<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(1)</volume><submitter>Chang WH</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Despite much progress in cancer research, its incidence and mortality continue to rise. A robust biomarker that would predict tumor behavior is highly desirable and could improve patient treatment and prognosis.&lt;h4>Methods&lt;/h4>In a retrospective bioinformatics analysis involving patients with liver cancer (n?=?839), we developed a prognostic signature consisting of 45 genes associated with tumor-infiltrating lymphocytes and cellular responses to hypoxia. From this gene set, we were able to identify a second prognostic signature comprised of 8 genes. Its performance was further validated in five other cancers: head and neck (n?=?520), renal papillary cell (n?=?290), lung (n?=?515), pancreas (n?=?178) and endometrial (n?=?370).&lt;h4>Results&lt;/h4>The 45-gene signature predicted overall survival in three liver cancer cohorts: hazard ratio (HR)?=?1.82, P?=?0.006; HR?=?1.84, P?=?0.008 and HR?=?2.67, P?=?0.003. Additionally, the reduced 8-gene signature was sufficient and effective in predicting survival in liver and five other cancers: liver (HR?=?2.36, P?=?0.0003; HR?=?2.43, P?=?0.0002 and HR?=?3.45, P?=?0.0007), head and neck (HR?=?1.64, P?=?0.004), renal papillary cell (HR?=?2.31, P?=?0.04), lung (HR?=?1.45, P?=?0.03), pancreas (HR?=?1.96, P?=?0.006) and endometrial (HR?=?2.33, P?=?0.003). Receiver operating characteristic analyses demonstrated both signatures superior performance over current tumor staging parameters. Multivariate Cox regression analyses revealed that both 45-gene and 8-gene signatures were independent of other clinicopathological features in these cancers. Combining the gene signatures with somatic mutation profiles increased their prognostic ability.&lt;h4>Conclusions&lt;/h4>This study, to our knowledge, is the first to identify a gene signature uniting both tumor hypoxia and lymphocytic infiltration as a prognostic determinant in six cancer types (n?=?2712). The 8-gene signature can be used for patient risk stratification by incorporating hypoxia information to aid clinical decision making.</pubmed_abstract><journal>Journal of translational medicine</journal><pagination>14</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6327401</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A novel signature derived from immunoregulatory and hypoxia genes predicts prognosis in liver and five other cancers.</pubmed_title><pmcid>PMC6327401</pmcid><pubmed_authors>Lai AG</pubmed_authors><pubmed_authors>Chang WH</pubmed_authors><pubmed_authors>Forde D</pubmed_authors></additional><is_claimable>false</is_claimable><name>A novel signature derived from immunoregulatory and hypoxia genes predicts prognosis in liver and five other cancers.</name><description>&lt;h4>Background&lt;/h4>Despite much progress in cancer research, its incidence and mortality continue to rise. A robust biomarker that would predict tumor behavior is highly desirable and could improve patient treatment and prognosis.&lt;h4>Methods&lt;/h4>In a retrospective bioinformatics analysis involving patients with liver cancer (n?=?839), we developed a prognostic signature consisting of 45 genes associated with tumor-infiltrating lymphocytes and cellular responses to hypoxia. From this gene set, we were able to identify a second prognostic signature comprised of 8 genes. Its performance was further validated in five other cancers: head and neck (n?=?520), renal papillary cell (n?=?290), lung (n?=?515), pancreas (n?=?178) and endometrial (n?=?370).&lt;h4>Results&lt;/h4>The 45-gene signature predicted overall survival in three liver cancer cohorts: hazard ratio (HR)?=?1.82, P?=?0.006; HR?=?1.84, P?=?0.008 and HR?=?2.67, P?=?0.003. Additionally, the reduced 8-gene signature was sufficient and effective in predicting survival in liver and five other cancers: liver (HR?=?2.36, P?=?0.0003; HR?=?2.43, P?=?0.0002 and HR?=?3.45, P?=?0.0007), head and neck (HR?=?1.64, P?=?0.004), renal papillary cell (HR?=?2.31, P?=?0.04), lung (HR?=?1.45, P?=?0.03), pancreas (HR?=?1.96, P?=?0.006) and endometrial (HR?=?2.33, P?=?0.003). Receiver operating characteristic analyses demonstrated both signatures superior performance over current tumor staging parameters. Multivariate Cox regression analyses revealed that both 45-gene and 8-gene signatures were independent of other clinicopathological features in these cancers. Combining the gene signatures with somatic mutation profiles increased their prognostic ability.&lt;h4>Conclusions&lt;/h4>This study, to our knowledge, is the first to identify a gene signature uniting both tumor hypoxia and lymphocytic infiltration as a prognostic determinant in six cancer types (n?=?2712). The 8-gene signature can be used for patient risk stratification by incorporating hypoxia information to aid clinical decision making.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2021-02-21T03:53:21Z</modification><creation>2019-03-26T22:37:06Z</creation></dates><accession>S-EPMC6327401</accession><cross_references><pubmed>30626396</pubmed><doi>10.1186/s12967-019-1775-9</doi></cross_references></HashMap>