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Published in: BMC Cancer 1/2014

Open Access 01-12-2014 | Research article

Decreased GATA5 mRNA expression associates with CpG island methylation and shortened recurrence-free survival in clear cell renal cell carcinoma

Authors: Inga Peters, Natalia Dubrowinskaja, Michael Kogosov, Mahmoud Abbas, Jörg Hennenlotter, Christoph von Klot, Axel S Merseburger, Arnulf Stenzl, Ralph Scherer, Markus A Kuczyk, Jürgen Serth

Published in: BMC Cancer | Issue 1/2014

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Abstract

Background

GATA-5, a zinc-finger transcription factor and member of the GATA family proteins 1–6, is known to be involved in cellular differentiation. We recently found that tumor-specific hypermethylation of the GATA5 CpG island (CGI) occurs in renal cell carcinoma (RCC) and is associated with an adverse clinical outcome. In this study, we investigated whether epigenetic GATA5 alterations may result in changes in GATA5 mRNA expression levels and correlate with the observed prognostic impact of epigenetic changes in GATA5 in RCC.

Methods

Quantitative real-time reverse-transcribed polymerase chain reaction was applied to measure relative GATA5 mRNA expression levels in 135 kidney tissue samples, including 77 clear cell RCC (ccRCC) tissues and 58 paired adjacent normal renal tissue samples. Relative GATA5 expression levels were determined using the ΔΔCt method and detection of three endogenous control genes then compared to previously measured values of relative methylation.

Results

The mean relative GATA5 mRNA expression level exhibited an approximately 31-fold reduction in tumor specimens compared with corresponding normal tissues (p < 0.001, paired t-test). Decreased GATA5 mRNA expression was inversely correlated with increased GATA5 CGI methylation (p < 0.001) and was associated with shortened recurrence-free survival in ccRCC patients (p = 0.023, hazard ratio = 0.25).

