TFAP2E Methylation and Expression Status Does Not Predict Response to 5-FU-based Chemotherapy in Colorectal Cancer


Por: Murcia O, Jover R, Egoavil C, Perez-Carbonell, L, Juarez M, Hernandez E, Rojas E, Alenda C, Balaguer, F, Andreu, M, Llor, X, Castells, A, Boland, C and Goel, A

Publicada: 15 jun 2018
Resumen:
Purpose: A recent study reported that 5 -fluorouracil (5-FU)based dientotherapy is less effective in treating patients with advanced colorectal cancer demonstrating hypermethylation of the TFAP2E gene. The aim of our study was to confirm and validate these findings in large, uniformly treated, wellcharacterized patient cohorts. Experimental Design: Two cohorts of 783 patients with colorectal cancer: 532 from a population-based, multicenter cohort (FPICOLON I) and 251 patients from a clinic-based trial were used to study the effectiveness of TFAP2E methylation and expression as a predictor of response of colorectal cancer patients to 5-FU-based chemotherapy. DNA methylation status of the TFAP2E gene in patients with colorectal cancer was assessed by quantitative hisulfite pyrosequencing analysis. IHC analysis of the TFAP2E protein expression was also performed. Results: Correlation between TFAP2E methylation status and IHC staining was performed in 607 colorectal cancer samples. Among 357 hypermethylated tumors, only 141 (39.6%) exhibited loss of protein expression. Survival was not affected by TFAP2E hypermethylation in stage IV patients PIK 1.21; 95% confidence interval (CI), 0.79-1.87; log-rank P = 0.6]. In stage II-III cases, disease-free survival was not influenced by TEAP2E hypermethylation status in 5-FU-treated (HR, 0.91; 95% Cl, 0.51 1.59; log-rank P = 0.9) as well as in nontreated patients (HR, 88; 95% CI, 0 5 - 1 .54; log-rank P = 0.7). Conclusions: TFAP2E hypemiethylation does nut correlate with loss of its protein expression. Our large, systematic, and comprehensive study indicates that TEAP2E methylation and expression may not play a major role in predicting response to 5-FU-based chemotherapy in patients with colorectal cancer. (C) 2018 AACR.

Filiaciones:
Murcia O:
 Hosp Gen Univ Alicante, Inst Invest Sanitaria ISABIAL, Unidad Gastroenterol, Alicante 12, Alicante 03010, Spain

Jover R:
 Hosp Gen Univ Alicante, Inst Invest Sanitaria ISABIAL, Unidad Gastroenterol, Alicante 12, Alicante 03010, Spain

Egoavil C:
 Hosp Gen Univ Alicante, Inst Invest Sanitaria ISABIAL, Res Unit, Alicante 12, Alicante 03010, Spain

 Hosp Gen Univ Alicante, Inst Invest Sanitaria ISABIAL, Dept Pathol, Alicante 12, Alicante 03010, Spain

Perez-Carbonell, L:
 Baylor Univ, Med Ctr, Ctr Gastrointestinal Res, 3410 Worth St,Suite 610, Dallas, TX 75246 USA

 Baylor Univ, Med Ctr, Ctr Translat Genom & Oncol, Baylor Scott & White Res Inst, 3410 Worth St,Suite 610, Dallas, TX 75246 USA

 Baylor Univ, Med Ctr, Charles A Sammons Canc Ctr, Baylor Res Inst, 3410 Worth St,Suite 610, Dallas, TX 75246 USA

 Baylor Univ, Med Ctr, Sammons Canc Ctr, 3410 Worth St,Suite 610, Dallas, TX 75246 USA

Juarez M:
 Hosp Gen Univ Alicante, Inst Invest Sanitaria ISABIAL, Res Unit, Alicante 12, Alicante 03010, Spain

Hernandez E:
 Hosp Gen Univ Alicante, Inst Invest Sanitaria ISABIAL, Res Unit, Alicante 12, Alicante 03010, Spain

Rojas E:
 Hosp Gen Univ Alicante, Inst Invest Sanitaria ISABIAL, Dept Pathol, Alicante 12, Alicante 03010, Spain

Alenda C:
 Hosp Gen Univ Alicante, Inst Invest Sanitaria ISABIAL, Dept Pathol, Alicante 12, Alicante 03010, Spain

Balaguer, F:
 Univ Barcelona, Hosp Clin, Gastroenterol Dept, IDIBAPS,CIBERehd, Barcelona, Spain

Andreu, M:
 Hosp del Mar, Gastroenterol Dept, Barcelona, Spain

Llor, X:
 Yale Univ, Dept Med, Med Ctr, New Haven, CT 06520 USA

Castells, A:
 Univ Barcelona, Hosp Clin, Gastroenterol Dept, IDIBAPS,CIBERehd, Barcelona, Spain

Boland, C:
 Baylor Univ, Med Ctr, Ctr Gastrointestinal Res, 3410 Worth St,Suite 610, Dallas, TX 75246 USA

 Baylor Univ, Med Ctr, Ctr Translat Genom & Oncol, Baylor Scott & White Res Inst, 3410 Worth St,Suite 610, Dallas, TX 75246 USA

 Baylor Univ, Med Ctr, Charles A Sammons Canc Ctr, Baylor Res Inst, 3410 Worth St,Suite 610, Dallas, TX 75246 USA

 Baylor Univ, Med Ctr, Sammons Canc Ctr, 3410 Worth St,Suite 610, Dallas, TX 75246 USA

Goel, A:
 Baylor Univ, Med Ctr, Ctr Gastrointestinal Res, 3410 Worth St,Suite 610, Dallas, TX 75246 USA

 Baylor Univ, Med Ctr, Ctr Translat Genom & Oncol, Baylor Scott & White Res Inst, 3410 Worth St,Suite 610, Dallas, TX 75246 USA

 Baylor Univ, Med Ctr, Charles A Sammons Canc Ctr, Baylor Res Inst, 3410 Worth St,Suite 610, Dallas, TX 75246 USA

 Baylor Univ, Med Ctr, Sammons Canc Ctr, 3410 Worth St,Suite 610, Dallas, TX 75246 USA
ISSN: 10780432





CLINICAL CANCER RESEARCH
Editorial
AMER ASSOC CANCER RESEARCH, 615 CHESTNUT ST, 17TH FLOOR, PHILADELPHIA, PA 19106-4404 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 24 Número: 12
Páginas: 2820-2827
WOS Id: 000435462700013
ID de PubMed: 29535127

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