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Secreted frizzled-related protein promotors are hypermethylated in cutaneous squamous carcinoma compared with normal epidermis.

Authors :
Junqin Liang
Xiaojing Kang
Yilinuer Halifu
Xuewen Zeng
Tianbo Jin
Mingxia Zhang
Dong Luo
Yuan Ding
Yunmin Zhou
Yakeya, Buwajier
Abudu, Dilinuer
Xiongming Pu
Liang, Junqin
Kang, Xiaojing
Halifu, Yilinuer
Zeng, Xuewen
Jin, Tianbo
Zhang, Mingxia
Luo, Dong
Ding, Yuan
Source :
BMC Cancer; 9/23/2015, Vol. 15 Issue 1, p1-7, 7p, 4 Charts, 2 Graphs
Publication Year :
2015

Abstract

<bold>Background: </bold>The Wnt signaling pathway is abnormally activated in many human cancers. Secreted frizzled-related proteins (SFRPs) function as negative regulators of Wnt signaling and play an important role in carcinogenesis. SFRP promoter hypermethylation has often been identified in human cancers; however, the precise role of SFRPs in cutaneous squamous cell carcinoma (SCC) is unclear.<bold>Methods: </bold>The methylation status of the SFRP family was analyzed in an age-and sex-matched case-control study, including 40 cutaneous SCC cases and 40 normal controls, using the MassARRAY EpiTYPER system.<bold>Results: </bold>The methylation rate of SFRP1, SFRP2, SFRP4, and SFRP5 promoters was significantly higher in cutaneous SCC tissues than in adjacent tissue and normal skin samples.<bold>Discussion: </bold>Our manuscript mainly discussed the average methylation rate of SFRPs (SFRP1, SFRP2, SFRP4, and SFRP5) promoters are significantly high in tumor tissue samples and the average CpG island methylation rate among different pathological levels of cutaneous SCC between these genes are different.<bold>Conclusions: </bold>Our findings suggest that promoter hypermethylation of SFRPs is associated with the development of carcinoma, and could be a useful tumor marker for cutaneous SCC and other types of cancers. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14712407
Volume :
15
Issue :
1
Database :
Complementary Index
Journal :
BMC Cancer
Publication Type :
Academic Journal
Accession number :
109929241
Full Text :
https://doi.org/10.1186/s12885-015-1650-x