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Gender-Associated Genomic Differences in Colorectal Cancer: Clinical Insight from Feminization of Male Cancer Cells

Gender-related differences in colorectal cancer (CRC) are not fully understood. Recent studies have shown that CRC arising in females are significantly associated with CpG island methylator phenotype (CIMP-high). Using array comparative genomic hybridization, we analyzed a cohort of 116 CRCs (57 mal...

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Autores principales: Ali, Rola H., Marafie, Makia J., Bitar, Milad S., Al-Dousari, Fahad, Ismael, Samar, Bin Haider, Hussain, Al-Ali, Waleed, Jacob, Sindhu P., Al-Mulla, Fahd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227166/
https://www.ncbi.nlm.nih.gov/pubmed/25268611
http://dx.doi.org/10.3390/ijms151017344
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author Ali, Rola H.
Marafie, Makia J.
Bitar, Milad S.
Al-Dousari, Fahad
Ismael, Samar
Bin Haider, Hussain
Al-Ali, Waleed
Jacob, Sindhu P.
Al-Mulla, Fahd
author_facet Ali, Rola H.
Marafie, Makia J.
Bitar, Milad S.
Al-Dousari, Fahad
Ismael, Samar
Bin Haider, Hussain
Al-Ali, Waleed
Jacob, Sindhu P.
Al-Mulla, Fahd
author_sort Ali, Rola H.
collection PubMed
description Gender-related differences in colorectal cancer (CRC) are not fully understood. Recent studies have shown that CRC arising in females are significantly associated with CpG island methylator phenotype (CIMP-high). Using array comparative genomic hybridization, we analyzed a cohort of 116 CRCs (57 males, 59 females) for chromosomal copy number aberrations (CNA) and found that CRC in females had significantly higher numbers of gains involving chromosome arms 1q21.2–q21.3, 4q13.2, 6p21.1 and 16p11.2 and copy number losses of chromosome arm 11q25 compared to males. Interestingly, a subset of male CRCs (46%) exhibited a “feminization” phenomenon in the form of gains of X chromosomes (or an arm of X) and/or losses of the Y chromosome. Feminization of cancer cells was significantly associated with microsatellite-stable CRCs (p-value 0.003) and wild-type BRAF gene status (p-value 0.009). No significant association with other clinicopathological parameters was identified including disease-free survival. In summary, our data show that some CNAs in CRC may be gender specific and that male cancers characterized by feminization may constitute a specific subset of CRCs that warrants further investigation.
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spelling pubmed-42271662014-11-12 Gender-Associated Genomic Differences in Colorectal Cancer: Clinical Insight from Feminization of Male Cancer Cells Ali, Rola H. Marafie, Makia J. Bitar, Milad S. Al-Dousari, Fahad Ismael, Samar Bin Haider, Hussain Al-Ali, Waleed Jacob, Sindhu P. Al-Mulla, Fahd Int J Mol Sci Article Gender-related differences in colorectal cancer (CRC) are not fully understood. Recent studies have shown that CRC arising in females are significantly associated with CpG island methylator phenotype (CIMP-high). Using array comparative genomic hybridization, we analyzed a cohort of 116 CRCs (57 males, 59 females) for chromosomal copy number aberrations (CNA) and found that CRC in females had significantly higher numbers of gains involving chromosome arms 1q21.2–q21.3, 4q13.2, 6p21.1 and 16p11.2 and copy number losses of chromosome arm 11q25 compared to males. Interestingly, a subset of male CRCs (46%) exhibited a “feminization” phenomenon in the form of gains of X chromosomes (or an arm of X) and/or losses of the Y chromosome. Feminization of cancer cells was significantly associated with microsatellite-stable CRCs (p-value 0.003) and wild-type BRAF gene status (p-value 0.009). No significant association with other clinicopathological parameters was identified including disease-free survival. In summary, our data show that some CNAs in CRC may be gender specific and that male cancers characterized by feminization may constitute a specific subset of CRCs that warrants further investigation. MDPI 2014-09-29 /pmc/articles/PMC4227166/ /pubmed/25268611 http://dx.doi.org/10.3390/ijms151017344 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ali, Rola H.
Marafie, Makia J.
Bitar, Milad S.
Al-Dousari, Fahad
Ismael, Samar
Bin Haider, Hussain
Al-Ali, Waleed
Jacob, Sindhu P.
Al-Mulla, Fahd
Gender-Associated Genomic Differences in Colorectal Cancer: Clinical Insight from Feminization of Male Cancer Cells
title Gender-Associated Genomic Differences in Colorectal Cancer: Clinical Insight from Feminization of Male Cancer Cells
title_full Gender-Associated Genomic Differences in Colorectal Cancer: Clinical Insight from Feminization of Male Cancer Cells
title_fullStr Gender-Associated Genomic Differences in Colorectal Cancer: Clinical Insight from Feminization of Male Cancer Cells
title_full_unstemmed Gender-Associated Genomic Differences in Colorectal Cancer: Clinical Insight from Feminization of Male Cancer Cells
title_short Gender-Associated Genomic Differences in Colorectal Cancer: Clinical Insight from Feminization of Male Cancer Cells
title_sort gender-associated genomic differences in colorectal cancer: clinical insight from feminization of male cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227166/
https://www.ncbi.nlm.nih.gov/pubmed/25268611
http://dx.doi.org/10.3390/ijms151017344
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