Role of a DT-diaphorase mutation in the response of anal canal carcinoma to radiation, 5-fluorouracil, and mitomycin C

Int J Radiat Oncol Biol Phys. 1998 Sep 1;42(2):331-4. doi: 10.1016/s0360-3016(98)00234-x.

Abstract

Purpose: To determine, retrospectively, the status of the bp 609 mutation in the DT-diaphorase gene in anal canal carcinoma patients who have undergone radical radiotherapy with concurrent 5-fluorouracil (5-FU) and mitomycin C (MMC), to determine the relationship of the mutant form of the gene to treatment outcomes.

Methods and materials: Paraffin blocks of pretreatment tumor biopsies were obtained on 49 patients who underwent treatment with curative intent using radiation, infusional 5-FU and bolus MMC from January 1991 to December 1993. DNA was extracted and subjected to polymerase chain reaction (PCR) analysis using primers that encompassed the bp 609 C to T mutation. Restriction endonuclease cleavage with Hinf 1 and gel electrophoresis were used to determine the polymorphism status of each patient.

Results: DNA of 46 patients was successfully amplified. The 46 patients were distributed as follows: 26 (56.5%) C/C-homozygous wildtype, 18 (39%) T/C-heterozygous, and 2 (4.5%) T/T-homozygous mutant. Eleven of 46 patients had suffered treatment failure. The status of the bp 609 polymorphism in this group was 5 (45.5%) C/C, 5 (45.5%) C/T, and 1 (9%) T/T.

Conclusion: In this series, there was not an overrepresentation of the mutant allele in patients with treatment failure, suggesting that the bp 609 alteration is not a strong determinant of treatment outcome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Anus Neoplasms / drug therapy*
  • Anus Neoplasms / enzymology
  • Anus Neoplasms / genetics
  • Anus Neoplasms / radiotherapy*
  • Combined Modality Therapy
  • Fluorouracil / administration & dosage
  • Humans
  • Mitomycin / administration & dosage
  • NAD(P)H Dehydrogenase (Quinone) / genetics*
  • Neoplasm Proteins / genetics*
  • Polymorphism, Genetic
  • Retrospective Studies
  • Treatment Outcome

Substances

  • Neoplasm Proteins
  • Mitomycin
  • NAD(P)H Dehydrogenase (Quinone)
  • Fluorouracil