene that contributes to the phenotype of triple-negative breast cancer. LAMA4-regulating miRNA miR-4274 and its host gene SORCS2 were highlighted as intermediate regulators of the expression levels of LAMA4, which correlated in a basal-like breast carcinoma sample subset of TCGA to the levels of SORCS2 negatively. Overall, our study points that the secondary and tertiary layers of regulatory interactions are certainly underappreciated. As these types of molecular event may significantly contribute to the formation of the cell phenotypes after RNA interference based knockdowns, further studies of multilayered molecular networks affected by RNAi are warranted.
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spelling pubmed-68575172019-11-28 LAMA4-Regulating miR-4274 and Its Host Gene SORCS2 Play a Role in IGFBP6-Dependent Effects on Phenotype of Basal-Like Breast Cancer Shkurnikov, Maxim Nikulin, Sergey Nersisyan, Stepan Poloznikov, Andrey Zaidi, Shan Baranova, Ancha Schumacher, Udo Wicklein, Daniel Tonevitsky, Alexander Front Mol Biosci Molecular Biosciences Specificity of RNAi to selected target is challenged by off-target effects, both canonical and non-canonical. Notably, more than half of all human microRNAs are co-expressed with hosting them proteincoding genes. Here we dissect regulatory subnetwork centered on IGFBP6 gene, which is associated with low proliferative state and high migratory activity of basal-like breast cancer. We inhibited expression of IGFBP6 gene in a model cell line for basal-like breast carcinoma MDA-MB-231, then traced secondary and tertiary effects of this knockdown to LAMA4, a laminin encoding gene that contributes to the phenotype of triple-negative breast cancer. LAMA4-regulating miRNA miR-4274 and its host gene SORCS2 were highlighted as intermediate regulators of the expression levels of LAMA4, which correlated in a basal-like breast carcinoma sample subset of TCGA to the levels of SORCS2 negatively. Overall, our study points that the secondary and tertiary layers of regulatory interactions are certainly underappreciated. As these types of molecular event may significantly contribute to the formation of the cell phenotypes after RNA interference based knockdowns, further studies of multilayered molecular networks affected by RNAi are warranted. Frontiers Media S.A. 2019-11-08 /pmc/articles/PMC6857517/ /pubmed/31781574 http://dx.doi.org/10.3389/fmolb.2019.00122 Text en Copyright © 2019 Shkurnikov, Nikulin, Nersisyan, Poloznikov, Zaidi, Baranova, Schumacher, Wicklein and Tonevitsky. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Biosciences
Shkurnikov, Maxim
Nikulin, Sergey
Nersisyan, Stepan
Poloznikov, Andrey
Zaidi, Shan
Baranova, Ancha
Schumacher, Udo
Wicklein, Daniel
Tonevitsky, Alexander
LAMA4-Regulating miR-4274 and Its Host Gene SORCS2 Play a Role in IGFBP6-Dependent Effects on Phenotype of Basal-Like Breast Cancer
title LAMA4-Regulating miR-4274 and Its Host Gene SORCS2 Play a Role in IGFBP6-Dependent Effects on Phenotype of Basal-Like Breast Cancer
title_full LAMA4-Regulating miR-4274 and Its Host Gene SORCS2 Play a Role in IGFBP6-Dependent Effects on Phenotype of Basal-Like Breast Cancer
title_fullStr LAMA4-Regulating miR-4274 and Its Host Gene SORCS2 Play a Role in IGFBP6-Dependent Effects on Phenotype of Basal-Like Breast Cancer
title_full_unstemmed LAMA4-Regulating miR-4274 and Its Host Gene SORCS2 Play a Role in IGFBP6-Dependent Effects on Phenotype of Basal-Like Breast Cancer
title_short LAMA4-Regulating miR-4274 and Its Host Gene SORCS2 Play a Role in IGFBP6-Dependent Effects on Phenotype of Basal-Like Breast Cancer
title_sort lama4-regulating mir-4274 and its host gene sorcs2 play a role in igfbp6-dependent effects on phenotype of basal-like breast cancer
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857517/
https://www.ncbi.nlm.nih.gov/pubmed/31781574
http://dx.doi.org/10.3389/fmolb.2019.00122
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