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Impact of the expression of thymidylate synthase and dihydropyrimidine dehydrogenase genes on survival in stage II/III gastric cancer

BACKGROUND: The efficacy of 5-fluorouracil (5FU)-based therapy, which remains the cornerstone of gastrointestinal cancer treatment, depends upon the expression of enzymes involved in pyrimidine metabolism, including thymidylate synthase (TS), dihydropyrimidine dehydrogenase (DPD), thymidine phosphor...

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Autores principales: Sasako, Mitsuru, Terashima, Masanori, Ichikawa, Wataru, Ochiai, Atsushi, Kitada, Koji, Kurahashi, Issei, Sakuramoto, Shinichi, Katai, Hitoshi, Sano, Takeshi, Imamura, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511074/
https://www.ncbi.nlm.nih.gov/pubmed/25112781
http://dx.doi.org/10.1007/s10120-014-0413-8
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author Sasako, Mitsuru
Terashima, Masanori
Ichikawa, Wataru
Ochiai, Atsushi
Kitada, Koji
Kurahashi, Issei
Sakuramoto, Shinichi
Katai, Hitoshi
Sano, Takeshi
Imamura, Hiroshi
author_facet Sasako, Mitsuru
Terashima, Masanori
Ichikawa, Wataru
Ochiai, Atsushi
Kitada, Koji
Kurahashi, Issei
Sakuramoto, Shinichi
Katai, Hitoshi
Sano, Takeshi
Imamura, Hiroshi
author_sort Sasako, Mitsuru
collection PubMed
description BACKGROUND: The efficacy of 5-fluorouracil (5FU)-based therapy, which remains the cornerstone of gastrointestinal cancer treatment, depends upon the expression of enzymes involved in pyrimidine metabolism, including thymidylate synthase (TS), dihydropyrimidine dehydrogenase (DPD), thymidine phosphorylase (TP), and orotate phosphoribosyltransferase (OPRT). We analyzed the expression of these genes in patients enrolled in the Adjuvant Chemotherapy Trial of S-1 for Gastric Cancer (ACTS-GC) and their possible roles as biomarkers for treatment outcomes. METHODS: Formalin-fixed, paraffin-embedded specimens were available for 829 of a total of 1,059 (78.3 %) patients. TS, DPD, TP, and OPRT expression was measured by RT-PCR in manually microdissected tumor specimens and normalized to the reference gene, β-actin. The expression level of each gene was categorized as low or high using cutoffs at the 33.3rd, 50th, or 66.7th percentiles. RESULTS: The hazard ratio (HR) for overall survival (OS) after S-1 treatment versus surgery alone was significantly lower in high (>66.7th percentile; HR = 0.370; 95 % CI 0.221–0.619) compared to low (<66.7th percentile; HR = 0.757; 95 % CI 0.563–1.018) TS expression groups (P = 0.015). Similarly, the HR for OS after S-1 therapy versus surgery alone was significantly lower in high (>33.3rd percentile; HR = 0.520, 95 % CI 0.376–0.720) compared to low (<33.3rd percentile; HR = 0.848, 95 % CI 0.563–1.276) DPD expression groups (P = 0.065). There was no interaction between TP or OPRT expression and OS. CONCLUSIONS: This large biomarker study showed that high TS and DPD gene expression in tumors was associated with enhanced benefit from postoperative adjuvant S-1 treatment in gastric cancer. There was no interaction between TP and OPRT expression and S-1 treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10120-014-0413-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-45110742015-07-23 Impact of the expression of thymidylate synthase and dihydropyrimidine dehydrogenase genes on survival in stage II/III gastric cancer Sasako, Mitsuru Terashima, Masanori Ichikawa, Wataru Ochiai, Atsushi Kitada, Koji Kurahashi, Issei Sakuramoto, Shinichi Katai, Hitoshi Sano, Takeshi Imamura, Hiroshi Gastric Cancer Original Article BACKGROUND: The efficacy of 5-fluorouracil (5FU)-based therapy, which remains the cornerstone of gastrointestinal cancer treatment, depends upon the expression of enzymes involved in pyrimidine metabolism, including thymidylate synthase (TS), dihydropyrimidine dehydrogenase (DPD), thymidine phosphorylase (TP), and orotate phosphoribosyltransferase (OPRT). We analyzed the expression of these genes in patients enrolled in the Adjuvant Chemotherapy Trial of S-1 for Gastric Cancer (ACTS-GC) and their possible roles as biomarkers for treatment outcomes. METHODS: Formalin-fixed, paraffin-embedded specimens were available for 829 of a total of 1,059 (78.3 %) patients. TS, DPD, TP, and OPRT expression was measured by RT-PCR in manually microdissected tumor specimens and normalized to the reference gene, β-actin. The expression level of each gene was categorized as low or high using cutoffs at the 33.3rd, 50th, or 66.7th percentiles. RESULTS: The hazard ratio (HR) for overall survival (OS) after S-1 treatment versus surgery alone was significantly lower in high (>66.7th percentile; HR = 0.370; 95 % CI 0.221–0.619) compared to low (<66.7th percentile; HR = 0.757; 95 % CI 0.563–1.018) TS expression groups (P = 0.015). Similarly, the HR for OS after S-1 therapy versus surgery alone was significantly lower in high (>33.3rd percentile; HR = 0.520, 95 % CI 0.376–0.720) compared to low (<33.3rd percentile; HR = 0.848, 95 % CI 0.563–1.276) DPD expression groups (P = 0.065). There was no interaction between TP or OPRT expression and OS. CONCLUSIONS: This large biomarker study showed that high TS and DPD gene expression in tumors was associated with enhanced benefit from postoperative adjuvant S-1 treatment in gastric cancer. There was no interaction between TP and OPRT expression and S-1 treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10120-014-0413-8) contains supplementary material, which is available to authorized users. Springer Japan 2014-08-12 2015 /pmc/articles/PMC4511074/ /pubmed/25112781 http://dx.doi.org/10.1007/s10120-014-0413-8 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Sasako, Mitsuru
Terashima, Masanori
Ichikawa, Wataru
Ochiai, Atsushi
Kitada, Koji
Kurahashi, Issei
Sakuramoto, Shinichi
Katai, Hitoshi
Sano, Takeshi
Imamura, Hiroshi
Impact of the expression of thymidylate synthase and dihydropyrimidine dehydrogenase genes on survival in stage II/III gastric cancer
title Impact of the expression of thymidylate synthase and dihydropyrimidine dehydrogenase genes on survival in stage II/III gastric cancer
title_full Impact of the expression of thymidylate synthase and dihydropyrimidine dehydrogenase genes on survival in stage II/III gastric cancer
title_fullStr Impact of the expression of thymidylate synthase and dihydropyrimidine dehydrogenase genes on survival in stage II/III gastric cancer
title_full_unstemmed Impact of the expression of thymidylate synthase and dihydropyrimidine dehydrogenase genes on survival in stage II/III gastric cancer
title_short Impact of the expression of thymidylate synthase and dihydropyrimidine dehydrogenase genes on survival in stage II/III gastric cancer
title_sort impact of the expression of thymidylate synthase and dihydropyrimidine dehydrogenase genes on survival in stage ii/iii gastric cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511074/
https://www.ncbi.nlm.nih.gov/pubmed/25112781
http://dx.doi.org/10.1007/s10120-014-0413-8
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