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

نویسندگان

  • André Lopes Carvalho
  • Alice Chuang
  • Wei-Wen Jiang
  • Juna Lee
  • Shahnaz Begum
  • Luana Poeta
  • Ming Zhao
  • Carmen Jerónimo
  • Rui Henrique
  • Chetan S Nayak
  • Hannah L Park
  • Mariana R O Brait
  • Chunyan Liu
  • Shaoyu Zhou
  • Wayne Koch
  • Vito Michele Fazio
  • Edward Ratovitski
  • Barry Trink
  • William Westra
  • David Sidransky
  • Chul-so Moon
  • Joseph A Califano
چکیده

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.

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عنوان ژورنال:
  • Cancer research

دوره 66 19  شماره 

صفحات  -

تاریخ انتشار 2006