<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nfonsam V</submitter><funding>NCI NIH HHS</funding><pagination>1005</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5321608</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>1(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Overall declines in incidence of rectal cancer (RC) in patients older than 50 years have been mostly attributed to improvement in treatment modalities and introduction of age-based screening. Recent studies, however, have shown a rise in the incidence of RC in patients younger than 50 years. The etiology of early-onset (EO) RC is not well understood. The aim of this study is to elucidate the molecular features of (EO) RC and show its uniqueness compared to late-onset (LO) disease.&lt;h4>Methods&lt;/h4>Two cohorts of patients with sporadic RC were identified. Tumors and matching non-involved tissues from six (EO) RC patients (&lt; 50 years) and six (LO) RC patients (>65 years) were obtained from Pathology archives. Deparaffinized tissues were macro-dissected from FFPE sections, RN</pubmed_abstract><journal>Gastrointestinal cancer : research &amp; therapy</journal><pubmed_title>Gene Expression Analysis of Sporadic Early-Onset Rectal Adenocarcinoma.</pubmed_title><pmcid>PMC5321608</pmcid><funding_grant_id>P30 CA023074</funding_grant_id><pubmed_authors>Nfonsam V</pubmed_authors><pubmed_authors>Jandova J</pubmed_authors><pubmed_authors>Koblinski J</pubmed_authors><pubmed_authors>Xu W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gene Expression Analysis of Sporadic Early-Onset Rectal Adenocarcinoma.</name><description>&lt;h4>Background&lt;/h4>Overall declines in incidence of rectal cancer (RC) in patients older than 50 years have been mostly attributed to improvement in treatment modalities and introduction of age-based screening. Recent studies, however, have shown a rise in the incidence of RC in patients younger than 50 years. The etiology of early-onset (EO) RC is not well understood. The aim of this study is to elucidate the molecular features of (EO) RC and show its uniqueness compared to late-onset (LO) disease.&lt;h4>Methods&lt;/h4>Two cohorts of patients with sporadic RC were identified. Tumors and matching non-involved tissues from six (EO) RC patients (&lt; 50 years) and six (LO) RC patients (>65 years) were obtained from Pathology archives. Deparaffinized tissues were macro-dissected from FFPE sections, RN</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2025-04-04T02:09:15.574Z</modification><creation>2019-03-27T02:37:07Z</creation></dates><accession>S-EPMC5321608</accession><cross_references><pubmed>28239680</pubmed></cross_references></HashMap>