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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Main Authors: 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
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2014/735292
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spelling 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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