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Meta-analysis of gene expression profiling reveals novel basal gene signatures in MCF-10A cells transformed with cadmium

Cadmium (Cd(2+)) is an environmental toxicant and a human carcinogen. Several studies show an association of Cd(2+) exposure to the development of breast cancer. Previously, we have transformed the immortalized non-tumorigenic cell line MCF-10A with Cd(2+) and have demonstrated that the transformed...

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Autores principales: Blommel, Katrina, Knudsen, Carley S., Wegner, Kyle, Shrestha, Swojani, Singhal, Sandeep K., Mehus, Aaron A., Garrett, Scott H., Singhal, Sonalika, Zhou, Xudong, Voels, Brent, Sens, Donald A., Somji, Seema
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533076/
https://www.ncbi.nlm.nih.gov/pubmed/33062196
http://dx.doi.org/10.18632/oncotarget.27734
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author Blommel, Katrina
Knudsen, Carley S.
Wegner, Kyle
Shrestha, Swojani
Singhal, Sandeep K.
Mehus, Aaron A.
Garrett, Scott H.
Singhal, Sonalika
Zhou, Xudong
Voels, Brent
Sens, Donald A.
Somji, Seema
author_facet Blommel, Katrina
Knudsen, Carley S.
Wegner, Kyle
Shrestha, Swojani
Singhal, Sandeep K.
Mehus, Aaron A.
Garrett, Scott H.
Singhal, Sonalika
Zhou, Xudong
Voels, Brent
Sens, Donald A.
Somji, Seema
author_sort Blommel, Katrina
collection PubMed
description Cadmium (Cd(2+)) is an environmental toxicant and a human carcinogen. Several studies show an association of Cd(2+) exposure to the development of breast cancer. Previously, we have transformed the immortalized non-tumorigenic cell line MCF-10A with Cd(2+) and have demonstrated that the transformed cells have anchorage independent growth. In a separate study, we showed that transformation of the immortalized urothelial cells with the environmental carcinogen arsenite (As(3+)) results in an increase in expression of genes associated with the basal subtype of bladder cancer. In this study, we determined if transformation of the MCF-10A cells with Cd(2+) would have a similar effect on the expression of basal genes. The results of our study indicate that there is a decrease in expression of genes associated with keratinization and cornification and this gene signature includes the genes associated with the basal subtype of breast cancer. An analysis of human breast cancer databases indicates an increased expression of this gene signature is associated with a positive correlation to patient survival whereas a reduced expression/absence of this gene signature is associated with poor patient survival. Thus, our study suggests that transformation of the MCF-10A cells with Cd(2+) produces a decreased basal gene expression profile that correlates to patient outcome.
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spelling pubmed-75330762020-10-13 Meta-analysis of gene expression profiling reveals novel basal gene signatures in MCF-10A cells transformed with cadmium Blommel, Katrina Knudsen, Carley S. Wegner, Kyle Shrestha, Swojani Singhal, Sandeep K. Mehus, Aaron A. Garrett, Scott H. Singhal, Sonalika Zhou, Xudong Voels, Brent Sens, Donald A. Somji, Seema Oncotarget Meta-Analysis Cadmium (Cd(2+)) is an environmental toxicant and a human carcinogen. Several studies show an association of Cd(2+) exposure to the development of breast cancer. Previously, we have transformed the immortalized non-tumorigenic cell line MCF-10A with Cd(2+) and have demonstrated that the transformed cells have anchorage independent growth. In a separate study, we showed that transformation of the immortalized urothelial cells with the environmental carcinogen arsenite (As(3+)) results in an increase in expression of genes associated with the basal subtype of bladder cancer. In this study, we determined if transformation of the MCF-10A cells with Cd(2+) would have a similar effect on the expression of basal genes. The results of our study indicate that there is a decrease in expression of genes associated with keratinization and cornification and this gene signature includes the genes associated with the basal subtype of breast cancer. An analysis of human breast cancer databases indicates an increased expression of this gene signature is associated with a positive correlation to patient survival whereas a reduced expression/absence of this gene signature is associated with poor patient survival. Thus, our study suggests that transformation of the MCF-10A cells with Cd(2+) produces a decreased basal gene expression profile that correlates to patient outcome. Impact Journals LLC 2020-09-29 /pmc/articles/PMC7533076/ /pubmed/33062196 http://dx.doi.org/10.18632/oncotarget.27734 Text en https://creativecommons.org/licenses/by/3.0/ Copyright: © 2020 Blommel et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are cited.
spellingShingle Meta-Analysis
Blommel, Katrina
Knudsen, Carley S.
Wegner, Kyle
Shrestha, Swojani
Singhal, Sandeep K.
Mehus, Aaron A.
Garrett, Scott H.
Singhal, Sonalika
Zhou, Xudong
Voels, Brent
Sens, Donald A.
Somji, Seema
Meta-analysis of gene expression profiling reveals novel basal gene signatures in MCF-10A cells transformed with cadmium
title Meta-analysis of gene expression profiling reveals novel basal gene signatures in MCF-10A cells transformed with cadmium
title_full Meta-analysis of gene expression profiling reveals novel basal gene signatures in MCF-10A cells transformed with cadmium
title_fullStr Meta-analysis of gene expression profiling reveals novel basal gene signatures in MCF-10A cells transformed with cadmium
title_full_unstemmed Meta-analysis of gene expression profiling reveals novel basal gene signatures in MCF-10A cells transformed with cadmium
title_short Meta-analysis of gene expression profiling reveals novel basal gene signatures in MCF-10A cells transformed with cadmium
title_sort meta-analysis of gene expression profiling reveals novel basal gene signatures in mcf-10a cells transformed with cadmium
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533076/
https://www.ncbi.nlm.nih.gov/pubmed/33062196
http://dx.doi.org/10.18632/oncotarget.27734
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