HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Human equilibrative nucleoside transporter 1 expression is a strong independent prognostic factor in UICC T3-T4 pancreatic cancer patients treated with preoperative gemcitabine-based chemoradiotherapy.

AbstractBACKGROUND/PURPOSE:
We aimed to determine the relationship between the intratumoral expression of human equilibrative nucleoside transporter (hENT1), the main gemcitabine transporter into cells, and the outcome of gemcitabine-based chemoradiotherapy (Gem-CRT) in patients with International Union Against Cancer (UICC) T3-T4 pancreatic adenocarcinoma.
METHODS:
The expressions of hENT1, thymidylate synthase (TS), and dihydropyrimidine dehydrogenase were immunohistochemically analyzed using the resected specimens from 55 patients (T3, 38 and T4, 17) who had received curative-intent resection after Gem-CRT.
RESULTS:
The status of hENT1 expression (positive in 39 and negative in 16) was significantly associated with "clinical efficacy" (defined as more than 50% reduction of the serum carbohydrate antigen [CA] 19-9 level with stable disease [SD] or partial response [PR] according to the Response Evaluation Criteria in Solid Tumors [RECIST]) for Gem-CRT. The 1- and 3-year overall survival (OS) rates were significantly higher in the positive hENT1 expression group (82.9, 39.5%) than in the negative expression group (42.9, 14.3%) (p = 0.0037). According to combination analysis of hENT1 and TS expressions, the 1- and 3-year OS rates were significantly higher in the positive-low combination (89.1, 51.0%) group than in the negative-high group (66.7, 0%) (p = 0.023). Multivariate analysis revealed that positive hENT1 expression and R0 resection were significant prognostic factors for OS.
CONCLUSIONS:
The hENT1 expression in pancreatic adenocarcinoma strongly influences the outcome of preoperative Gem-CRT treatment. This biomarker could become a useful predictor of therapeutic effect for gemcitabine-based therapy in pancreatic cancer patients.
AuthorsYasuhiro Murata, Takashi Hamada, Masashi Kishiwada, Ichiro Ohsawa, Shugo Mizuno, Masanobu Usui, Hiroyuki Sakurai, Masami Tabata, Noriko Ii, Hiroyuki Inoue, Taizo Shiraishi, Shuji Isaji
JournalJournal of hepato-biliary-pancreatic sciences (J Hepatobiliary Pancreat Sci) Vol. 19 Issue 4 Pg. 413-25 (Jul 2012) ISSN: 1868-6982 [Electronic] Japan
PMID21898089 (Publication Type: Journal Article)
Chemical References
  • Biomarkers
  • CA-19-9 Antigen
  • Equilibrative Nucleoside Transporter 1
  • SLC29A1 protein, human
  • Dihydrouracil Dehydrogenase (NADP)
  • Thymidylate Synthase
Topics
  • Adenocarcinoma (metabolism, mortality, pathology, surgery, therapy)
  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers (analysis)
  • CA-19-9 Antigen (blood)
  • Chemoradiotherapy, Adjuvant
  • Dihydrouracil Dehydrogenase (NADP) (metabolism)
  • Equilibrative Nucleoside Transporter 1 (metabolism)
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Neoadjuvant Therapy
  • Neoplasm Staging
  • Nutrition Assessment
  • Pancreatic Neoplasms (metabolism, mortality, pathology, surgery, therapy)
  • Prognosis
  • Survival Analysis
  • Thymidylate Synthase (metabolism)
  • Treatment Outcome

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: