<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu Z</submitter><funding>NCATS NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>394-400</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4679504</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>139(3)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Suboptimal cytoreductive surgery in advanced epithelial ovarian cancer (EOC) is associated with poor survival but it is unknown if poor outcome is due to the intrinsic biology of unresectable tumors or insufficient surgical effort resulting in residual tumor-sustaining clones. Our objective was to identify the potential molecular pathway(s) and cell type(s) that may be responsible for suboptimal surgical resection.&lt;h4>Methods&lt;/h4>By comparing gene expression in optimally and suboptimally cytoreduced patients, we identified a gene network associated with suboptimal cytoreduction and explored the biological processes and cell types associated with this gene network.&lt;h4>Results&lt;/h4>We show that primary tumors from suboptimally cytoreduced patients express molecular signature</pubmed_abstract><journal>Gynecologic oncology</journal><pubmed_title>Suboptimal cytoreduction in ovarian carcinoma is associated with molecular pathways characteristic of increased stromal activation.</pubmed_title><pmcid>PMC4679504</pmcid><funding_grant_id>R21 CA194626</funding_grant_id><funding_grant_id>UL1 TR000124</funding_grant_id><pubmed_authors>Agadjanian H</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Karlan BY</pubmed_authors><pubmed_authors>Jia D</pubmed_authors><pubmed_authors>Aspuria PJ</pubmed_authors><pubmed_authors>Orsulic S</pubmed_authors><pubmed_authors>Beach JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Suboptimal cytoreduction in ovarian carcinoma is associated with molecular pathways characteristic of increased stromal activation.</name><description>&lt;h4>Objective&lt;/h4>Suboptimal cytoreductive surgery in advanced epithelial ovarian cancer (EOC) is associated with poor survival but it is unknown if poor outcome is due to the intrinsic biology of unresectable tumors or insufficient surgical effort resulting in residual tumor-sustaining clones. Our objective was to identify the potential molecular pathway(s) and cell type(s) that may be responsible for suboptimal surgical resection.&lt;h4>Methods&lt;/h4>By comparing gene expression in optimally and suboptimally cytoreduced patients, we identified a gene network associated with suboptimal cytoreduction and explored the biological processes and cell types associated with this gene network.&lt;h4>Results&lt;/h4>We show that primary tumors from suboptimally cytoreduced patients express molecular signature</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Dec</publication><modification>2025-05-31T22:22:28.671Z</modification><creation>2020-10-29T11:02:01Z</creation></dates><accession>S-EPMC4679504</accession><cross_references><pubmed>26348314</pubmed><doi>10.1016/j.ygyno.2015.08.026</doi></cross_references></HashMap>