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Microarray profile of human kidney from diabetes, renal cell carcinoma and renal cell carcinoma with diabetes

Recent study from our laboratory showed that patients with diabetes are at a higher risk of developing kidney cancer. In the current study, we have screened whole human DNA genome from healthy control, patients with diabetes or renal cell carcinoma (RCC) or RCC+diabetes. We found that 883 genes gain...

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Autores principales: Kosti, Adam, Harry Chen, Hung-I, Mohan, Sumathy, Liang, Sitai, Chen, Yidong, Habib, Samy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362485/
https://www.ncbi.nlm.nih.gov/pubmed/25821562
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author Kosti, Adam
Harry Chen, Hung-I
Mohan, Sumathy
Liang, Sitai
Chen, Yidong
Habib, Samy L.
author_facet Kosti, Adam
Harry Chen, Hung-I
Mohan, Sumathy
Liang, Sitai
Chen, Yidong
Habib, Samy L.
author_sort Kosti, Adam
collection PubMed
description Recent study from our laboratory showed that patients with diabetes are at a higher risk of developing kidney cancer. In the current study, we have screened whole human DNA genome from healthy control, patients with diabetes or renal cell carcinoma (RCC) or RCC+diabetes. We found that 883 genes gain/163 genes loss of copy number in RCC+diabetes group, 669 genes gain/307 genes loss in RCC group and 458 genes gain/38 genes loss of copy number in diabetes group, after removing gain/loss genes obtained from healthy control group. Data analyzed for functional annotation enrichment pathways showed that control group had the highest number (280) of enriched pathways, 191 in diabetes+RCC group, 148 in RCC group, and 81 in diabetes group. The overlap GO pathways between RCC+diabetes and RCC groups showed that nine were enriched, between RCC+diabetes and diabetes groups was four and between diabetes and RCC groups was eight GO pathways. Overall, we observed majority of DNA alterations in patients from RCC+diabetes group. Interestingly, insulin receptor (INSR) is highly expressed and had gains in copy number in RCC+diabetes and diabetes groups. The changes in INSR copy number may use as a biomarker for predicting RCC development in diabetic patients.
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spelling pubmed-43624852015-03-27 Microarray profile of human kidney from diabetes, renal cell carcinoma and renal cell carcinoma with diabetes Kosti, Adam Harry Chen, Hung-I Mohan, Sumathy Liang, Sitai Chen, Yidong Habib, Samy L. Genes Cancer Research Paper Recent study from our laboratory showed that patients with diabetes are at a higher risk of developing kidney cancer. In the current study, we have screened whole human DNA genome from healthy control, patients with diabetes or renal cell carcinoma (RCC) or RCC+diabetes. We found that 883 genes gain/163 genes loss of copy number in RCC+diabetes group, 669 genes gain/307 genes loss in RCC group and 458 genes gain/38 genes loss of copy number in diabetes group, after removing gain/loss genes obtained from healthy control group. Data analyzed for functional annotation enrichment pathways showed that control group had the highest number (280) of enriched pathways, 191 in diabetes+RCC group, 148 in RCC group, and 81 in diabetes group. The overlap GO pathways between RCC+diabetes and RCC groups showed that nine were enriched, between RCC+diabetes and diabetes groups was four and between diabetes and RCC groups was eight GO pathways. Overall, we observed majority of DNA alterations in patients from RCC+diabetes group. Interestingly, insulin receptor (INSR) is highly expressed and had gains in copy number in RCC+diabetes and diabetes groups. The changes in INSR copy number may use as a biomarker for predicting RCC development in diabetic patients. Impact Journals LLC 2015-01 /pmc/articles/PMC4362485/ /pubmed/25821562 Text en Copyright: © 2015 Kosti et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Kosti, Adam
Harry Chen, Hung-I
Mohan, Sumathy
Liang, Sitai
Chen, Yidong
Habib, Samy L.
Microarray profile of human kidney from diabetes, renal cell carcinoma and renal cell carcinoma with diabetes
title Microarray profile of human kidney from diabetes, renal cell carcinoma and renal cell carcinoma with diabetes
title_full Microarray profile of human kidney from diabetes, renal cell carcinoma and renal cell carcinoma with diabetes
title_fullStr Microarray profile of human kidney from diabetes, renal cell carcinoma and renal cell carcinoma with diabetes
title_full_unstemmed Microarray profile of human kidney from diabetes, renal cell carcinoma and renal cell carcinoma with diabetes
title_short Microarray profile of human kidney from diabetes, renal cell carcinoma and renal cell carcinoma with diabetes
title_sort microarray profile of human kidney from diabetes, renal cell carcinoma and renal cell carcinoma with diabetes
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362485/
https://www.ncbi.nlm.nih.gov/pubmed/25821562
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