<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Farrell JJ</submitter><funding>NCATS NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>1485-1493</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5119656</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>45(10)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>There is a need for validated predictive markers of gemcitabine response to guide precision medicine treatment in pancreatic cancer. We previously validated human equilibrative nucleoside transporter 1 as a predictive marker of gemcitabine treatment response using Radiation Therapy Oncology Group 9704. Controversy exists about the predictive value of gemcitabine metabolism pathway biomarkers: deoxycytidine kinase (DCK), ribonucleotide reductase 1 (RRM1), RRM2, and p53R2.&lt;h4>Methods&lt;/h4>Radiation Therapy Oncology Group 9704 prospectively randomized 538 patients after pancreatic resection to receive either 5-fluorouracil or gemcitabine. Tumor DCK, RRM1, RRM2, and p53R protein expressions were analyzed using a tissue microarray and immunohistochemistry and correlated with t</pubmed_abstract><journal>Pancreas</journal><pubmed_title>Precision Medicine and Pancreatic Cancer: A Gemcitabine Pathway Approach.</pubmed_title><pmcid>PMC5119656</pmcid><funding_grant_id>U24 CA114734</funding_grant_id><funding_grant_id>P30 CA060553</funding_grant_id><funding_grant_id>U10 CA180868</funding_grant_id><funding_grant_id>U10 CA180822</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><pubmed_authors>Zheng Z</pubmed_authors><pubmed_authors>Guha C</pubmed_authors><pubmed_authors>Schaefer P</pubmed_authors><pubmed_authors>Elsaleh H</pubmed_authors><pubmed_authors>Macdonald JS</pubmed_authors><pubmed_authors>Regine WF</pubmed_authors><pubmed_authors>Benson AB</pubmed_authors><pubmed_authors>Yen Y</pubmed_authors><pubmed_authors>Moughan J</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Bepler G</pubmed_authors><pubmed_authors>Wong JL</pubmed_authors><pubmed_authors>Farrell JJ</pubmed_authors><pubmed_authors>Lai R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Precision Medicine and Pancreatic Cancer: A Gemcitabine Pathway Approach.</name><description>&lt;h4>Objectives&lt;/h4>There is a need for validated predictive markers of gemcitabine response to guide precision medicine treatment in pancreatic cancer. We previously validated human equilibrative nucleoside transporter 1 as a predictive marker of gemcitabine treatment response using Radiation Therapy Oncology Group 9704. Controversy exists about the predictive value of gemcitabine metabolism pathway biomarkers: deoxycytidine kinase (DCK), ribonucleotide reductase 1 (RRM1), RRM2, and p53R2.&lt;h4>Methods&lt;/h4>Radiation Therapy Oncology Group 9704 prospectively randomized 538 patients after pancreatic resection to receive either 5-fluorouracil or gemcitabine. Tumor DCK, RRM1, RRM2, and p53R protein expressions were analyzed using a tissue microarray and immunohistochemistry and correlated with t</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Nov</publication><modification>2025-04-27T01:21:50.252Z</modification><creation>2019-03-27T02:29:35Z</creation></dates><accession>S-EPMC5119656</accession><cross_references><pubmed>27748721</pubmed><doi>10.1097/MPA.0000000000000710</doi><doi>10.1097/mpa.0000000000000710</doi></cross_references></HashMap>