Novel markers of gene methylation and expression in breast cancer View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2007-08

AUTHORS

E. B. Kuznetsova, T. V. Kekeeva, S. S. Larin, V. V. Zemlyakova, O. V. Babenko, M. V. Nemtsova, D. V. Zaletayev, V. V. Strelnikov

ABSTRACT

An optimized methylation-sensitive restriction fingerprinting technique was used to search for differentially methylated CpG islands in the tumor genome and detected seven genes subject to abnormal epigenetic regulation in breast cancer: SEMA6B, BIN1, VCPIP1, LAMC3, KCNH2, CACNG4, and PSMF1. For each gene, the rate of promoter methylation and changes in expression were estimated in tumor and morphologically intact paired specimens of breast tissue (N = 100). Significant methylation rates of 38, 18, and 8% were found for SEMA6B, BIN1, and LAMC3, respectively. The genes were not methylated in morphologically intact breast tissue. The expression of SEMA6B, BIN1, VCPIP1, LAMC3, KCNH2, CACNG4, and PSMF1 was decreased in 44–94% of tumor specimens by the real-time RT-PCR assay. The most profound changes in SEMA6B and LAMC3 suggest that these genes can be included in biomarker panels for breast cancer diagnosis. Fine methylation mapping of the most frequently methylated CpG islands (SEMA6B, BIN1, and LAMC3) provides a fundamental basis for developing efficient methylation tests for these genes. More... »

PAGES

562-570

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s0026893307040061

DOI

http://dx.doi.org/10.1134/s0026893307040061

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1012016547


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