Conclusion

GATA5 mRNA expression is decreased in ccRCC, likely due to gene silencing by methylation of the GATA5 CGI. Moreover, reduced GATA5 mRNA levels were associated with a poor clinical outcome, indicating a possible role of GATA5 for the development of aggressive ccRCC phenotypes.
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Literature
1.
go back to reference Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D: Global cancer statistics. CA Cancer J Clin. 2011, 61 (2): 69-90. 10.3322/caac.20107.CrossRefPubMed Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D: Global cancer statistics. CA Cancer J Clin. 2011, 61 (2): 69-90. 10.3322/caac.20107.CrossRefPubMed
2.
go back to reference Morrisey EE, Ip HS, Tang Z, Lu MM, Parmacek MS: GATA-5: a transcriptional activator expressed in a novel temporally and spatially-restricted pattern during embryonic development. Dev Biol. 1997, 183 (1): 21-36. 10.1006/dbio.1996.8485.CrossRefPubMed Morrisey EE, Ip HS, Tang Z, Lu MM, Parmacek MS: GATA-5: a transcriptional activator expressed in a novel temporally and spatially-restricted pattern during embryonic development. Dev Biol. 1997, 183 (1): 21-36. 10.1006/dbio.1996.8485.CrossRefPubMed
3.
go back to reference Gao X, Sedgwick T, Shi YB, Evans T: Distinct functions are implicated for the GATA-4, -5, and −6 transcription factors in the regulation of intestine epithelial cell differentiation. Mol Cell Biol. 1998, 18 (5): 2901-2911.CrossRefPubMedPubMedCentral Gao X, Sedgwick T, Shi YB, Evans T: Distinct functions are implicated for the GATA-4, -5, and −6 transcription factors in the regulation of intestine epithelial cell differentiation. Mol Cell Biol. 1998, 18 (5): 2901-2911.CrossRefPubMedPubMedCentral
4.
go back to reference Ren CY, Akiyama Y, Miyake S, Yuasa Y: Transcription factor GATA-5 selectively up-regulates mucin gene expression. J Cancer Res Clin Oncol. 2004, 130 (5): 245-252. 10.1007/s00432-003-0537-4.CrossRefPubMed Ren CY, Akiyama Y, Miyake S, Yuasa Y: Transcription factor GATA-5 selectively up-regulates mucin gene expression. J Cancer Res Clin Oncol. 2004, 130 (5): 245-252. 10.1007/s00432-003-0537-4.CrossRefPubMed
5.
go back to reference Kiela PR, LeSueur J, Collins JF, Ghishan FK: Transcriptional regulation of the rat NHE3 gene. Functional interactions between GATA-5 and Sp family transcription factors. J Biol Chem. 2003, 278 (8): 5659-5668. 10.1074/jbc.M209473200.CrossRefPubMed Kiela PR, LeSueur J, Collins JF, Ghishan FK: Transcriptional regulation of the rat NHE3 gene. Functional interactions between GATA-5 and Sp family transcription factors. J Biol Chem. 2003, 278 (8): 5659-5668. 10.1074/jbc.M209473200.CrossRefPubMed
6.
go back to reference Akiyama Y, Watkins N, Suzuki H, Jair K-W, van Engeland M, Esteller M, Sakai H, Ren C-Y, Yuasa Y, Herman JG, et al: GATA-4 and GATA-5 transcription factor genes and potential downstream antitumor target genes are epigenetically silenced in colorectal and gastric cancer. Mol Cell Biol. 2003, 23 (23): 8429-8439. 10.1128/MCB.23.23.8429-8439.2003.CrossRefPubMedPubMedCentral Akiyama Y, Watkins N, Suzuki H, Jair K-W, van Engeland M, Esteller M, Sakai H, Ren C-Y, Yuasa Y, Herman JG, et al: GATA-4 and GATA-5 transcription factor genes and potential downstream antitumor target genes are epigenetically silenced in colorectal and gastric cancer. Mol Cell Biol. 2003, 23 (23): 8429-8439. 10.1128/MCB.23.23.8429-8439.2003.CrossRefPubMedPubMedCentral
7.
go back to reference Wakana K, Akiyama Y, Aso T, Yuasa Y: Involvement of GATA-4/-5 transcription factors in ovarian carcinogenesis. Cancer Lett. 2006, 241 (2): 281-288. 10.1016/j.canlet.2005.10.039.CrossRefPubMed Wakana K, Akiyama Y, Aso T, Yuasa Y: Involvement of GATA-4/-5 transcription factors in ovarian carcinogenesis. Cancer Lett. 2006, 241 (2): 281-288. 10.1016/j.canlet.2005.10.039.CrossRefPubMed
8.
go back to reference Guo M, Akiyama Y, House MG, Hooker CM, Heath E, Gabrielson E, Yang SC, Han Y, Baylin SB, Herman JG, et al: Hypermethylation of the GATA genes in lung cancer. Clin Cancer Res. 2004, 10 (23): 7917-7924. 10.1158/1078-0432.CCR-04-1140.CrossRefPubMed Guo M, Akiyama Y, House MG, Hooker CM, Heath E, Gabrielson E, Yang SC, Han Y, Baylin SB, Herman JG, et al: Hypermethylation of the GATA genes in lung cancer. Clin Cancer Res. 2004, 10 (23): 7917-7924. 10.1158/1078-0432.CCR-04-1140.CrossRefPubMed
9.
go back to reference Guo M, House MG, Akiyama Y, Qi Y, Capagna D, Harmon J, Baylin SB, Brock MV, Herman JG: Hypermethylation of the GATA gene family in esophageal cancer. Int J Cancer. 2006, 119 (9): 2078-2083. 10.1002/ijc.22092.CrossRefPubMed Guo M, House MG, Akiyama Y, Qi Y, Capagna D, Harmon J, Baylin SB, Brock MV, Herman JG: Hypermethylation of the GATA gene family in esophageal cancer. Int J Cancer. 2006, 119 (9): 2078-2083. 10.1002/ijc.22092.CrossRefPubMed
10.
go back to reference Fu B, Guo M, Wang S, Campagna D, Luo M, Herman JG, Iacobuzio-Donahue CA: Evaluation of GATA-4 and GATA-5 methylation profiles in human pancreatic cancers indicate promoter methylation patterns distinct from other human tumor types. Cancer Biol Ther. 2007, 6 (10): 1546-1552. 10.4161/cbt.6.10.4708.CrossRefPubMed Fu B, Guo M, Wang S, Campagna D, Luo M, Herman JG, Iacobuzio-Donahue CA: Evaluation of GATA-4 and GATA-5 methylation profiles in human pancreatic cancers indicate promoter methylation patterns distinct from other human tumor types. Cancer Biol Ther. 2007, 6 (10): 1546-1552. 10.4161/cbt.6.10.4708.CrossRefPubMed
11.
go back to reference Peters I, Eggers H, Atschekzei F, Hennenlotter J, Waalkes S, Trankenschuh W, Grosshennig A, Merseburger AS, Stenzl A, Kuczyk MA, et al: GATA5 CpG island methylation in renal cell cancer: a potential biomarker for metastasis and disease progression. BJU Int. 2012, 110 (2 Pt 2): E144-E152.CrossRefPubMed Peters I, Eggers H, Atschekzei F, Hennenlotter J, Waalkes S, Trankenschuh W, Grosshennig A, Merseburger AS, Stenzl A, Kuczyk MA, et al: GATA5 CpG island methylation in renal cell cancer: a potential biomarker for metastasis and disease progression. BJU Int. 2012, 110 (2 Pt 2): E144-E152.CrossRefPubMed
12.
go back to reference Waalkes S, Atschekzei F, Kramer MW, Hennenlotter J, Vetter G, Becker JU, Stenzl A, Merseburger AS, Schrader AJ, Kuczyk MA, et al: Fibronectin 1 mRNA expression correlates with advanced disease in renal cancer. BMC Cancer. 2010, 10: 503-10.1186/1471-2407-10-503.CrossRefPubMedPubMedCentral Waalkes S, Atschekzei F, Kramer MW, Hennenlotter J, Vetter G, Becker JU, Stenzl A, Merseburger AS, Schrader AJ, Kuczyk MA, et al: Fibronectin 1 mRNA expression correlates with advanced disease in renal cancer. BMC Cancer. 2010, 10: 503-10.1186/1471-2407-10-503.CrossRefPubMedPubMedCentral
13.
go back to reference Livak KJ, Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) Method. Methods. 2001, 25 (4): 402-408. 10.1006/meth.2001.1262.CrossRefPubMed Livak KJ, Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) Method. Methods. 2001, 25 (4): 402-408. 10.1006/meth.2001.1262.CrossRefPubMed
14.
go back to reference Schmittgen TD, Livak KJ: Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc. 2008, 3 (6): 1101-1108. 10.1038/nprot.2008.73.CrossRefPubMed Schmittgen TD, Livak KJ: Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc. 2008, 3 (6): 1101-1108. 10.1038/nprot.2008.73.CrossRefPubMed
Metadata
Title
Decreased GATA5 mRNA expression associates with CpG island methylation and shortened recurrence-free survival in clear cell renal cell carcinoma
Authors
Inga Peters
Natalia Dubrowinskaja
Michael Kogosov
Mahmoud Abbas
Jörg Hennenlotter
Christoph von Klot
Axel S Merseburger
Arnulf Stenzl
Ralph Scherer
Markus A Kuczyk
Jürgen Serth
Publication date
01-12-2014
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2014
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/1471-2407-14-101

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