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PMID: 17018594 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Deleted in colorectal cancer is a putative conditional tumor-suppressor gene inactivated by promoter hypermethylation in head and neck squamous cell carcinoma.

Cancer research ·Vol. 66 ·No. 19 ·2006-10-01 ·页码 9401-7

Carvalho AL, Chuang A, Jiang WW, Lee J, Begum S, Poeta L, Zhao M, Jerónimo C, Henrique R, Nayak CS, Park HL, Brait MR, Liu C, Zhou S, Koch W, Fazio VM, Ratovitski E, Trink B, Westra W, Sidransky D, Moon CS, Califano JA

Abstract

Deleted in colorectal cancer (DCC) is a candidate tumor-suppressor gene located at chromosome 18q21. However, DCC gene was found to have few somatic mutations and the heterozygous mice (DCC(+/-)) showed a similar frequency of tumor formation compared with the wild-type mice (DCC(+/+)). Recently, DCC came back to the spotlight as a better understating of its function and relationship with its ligand (netrin-1) had shown that DCC may act as a conditional tumor-suppressor gene. We evaluated hypermethylation as a mechanism for DCC inactivation in head and neck squamous cell carcinoma (HNSCC). DCC promoter region hypermethylation was found in 75% of primary HNSCC. There was a significant correlation between DCC promoter region hypermethylation and DCC expression (assessed by immunohistochemistry; P = 0.021). DCC nonexpressing HNSCC cell lines JHU-O12 and JHU-O19 with baseline hypermethylation of the DCC promoter were treated with 5-aza-2'-deoxycytidine (a demethylating agent) and reexpression of DCC was noted. Transfection of DCC into DCC-negative HNSCC cell lines resulted in complete abrogation of growth in all cell lines, whereas additional cotransfection of netrin-1 resulted in rescue of DCC-mediated growth inhibition. These results suggest that DCC is a putative conditional tumor-suppressor gene that is epigenetically inactivated by promoter hypermethylation in a majority of HNSCC.

MeSH 主题词
Carcinoma, Squamous Cell/genetics,pathology Cell Line, Tumor CpG Islands/genetics DCC Receptor DNA Methylation DNA, Neoplasm/chemistry,genetics Gene Expression Regulation, Neoplastic Genes, DCC Head and Neck Neoplasms/genetics,pathology Humans Loss of Heterozygosity Neoplasm Proteins/biosynthesis,deficiency,genetics,physiology Nerve Growth Factors/genetics,physiology Netrin-1 Promoter Regions, Genetic/genetics Receptors, Cell Surface/biosynthesis,deficiency,physiology Transfection Tumor Suppressor Proteins/biosynthesis,deficiency,genetics,physiology
化学物质
DCC Receptor DCC protein, human DNA, Neoplasm NTN1 protein, human Neoplasm Proteins Nerve Growth Factors Ntn1 protein, mouse Receptors, Cell Surface Tumor Suppressor Proteins Netrin-1
作者与单位
共 22 位作者,点击展开单位 / ORCID
Carvalho André Lopes
Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins Medical Institutions, Baltimore, MD 21287-0910, USA.
Chuang Alice
Jiang Wei-Wen
Lee Juna
Begum Shahnaz
Poeta Luana
Zhao Ming
Jerónimo Carmen
Henrique Rui
Nayak Chetan S
Park Hannah L
Brait Mariana R O
Liu Chunyan
Zhou Shaoyu
Koch Wayne
Fazio Vito Michele
Ratovitski Edward
Trink Barry
Westra William
Sidransky David
Moon Chul-so
Califano Joseph A
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
1538-7445
Published
2006-10-01
页码
9401-7
Language
English
Country/Region
United States
NLM ID
2984705R
基金资助
NIDCR NIH HHS · 1R01DE015939-01 · United States
NCI NIH HHS · P50 CA96784 · United States
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