Thymidylate synthase expression in oral squamous cell carcinoma predicts response to S-1

Oncol Rep. 2006 Jun;15(6):1417-23.

Abstract

The purpose of this research was to evaluate the predictive value of expression of thymidylate synthase (TS), dihydropyrimidine dehydrogenase (DPD), thymidine phosphorylase (TP), or orotate phosphoribosyltransferase (OPRT) genes for response to S-1. Twenty-five patients with oral squamous cell carcinoma (OSCC) received S-1 80 mg/m2/day. Pretreatment tumor biopsies were analyzed for TS, DPD, TP or OPRT mRNA expression by real-time reverse transcription-PCR. TS protein expression was evaluated by immunohistochemistry using a polyclonal TS antibody. Twenty-five patients were evaluable for response and gene expression. Six of the 25 (24%) achieved complete remission and 4 of the 25 (16%) had a partial response. Median TS/beta-actin was 2.51 (range 0.98-7.07). Median TS/beta-actin was 1.26 in responding patients and 3.43 in non-responders (P=0.0001). Ten of 11 patients with TS/beta-actin <1.80 and 0 of 15 with higher values responded (P<0.0001). Overall survival was 29.7 months in patients with TS/beta-actin <1.80 and 41.7 months in patients with higher values (P=0.0013). No correlations were seen between expression of DPD, TP or OPRT mRNA and response or survival. Weak TS staining was seen in 6 of 25 tumors evaluable for immunohistochemistry, including 5 responders. All 4 of the patients with both weak staining and TS/beta-actin <1.80 responded. High TS mRNA expression predicts non-response to S-1. On the other hand, high levels of DPD or TP mRNA and low levels of OPRT mRNA are not associated with S-1 resistance. TS mRNA expression is considered to be a useful prognostic factor in OSCC patients with S-1 single-agent therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Carcinoma, Squamous Cell / drug therapy*
  • Carcinoma, Squamous Cell / enzymology*
  • Carcinoma, Squamous Cell / genetics
  • Dihydrouracil Dehydrogenase (NADP) / biosynthesis
  • Dihydrouracil Dehydrogenase (NADP) / genetics
  • Dihydrouracil Dehydrogenase (NADP) / metabolism
  • Drug Combinations
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mouth Neoplasms / drug therapy*
  • Mouth Neoplasms / enzymology*
  • Mouth Neoplasms / genetics
  • Multienzyme Complexes / biosynthesis
  • Multienzyme Complexes / genetics
  • Multienzyme Complexes / metabolism
  • Orotate Phosphoribosyltransferase / biosynthesis
  • Orotate Phosphoribosyltransferase / genetics
  • Orotate Phosphoribosyltransferase / metabolism
  • Orotidine-5'-Phosphate Decarboxylase / biosynthesis
  • Orotidine-5'-Phosphate Decarboxylase / genetics
  • Orotidine-5'-Phosphate Decarboxylase / metabolism
  • Oxonic Acid / therapeutic use*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Tegafur / therapeutic use*
  • Thymidine Phosphorylase / biosynthesis
  • Thymidine Phosphorylase / genetics
  • Thymidine Phosphorylase / metabolism
  • Thymidylate Synthase / biosynthesis*
  • Thymidylate Synthase / genetics
  • Thymidylate Synthase / metabolism

Substances

  • Drug Combinations
  • Multienzyme Complexes
  • RNA, Messenger
  • S 1 (combination)
  • Tegafur
  • Oxonic Acid
  • uridine 5'-monophosphate synthase
  • Dihydrouracil Dehydrogenase (NADP)
  • Thymidylate Synthase
  • Orotate Phosphoribosyltransferase
  • Thymidine Phosphorylase
  • Orotidine-5'-Phosphate Decarboxylase