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Phenotypic and microRNA transcriptomic profiling of the MDA-MB-231 spheroid-enriched CSCs with comparison of MCF-7 microRNA profiling dataset

Breast cancer spheroids have been widely used as in vitro models of cancer stem cells (CSCs), yet little is known about their phenotypic characteristics and microRNAs (miRNAs) expression profiles. The objectives of this research were to evaluate the phenotypic characteristics of MDA-MB-231 spheroid-...

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Detalles Bibliográficos
Autores principales: Boo, Lily, Ho, Wan Yong, Mohd Ali, Norlaily, Yeap, Swee Keong, Ky, Huynh, Chan, Kok Gan, Yin, Wai Fong, Satharasinghe, Dilan Amila, Liew, Woan Charn, Tan, Sheau Wei, Cheong, Soon Keng, Ong, Han Kiat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511503/
https://www.ncbi.nlm.nih.gov/pubmed/28717596
http://dx.doi.org/10.7717/peerj.3551
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author Boo, Lily
Ho, Wan Yong
Mohd Ali, Norlaily
Yeap, Swee Keong
Ky, Huynh
Chan, Kok Gan
Yin, Wai Fong
Satharasinghe, Dilan Amila
Liew, Woan Charn
Tan, Sheau Wei
Cheong, Soon Keng
Ong, Han Kiat
author_facet Boo, Lily
Ho, Wan Yong
Mohd Ali, Norlaily
Yeap, Swee Keong
Ky, Huynh
Chan, Kok Gan
Yin, Wai Fong
Satharasinghe, Dilan Amila
Liew, Woan Charn
Tan, Sheau Wei
Cheong, Soon Keng
Ong, Han Kiat
author_sort Boo, Lily
collection PubMed
description Breast cancer spheroids have been widely used as in vitro models of cancer stem cells (CSCs), yet little is known about their phenotypic characteristics and microRNAs (miRNAs) expression profiles. The objectives of this research were to evaluate the phenotypic characteristics of MDA-MB-231 spheroid-enriched cells for their CSCs properties and also to determine their miRNAs expression profile. Similar to our previously published MCF-7 spheroid, MDA-MB-231 spheroid also showed typical CSCs characteristics namely self-renewability, expression of putative CSCs-related surface markers and enhancement of drug resistance. From the miRNA profile, miR-15b, miR-34a, miR-148a, miR-628 and miR-196b were shown to be involved in CSCs-associated signalling pathways in both models of spheroids, which highlights the involvement of these miRNAs in maintaining the CSCs features. In addition, unique clusters of miRNAs namely miR-205, miR-181a and miR-204 were found in basal-like spheroid whereas miR-125, miR-760, miR-30c and miR-136 were identified in luminal-like spheroid. Our results highlight the roles of miRNAs as well as novel perspectives of the relevant pathways underlying spheroid-enriched CSCs in breast cancer.
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spelling pubmed-55115032017-07-17 Phenotypic and microRNA transcriptomic profiling of the MDA-MB-231 spheroid-enriched CSCs with comparison of MCF-7 microRNA profiling dataset Boo, Lily Ho, Wan Yong Mohd Ali, Norlaily Yeap, Swee Keong Ky, Huynh Chan, Kok Gan Yin, Wai Fong Satharasinghe, Dilan Amila Liew, Woan Charn Tan, Sheau Wei Cheong, Soon Keng Ong, Han Kiat PeerJ Cell Biology Breast cancer spheroids have been widely used as in vitro models of cancer stem cells (CSCs), yet little is known about their phenotypic characteristics and microRNAs (miRNAs) expression profiles. The objectives of this research were to evaluate the phenotypic characteristics of MDA-MB-231 spheroid-enriched cells for their CSCs properties and also to determine their miRNAs expression profile. Similar to our previously published MCF-7 spheroid, MDA-MB-231 spheroid also showed typical CSCs characteristics namely self-renewability, expression of putative CSCs-related surface markers and enhancement of drug resistance. From the miRNA profile, miR-15b, miR-34a, miR-148a, miR-628 and miR-196b were shown to be involved in CSCs-associated signalling pathways in both models of spheroids, which highlights the involvement of these miRNAs in maintaining the CSCs features. In addition, unique clusters of miRNAs namely miR-205, miR-181a and miR-204 were found in basal-like spheroid whereas miR-125, miR-760, miR-30c and miR-136 were identified in luminal-like spheroid. Our results highlight the roles of miRNAs as well as novel perspectives of the relevant pathways underlying spheroid-enriched CSCs in breast cancer. PeerJ Inc. 2017-07-13 /pmc/articles/PMC5511503/ /pubmed/28717596 http://dx.doi.org/10.7717/peerj.3551 Text en ©2017 Boo et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Cell Biology
Boo, Lily
Ho, Wan Yong
Mohd Ali, Norlaily
Yeap, Swee Keong
Ky, Huynh
Chan, Kok Gan
Yin, Wai Fong
Satharasinghe, Dilan Amila
Liew, Woan Charn
Tan, Sheau Wei
Cheong, Soon Keng
Ong, Han Kiat
Phenotypic and microRNA transcriptomic profiling of the MDA-MB-231 spheroid-enriched CSCs with comparison of MCF-7 microRNA profiling dataset
title Phenotypic and microRNA transcriptomic profiling of the MDA-MB-231 spheroid-enriched CSCs with comparison of MCF-7 microRNA profiling dataset
title_full Phenotypic and microRNA transcriptomic profiling of the MDA-MB-231 spheroid-enriched CSCs with comparison of MCF-7 microRNA profiling dataset
title_fullStr Phenotypic and microRNA transcriptomic profiling of the MDA-MB-231 spheroid-enriched CSCs with comparison of MCF-7 microRNA profiling dataset
title_full_unstemmed Phenotypic and microRNA transcriptomic profiling of the MDA-MB-231 spheroid-enriched CSCs with comparison of MCF-7 microRNA profiling dataset
title_short Phenotypic and microRNA transcriptomic profiling of the MDA-MB-231 spheroid-enriched CSCs with comparison of MCF-7 microRNA profiling dataset
title_sort phenotypic and microrna transcriptomic profiling of the mda-mb-231 spheroid-enriched cscs with comparison of mcf-7 microrna profiling dataset
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511503/
https://www.ncbi.nlm.nih.gov/pubmed/28717596
http://dx.doi.org/10.7717/peerj.3551
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