Epigenetic Alterations of Chromosome 3 Revealed by NotI-Microarrays in Clear Cell Renal Cell Carcinoma
This study aimed to clarify epigenetic and genetic alterations that occur during renal carcinogenesis. The original method includes chromosome 3 specific NotI-microarrays containing 180 NotI-clones associated with 188 genes for hybridization with 23 paired normal/tumor DNA samples of primary clear c...
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doaj-afeaa1619b174f018672db955441002a2020-11-24T23:58:10ZengHindawi LimitedBioMed Research International2314-61332314-61412014-01-01201410.1155/2014/735292735292Epigenetic Alterations of Chromosome 3 Revealed by NotI-Microarrays in Clear Cell Renal Cell CarcinomaAlexey A. Dmitriev0Evgeniya E. Rudenko1Anna V. Kudryavtseva2George S. Krasnov3Vasily V. Gordiyuk4Nataliya V. Melnikova5Eduard O. Stakhovsky6Oleksii A. Kononenko7Larissa S. Pavlova8Tatiana T. Kondratieva9Boris Y. Alekseev10Eleonora A. Braga11Vera N. Senchenko12Vladimir I. Kashuba13Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, RussiaInstitute of Molecular Biology and Genetics, Ukrainian Academy of Sciences, Kiev 03680, UkraineEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, RussiaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, RussiaInstitute of Molecular Biology and Genetics, Ukrainian Academy of Sciences, Kiev 03680, UkraineEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, RussiaNational Cancer Institute, Kiev 03022, UkraineNational Cancer Institute, Kiev 03022, UkraineN.N. Blokhin Russian Cancer Research Center, Russian Academy of Medical Sciences, Moscow 115478, RussiaN.N. Blokhin Russian Cancer Research Center, Russian Academy of Medical Sciences, Moscow 115478, RussiaP.A. Herzen Moscow Oncology Research Institute, Ministry of Healthcare of the Russian Federation, Moscow 125284, RussiaInstitute of General Pathology and Pathophysiology, Russian Academy of Medical Sciences, Moscow 125315, RussiaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, RussiaInstitute of Molecular Biology and Genetics, Ukrainian Academy of Sciences, Kiev 03680, UkraineThis study aimed to clarify epigenetic and genetic alterations that occur during renal carcinogenesis. The original method includes chromosome 3 specific NotI-microarrays containing 180 NotI-clones associated with 188 genes for hybridization with 23 paired normal/tumor DNA samples of primary clear cell renal cell carcinomas (ccRCC). Twenty-two genes showed methylation and/or deletion in 17–57% of tumors. These genes include tumor suppressors or candidates (VHL, CTDSPL, LRRC3B, ALDH1L1, and EPHB1) and genes that were not previously considered as cancer-associated (e.g., LRRN1, GORASP1, FGD5, and PLCL2). Bisulfite sequencing analysis confirmed methylation as a frequent event in ccRCC. A set of six markers (NKIRAS1/RPL15, LRRN1, LRRC3B, CTDSPL, GORASP1/TTC21A, and VHL) was suggested for ccRCC detection in renal biopsies. The mRNA level decrease was shown for 6 NotI-associated genes in ccRCC using quantitative PCR: LRRN1, GORASP1, FOXP1, FGD5, PLCL2, and ALDH1L1. The majority of examined genes showed distinct expression profiles in ccRCC and papillary RCC. The strongest extent and frequency of downregulation were shown for ALDH1L1 gene both in ccRCC and papillary RCC. Moreover, the extent of ALDH1L1 mRNA level decrease was more pronounced in both histological types of RCC stage III compared with stages I and II (P=0.03). The same was observed for FGD5 gene in ccRCC (P<0.06).http://dx.doi.org/10.1155/2014/735292 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alexey A. Dmitriev Evgeniya E. Rudenko Anna V. Kudryavtseva George S. Krasnov Vasily V. Gordiyuk Nataliya V. Melnikova Eduard O. Stakhovsky Oleksii A. Kononenko Larissa S. Pavlova Tatiana T. Kondratieva Boris Y. Alekseev Eleonora A. Braga Vera N. Senchenko Vladimir I. Kashuba |
spellingShingle |
Alexey A. Dmitriev Evgeniya E. Rudenko Anna V. Kudryavtseva George S. Krasnov Vasily V. Gordiyuk Nataliya V. Melnikova Eduard O. Stakhovsky Oleksii A. Kononenko Larissa S. Pavlova Tatiana T. Kondratieva Boris Y. Alekseev Eleonora A. Braga Vera N. Senchenko Vladimir I. Kashuba Epigenetic Alterations of Chromosome 3 Revealed by NotI-Microarrays in Clear Cell Renal Cell Carcinoma BioMed Research International |
author_facet |
Alexey A. Dmitriev Evgeniya E. Rudenko Anna V. Kudryavtseva George S. Krasnov Vasily V. Gordiyuk Nataliya V. Melnikova Eduard O. Stakhovsky Oleksii A. Kononenko Larissa S. Pavlova Tatiana T. Kondratieva Boris Y. Alekseev Eleonora A. Braga Vera N. Senchenko Vladimir I. Kashuba |
author_sort |
Alexey A. Dmitriev |
title |
Epigenetic Alterations of Chromosome 3 Revealed by NotI-Microarrays in Clear Cell Renal Cell Carcinoma |
title_short |
Epigenetic Alterations of Chromosome 3 Revealed by NotI-Microarrays in Clear Cell Renal Cell Carcinoma |
title_full |
Epigenetic Alterations of Chromosome 3 Revealed by NotI-Microarrays in Clear Cell Renal Cell Carcinoma |
title_fullStr |
Epigenetic Alterations of Chromosome 3 Revealed by NotI-Microarrays in Clear Cell Renal Cell Carcinoma |
title_full_unstemmed |
Epigenetic Alterations of Chromosome 3 Revealed by NotI-Microarrays in Clear Cell Renal Cell Carcinoma |
title_sort |
epigenetic alterations of chromosome 3 revealed by noti-microarrays in clear cell renal cell carcinoma |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2014-01-01 |
description |
This study aimed to clarify epigenetic and genetic alterations that occur during renal carcinogenesis. The original method includes chromosome 3 specific NotI-microarrays containing 180 NotI-clones associated with 188 genes for hybridization with 23 paired normal/tumor DNA samples of primary clear cell renal cell carcinomas (ccRCC). Twenty-two genes showed methylation and/or deletion in 17–57% of tumors. These genes include tumor suppressors or candidates (VHL, CTDSPL, LRRC3B, ALDH1L1, and EPHB1) and genes that were not previously considered as cancer-associated (e.g., LRRN1, GORASP1, FGD5, and PLCL2). Bisulfite sequencing analysis confirmed methylation as a frequent event in ccRCC. A set of six markers (NKIRAS1/RPL15, LRRN1, LRRC3B, CTDSPL, GORASP1/TTC21A, and VHL) was suggested for ccRCC detection in renal biopsies. The mRNA level decrease was shown for 6 NotI-associated genes in ccRCC using quantitative PCR: LRRN1, GORASP1, FOXP1, FGD5, PLCL2, and ALDH1L1. The majority of examined genes showed distinct expression profiles in ccRCC and papillary RCC. The strongest extent and frequency of downregulation were shown for ALDH1L1 gene both in ccRCC and papillary RCC. Moreover, the extent of ALDH1L1 mRNA level decrease was more pronounced in both histological types of RCC stage III compared with stages I and II (P=0.03). The same was observed for FGD5 gene in ccRCC (P<0.06). |
url |
http://dx.doi.org/10.1155/2014/735292 |
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