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Changes of Gene Expression of Thymidine Phosphorylase, Thymidylate Synthase, Dihydropyrimidine Dehydrogenase after the Administration of 5'-Deoxy-5-Fluorouridine, Paclitaxel and its Combination in Human Gastric Cancer Xenografts

Although a variety of combination chemotherapies has been tested in gastric carcinoma, the most effective chemotherapeutic regimen and the precise mechanisms underlying anticancer agent combination have not yet been sufficiently elucidated. Experimental chemotherapy was performed using human gastric...

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Published in:Anticancer research 2008-05, Vol.28 (3A), p.1593-1602
Main Authors: SAKURAI, Yoichi, YOSHIDA, Ikuo, KAMOSHIDA, Shingo, INABA, Kazuki, ISOGAKI, Jun, KOMORI, Yoshiyuki, UYAMA, Ichiro, TSUTSUMI, Yutaka
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container_title Anticancer research
container_volume 28
creator SAKURAI, Yoichi
YOSHIDA, Ikuo
KAMOSHIDA, Shingo
INABA, Kazuki
ISOGAKI, Jun
KOMORI, Yoshiyuki
UYAMA, Ichiro
TSUTSUMI, Yutaka
description Although a variety of combination chemotherapies has been tested in gastric carcinoma, the most effective chemotherapeutic regimen and the precise mechanisms underlying anticancer agent combination have not yet been sufficiently elucidated. Experimental chemotherapy was performed using human gastric carcinoma xenografts, MKN-45 and TMK-1, to examine the anticancer effects and gene expressions of the enzymes involved in 5-fluorouracil metabolism, thymidine phosphorylase (dThdPase), thymidylate synthase (TS) and dihydropyrimidine dehydrogenase (DPD). Nude mice were treated with 5'-deoxy-5-fluorouridine (5'-dFUrd), or paclitaxel alone or in combination. The in vivo antitumor effects on gene expressions of the enzymes were examined using the quantitative real-time RT-PCR method. The combined use of 5'-dFUrd and paclitaxel showed additive to synergistic antitumor effects on both gastric cancer xenografts. There were significant differences of the gene expressions of dThdPase, TS, and DPD between the xenografts. The expression of dThdPase mRNA was consistently up-regulated by the administration of paclitaxel, while no constant direction of TS mRNA and DPD mRNA change was found in the xenografts. A synergistic antitumor effect of the combined administration of 5'-dFUrd and paclitaxel was found in gastric cancer xenografts and up-regulation of dThdPase mRNA may be an important underlying mechanism especially in tumors with high gene expression of this enzyme.
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subjects Animals
Antineoplastic Combined Chemotherapy Protocols - pharmacokinetics
Antineoplastic Combined Chemotherapy Protocols - pharmacology
Biological and medical sciences
Body Weight
Dihydrouracil Dehydrogenase (NADP) - biosynthesis
Dihydrouracil Dehydrogenase (NADP) - genetics
Dihydrouracil Dehydrogenase (NADP) - metabolism
Floxuridine - administration & dosage
Floxuridine - pharmacokinetics
Floxuridine - pharmacology
Gastroenterology. Liver. Pancreas. Abdomen
Gene Expression - drug effects
Humans
Male
Medical sciences
Mice
Mice, Inbred BALB C
Mice, Nude
Paclitaxel - administration & dosage
Paclitaxel - pharmacokinetics
Paclitaxel - pharmacology
RNA, Messenger - biosynthesis
RNA, Messenger - genetics
Stomach Neoplasms - drug therapy
Stomach Neoplasms - enzymology
Stomach Neoplasms - genetics
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Thymidine Phosphorylase - biosynthesis
Thymidine Phosphorylase - genetics
Thymidine Phosphorylase - metabolism
Thymidylate Synthase - biosynthesis
Thymidylate Synthase - genetics
Thymidylate Synthase - metabolism
Tumors
Xenograft Model Antitumor Assays
title Changes of Gene Expression of Thymidine Phosphorylase, Thymidylate Synthase, Dihydropyrimidine Dehydrogenase after the Administration of 5'-Deoxy-5-Fluorouridine, Paclitaxel and its Combination in Human Gastric Cancer Xenografts
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