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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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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. |
format | Online Article Text |
id | pubmed-4362485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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