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

BACKGROUND: 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; ho...

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Autores principales: Liang, Junqin, Kang, Xiaojing, Halifu, Yilinuer, Zeng, Xuewen, Jin, Tianbo, Zhang, Mingxia, Luo, Dong, Ding, Yuan, Zhou, Yunmin, Yakeya, Buwajier, Abudu, Dilinuer, Pu, Xiongming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4579584/
https://www.ncbi.nlm.nih.gov/pubmed/26394929
http://dx.doi.org/10.1186/s12885-015-1650-x
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author Liang, Junqin
Kang, Xiaojing
Halifu, Yilinuer
Zeng, Xuewen
Jin, Tianbo
Zhang, Mingxia
Luo, Dong
Ding, Yuan
Zhou, Yunmin
Yakeya, Buwajier
Abudu, Dilinuer
Pu, Xiongming
author_facet Liang, Junqin
Kang, Xiaojing
Halifu, Yilinuer
Zeng, Xuewen
Jin, Tianbo
Zhang, Mingxia
Luo, Dong
Ding, Yuan
Zhou, Yunmin
Yakeya, Buwajier
Abudu, Dilinuer
Pu, Xiongming
author_sort Liang, Junqin
collection PubMed
description BACKGROUND: 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. METHODS: 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. RESULTS: 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. DISCUSSION: 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. CONCLUSIONS: 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.
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spelling pubmed-45795842015-09-24 Secreted frizzled-related protein promotors are hypermethylated in cutaneous squamous carcinoma compared with normal epidermis Liang, Junqin Kang, Xiaojing Halifu, Yilinuer Zeng, Xuewen Jin, Tianbo Zhang, Mingxia Luo, Dong Ding, Yuan Zhou, Yunmin Yakeya, Buwajier Abudu, Dilinuer Pu, Xiongming BMC Cancer Research Article BACKGROUND: 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. METHODS: 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. RESULTS: 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. DISCUSSION: 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. CONCLUSIONS: 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. BioMed Central 2015-09-22 /pmc/articles/PMC4579584/ /pubmed/26394929 http://dx.doi.org/10.1186/s12885-015-1650-x Text en © Liang et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Liang, Junqin
Kang, Xiaojing
Halifu, Yilinuer
Zeng, Xuewen
Jin, Tianbo
Zhang, Mingxia
Luo, Dong
Ding, Yuan
Zhou, Yunmin
Yakeya, Buwajier
Abudu, Dilinuer
Pu, Xiongming
Secreted frizzled-related protein promotors are hypermethylated in cutaneous squamous carcinoma compared with normal epidermis
title Secreted frizzled-related protein promotors are hypermethylated in cutaneous squamous carcinoma compared with normal epidermis
title_full Secreted frizzled-related protein promotors are hypermethylated in cutaneous squamous carcinoma compared with normal epidermis
title_fullStr Secreted frizzled-related protein promotors are hypermethylated in cutaneous squamous carcinoma compared with normal epidermis
title_full_unstemmed Secreted frizzled-related protein promotors are hypermethylated in cutaneous squamous carcinoma compared with normal epidermis
title_short Secreted frizzled-related protein promotors are hypermethylated in cutaneous squamous carcinoma compared with normal epidermis
title_sort secreted frizzled-related protein promotors are hypermethylated in cutaneous squamous carcinoma compared with normal epidermis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4579584/
https://www.ncbi.nlm.nih.gov/pubmed/26394929
http://dx.doi.org/10.1186/s12885-015-1650-x
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