Differential expression of selected histone modifier genes in human solid cancers.

BACKGROUND: Post-translational modification of histones resulting in chromatin remodelling plays a key role in the regulation of gene expression. Here we report characteristic patterns of expression of 12 members of 3 classes of chromatin modifier genes in 6 different cancer types: histone acetyltr...

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Main Authors: Ozdağ, H, Teschendorff, A, Ahmed, A, Hyland, S, Blenkiron, C, Bobrow, L, Veerakumarasivam, A, Burtt, G, Subkhankulova, T, Arends, M, Collins, V, Bowtell, D, Kouzarides, T, Brenton, J, Caldas, C
Format: Journal article
Language:English
Published: BioMed Central 2006
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author Ozdağ, H
Teschendorff, A
Ahmed, A
Hyland, S
Blenkiron, C
Bobrow, L
Veerakumarasivam, A
Burtt, G
Subkhankulova, T
Arends, M
Collins, V
Bowtell, D
Kouzarides, T
Brenton, J
Caldas, C
author_facet Ozdağ, H
Teschendorff, A
Ahmed, A
Hyland, S
Blenkiron, C
Bobrow, L
Veerakumarasivam, A
Burtt, G
Subkhankulova, T
Arends, M
Collins, V
Bowtell, D
Kouzarides, T
Brenton, J
Caldas, C
author_sort Ozdağ, H
collection OXFORD
description BACKGROUND: Post-translational modification of histones resulting in chromatin remodelling plays a key role in the regulation of gene expression. Here we report characteristic patterns of expression of 12 members of 3 classes of chromatin modifier genes in 6 different cancer types: histone acetyltransferases (HATs)- EP300, CREBBP, and PCAF; histone deacetylases (HDACs)- HDAC1, HDAC2, HDAC4, HDAC5, HDAC7A, and SIRT1; and histone methyltransferases (HMTs)- SUV39H1and SUV39H2. Expression of each gene in 225 samples (135 primary tumours, 47 cancer cell lines, and 43 normal tissues) was analysedby QRT-PCR, normalized with 8 housekeeping genes, and given as a ratio by comparison with a universal reference RNA. RESULTS: This involved a total of 13,000 PCR assays allowing for rigorous analysis by fitting a linear regression model to the data. Mutation analysis of HDAC1, HDAC2, SUV39H1, and SUV39H2 revealed only two out of 181 cancer samples (both cell lines) with significant coding-sequence alterations. Supervised analysis and Independent Component Analysis showed that expression of many of these genes was able to discriminate tumour samples from their normal counterparts. Clustering based on the normalized expression ratios of the 12 genes also showed that most samples were grouped according to tissue type. Using a linear discriminant classifier and internal cross-validation revealed that with as few as 5 of the 12 genes, SIRT1, CREBBP, HDAC7A, HDAC5 and PCAF, most samples were correctly assigned. CONCLUSION: The expression patterns of HATs, HDACs, and HMTs suggest these genes are important in neoplastic transformation and have characteristic patterns of expression depending on tissue of origin, with implications for potential clinical application.
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spelling oxford-uuid:4245e967-e4c2-4a17-a2fc-22da16d30de82022-03-26T14:48:33ZDifferential expression of selected histone modifier genes in human solid cancers.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:4245e967-e4c2-4a17-a2fc-22da16d30de8EnglishSymplectic Elements at OxfordBioMed Central2006Ozdağ, HTeschendorff, AAhmed, AHyland, SBlenkiron, CBobrow, LVeerakumarasivam, ABurtt, GSubkhankulova, TArends, MCollins, VBowtell, DKouzarides, TBrenton, JCaldas, C BACKGROUND: Post-translational modification of histones resulting in chromatin remodelling plays a key role in the regulation of gene expression. Here we report characteristic patterns of expression of 12 members of 3 classes of chromatin modifier genes in 6 different cancer types: histone acetyltransferases (HATs)- EP300, CREBBP, and PCAF; histone deacetylases (HDACs)- HDAC1, HDAC2, HDAC4, HDAC5, HDAC7A, and SIRT1; and histone methyltransferases (HMTs)- SUV39H1and SUV39H2. Expression of each gene in 225 samples (135 primary tumours, 47 cancer cell lines, and 43 normal tissues) was analysedby QRT-PCR, normalized with 8 housekeeping genes, and given as a ratio by comparison with a universal reference RNA. RESULTS: This involved a total of 13,000 PCR assays allowing for rigorous analysis by fitting a linear regression model to the data. Mutation analysis of HDAC1, HDAC2, SUV39H1, and SUV39H2 revealed only two out of 181 cancer samples (both cell lines) with significant coding-sequence alterations. Supervised analysis and Independent Component Analysis showed that expression of many of these genes was able to discriminate tumour samples from their normal counterparts. Clustering based on the normalized expression ratios of the 12 genes also showed that most samples were grouped according to tissue type. Using a linear discriminant classifier and internal cross-validation revealed that with as few as 5 of the 12 genes, SIRT1, CREBBP, HDAC7A, HDAC5 and PCAF, most samples were correctly assigned. CONCLUSION: The expression patterns of HATs, HDACs, and HMTs suggest these genes are important in neoplastic transformation and have characteristic patterns of expression depending on tissue of origin, with implications for potential clinical application.
spellingShingle Ozdağ, H
Teschendorff, A
Ahmed, A
Hyland, S
Blenkiron, C
Bobrow, L
Veerakumarasivam, A
Burtt, G
Subkhankulova, T
Arends, M
Collins, V
Bowtell, D
Kouzarides, T
Brenton, J
Caldas, C
Differential expression of selected histone modifier genes in human solid cancers.
title Differential expression of selected histone modifier genes in human solid cancers.
title_full Differential expression of selected histone modifier genes in human solid cancers.
title_fullStr Differential expression of selected histone modifier genes in human solid cancers.
title_full_unstemmed Differential expression of selected histone modifier genes in human solid cancers.
title_short Differential expression of selected histone modifier genes in human solid cancers.
title_sort differential expression of selected histone modifier genes in human solid cancers
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