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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 |
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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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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.</description><identifier>ISSN: 0250-7005</identifier><identifier>EISSN: 1791-7530</identifier><identifier>PMID: 18630517</identifier><language>eng</language><publisher>Attiki: International Institute of Anticancer Research</publisher><subject>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</subject><ispartof>Anticancer research, 2008-05, Vol.28 (3A), p.1593-1602</ispartof><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20445196$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18630517$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SAKURAI, Yoichi</creatorcontrib><creatorcontrib>YOSHIDA, Ikuo</creatorcontrib><creatorcontrib>KAMOSHIDA, Shingo</creatorcontrib><creatorcontrib>INABA, Kazuki</creatorcontrib><creatorcontrib>ISOGAKI, Jun</creatorcontrib><creatorcontrib>KOMORI, Yoshiyuki</creatorcontrib><creatorcontrib>UYAMA, Ichiro</creatorcontrib><creatorcontrib>TSUTSUMI, Yutaka</creatorcontrib><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</title><title>Anticancer research</title><addtitle>Anticancer Res</addtitle><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.</description><subject>Animals</subject><subject>Antineoplastic Combined Chemotherapy Protocols - pharmacokinetics</subject><subject>Antineoplastic Combined Chemotherapy Protocols - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Body Weight</subject><subject>Dihydrouracil Dehydrogenase (NADP) - biosynthesis</subject><subject>Dihydrouracil Dehydrogenase (NADP) - genetics</subject><subject>Dihydrouracil Dehydrogenase (NADP) - metabolism</subject><subject>Floxuridine - administration & dosage</subject><subject>Floxuridine - pharmacokinetics</subject><subject>Floxuridine - pharmacology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gene Expression - drug effects</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Paclitaxel - administration & dosage</subject><subject>Paclitaxel - pharmacokinetics</subject><subject>Paclitaxel - pharmacology</subject><subject>RNA, Messenger - biosynthesis</subject><subject>RNA, Messenger - genetics</subject><subject>Stomach Neoplasms - drug therapy</subject><subject>Stomach Neoplasms - enzymology</subject><subject>Stomach Neoplasms - genetics</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Thymidine Phosphorylase - biosynthesis</subject><subject>Thymidine Phosphorylase - genetics</subject><subject>Thymidine Phosphorylase - metabolism</subject><subject>Thymidylate Synthase - biosynthesis</subject><subject>Thymidylate Synthase - genetics</subject><subject>Thymidylate Synthase - metabolism</subject><subject>Tumors</subject><subject>Xenograft Model Antitumor Assays</subject><issn>0250-7005</issn><issn>1791-7530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1DAQhiMEokvhFZAvwKWRHDu2k2OVbbdIlajEHritvPZ4Y5TYwXakzfv2QTDbwJXTaH5_8_8az6tiU4m2KgWj-HWxwYThUmDMrop3Mf7EmPO2oW-Lq6rhFLNKbIrnrpfuBBF5g3bgAN2dpwAxWu_-SPt-Ga22WX_qfZx6H5ZBRrhZH3KTAH1fXOov6tb2iw5-WoJdx7ZwUU7gMoCkSRBQ6gHd6tE6G1OQaY1iX8ot-PNSsvJ-mH3wc7hY3KAnqQab5BkGJJ1GNkXU-fFo3cusdehhHqVDO5n9rEKddCrH_ADnTyFHxvfFGyOHCB_Wel3s7-_23UP5-G33tbt9LCcicCrNUXBeM6MMEY1WXFSU6kbquj2KljS5MY1SulIYuGKk4VJTMMQYhnFNDb0uPr_YTsH_miGmw2ijgmGQDvwcD7ylFSUc_xckGNO6xW0GP67gfBxBH6b8rzIsh7_3y8CnFZBRycGEvLqN_ziC65pVLae_AYlSqoc</recordid><startdate>20080501</startdate><enddate>20080501</enddate><creator>SAKURAI, Yoichi</creator><creator>YOSHIDA, Ikuo</creator><creator>KAMOSHIDA, Shingo</creator><creator>INABA, Kazuki</creator><creator>ISOGAKI, Jun</creator><creator>KOMORI, Yoshiyuki</creator><creator>UYAMA, Ichiro</creator><creator>TSUTSUMI, Yutaka</creator><general>International Institute of Anticancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20080501</creationdate><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</title><author>SAKURAI, Yoichi ; YOSHIDA, Ikuo ; KAMOSHIDA, Shingo ; INABA, Kazuki ; ISOGAKI, Jun ; KOMORI, Yoshiyuki ; UYAMA, Ichiro ; TSUTSUMI, Yutaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p270t-fb76645fcf278dc67133d8ad49b792833df8ccd1c0e6c5286ad3ef2ff50043f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Antineoplastic Combined Chemotherapy Protocols - pharmacokinetics</topic><topic>Antineoplastic Combined Chemotherapy Protocols - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Body Weight</topic><topic>Dihydrouracil Dehydrogenase (NADP) - biosynthesis</topic><topic>Dihydrouracil Dehydrogenase (NADP) - genetics</topic><topic>Dihydrouracil Dehydrogenase (NADP) - metabolism</topic><topic>Floxuridine - administration & dosage</topic><topic>Floxuridine - pharmacokinetics</topic><topic>Floxuridine - pharmacology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Gene Expression - drug effects</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Paclitaxel - administration & dosage</topic><topic>Paclitaxel - pharmacokinetics</topic><topic>Paclitaxel - pharmacology</topic><topic>RNA, Messenger - biosynthesis</topic><topic>RNA, Messenger - genetics</topic><topic>Stomach Neoplasms - drug therapy</topic><topic>Stomach Neoplasms - enzymology</topic><topic>Stomach Neoplasms - genetics</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Thymidine Phosphorylase - biosynthesis</topic><topic>Thymidine Phosphorylase - genetics</topic><topic>Thymidine Phosphorylase - metabolism</topic><topic>Thymidylate Synthase - biosynthesis</topic><topic>Thymidylate Synthase - genetics</topic><topic>Thymidylate Synthase - metabolism</topic><topic>Tumors</topic><topic>Xenograft Model Antitumor Assays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SAKURAI, Yoichi</creatorcontrib><creatorcontrib>YOSHIDA, Ikuo</creatorcontrib><creatorcontrib>KAMOSHIDA, Shingo</creatorcontrib><creatorcontrib>INABA, Kazuki</creatorcontrib><creatorcontrib>ISOGAKI, Jun</creatorcontrib><creatorcontrib>KOMORI, Yoshiyuki</creatorcontrib><creatorcontrib>UYAMA, Ichiro</creatorcontrib><creatorcontrib>TSUTSUMI, Yutaka</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Anticancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SAKURAI, Yoichi</au><au>YOSHIDA, Ikuo</au><au>KAMOSHIDA, Shingo</au><au>INABA, Kazuki</au><au>ISOGAKI, Jun</au><au>KOMORI, Yoshiyuki</au><au>UYAMA, Ichiro</au><au>TSUTSUMI, Yutaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>Anticancer research</jtitle><addtitle>Anticancer Res</addtitle><date>2008-05-01</date><risdate>2008</risdate><volume>28</volume><issue>3A</issue><spage>1593</spage><epage>1602</epage><pages>1593-1602</pages><issn>0250-7005</issn><eissn>1791-7530</eissn><abstract>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.</abstract><cop>Attiki</cop><pub>International Institute of Anticancer Research</pub><pmid>18630517</pmid><tpages>10</tpages></addata></record> |
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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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