Identification of 5 novel genes methylated in breast and other epithelial cancers

Hill, Victoria K., Hesson, Luke B., Dansranjavin, Temuujin, Dallol, Ashraf, Bieche, Ivan, Vacher, Sophie, Tommasi, Stella, Dobbins, Timothy, Gentle, Dean, Euhus, David, Lewis, Cheryl, Dammann, Reinhard, Ward, Robyn L., Minna, John, Maher, Eammon R., Pfeifer, Gerd P. and Latif, Farida (2010) Identification of 5 novel genes methylated in breast and other epithelial cancers. Molecular Cancer, 9 . doi:10.1186/1476-4598-9-51

Author Hill, Victoria K.
Hesson, Luke B.
Dansranjavin, Temuujin
Dallol, Ashraf
Bieche, Ivan
Vacher, Sophie
Tommasi, Stella
Dobbins, Timothy
Gentle, Dean
Euhus, David
Lewis, Cheryl
Dammann, Reinhard
Ward, Robyn L.
Minna, John
Maher, Eammon R.
Pfeifer, Gerd P.
Latif, Farida
Title Identification of 5 novel genes methylated in breast and other epithelial cancers
Journal name Molecular Cancer   Check publisher's open access policy
ISSN 1476-4598
Publication date 2010-03-05
Year available 2010
Sub-type Article (original research)
DOI 10.1186/1476-4598-9-51
Open Access Status DOI
Volume 9
Total pages 13
Place of publication London, United Kingdom
Publisher BioMed Central
Language eng
Formatted abstract
Background: There are several high throughput approaches to identify methylated genes in cancer. We utilized one such recently developed approach, MIRA (methylated-CpG island recovery assay) combined with CpG island arrays to identify novel genes that are epigenetically inactivated in breast cancer.

Results: Using this approach we identified numerous CpG islands that demonstrated aberrant DNA methylation in breast cancer cell lines. Using a combination of COBRA and sequencing of bisulphite modified DNA, we confirmed 5 novel genes frequently methylated in breast tumours; EMILIN2, SALL1, DBC1, FBLN2 and CIDE-A. Methylation frequencies ranged from between 25% and 63% in primary breast tumours, whilst matched normal breast tissue DNA was either unmethylated or demonstrated a much lower frequency of methylation compared to malignant breast tissue DNA. Furthermore expression of the above 5 genes was shown to be restored following treatment with a demethylating agent in methylated breast cancer cell lines. We have expanded this analysis across three other common epithelial cancers (lung, colorectal, prostate). We demonstrate that the above genes show varying levels of methylation in these cancers. Lastly and most importantly methylation of EMILIN2 was associated with poorer clinical outcome in breast cancer and was strongly associated with estrogen receptor as well as progesterone receptor positive breast cancers.

Conclusion: The combination of the MIRA assay with CpG island arrays is a very useful technique for identifying epigenetically inactivated genes in cancer genomes and can provide molecular markers for early cancer diagnosis, prognosis and epigenetic therapy.
Keyword Biochemistry & Molecular Biology
Biochemistry & Molecular Biology
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status UQ

Document type: Journal Article
Sub-type: Article (original research)
Collections: Office of the Vice-Chancellor
School of Medicine Publications
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Citation counts: TR Web of Science Citation Count  Cited 42 times in Thomson Reuters Web of Science Article | Citations
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