<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Harris CS</submitter><funding>American Cancer Society</funding><funding>International Society of Nurses in Genetics</funding><funding>National Institute of Nursing Research</funding><funding>NINR NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><pagination>51-64</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9900252</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(1)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>While the gastrointestinal symptom cluster (GISC) is common in patients receiving chemotherapy, limited information is available on its underlying mechanism(s). Emerging evidence suggests a role for inflammatory processes through the actions of the nuclear factor kappa B (NF-κB) signaling pathway. This study evaluated for associations between a GISC and levels of DNA methylation for genes within this pathway.&lt;h4>Methods&lt;/h4>Prior to their second or third cycle of chemotherapy, 1071 outpatients reported symptom occurrence using the Memorial Symptom Assessment Scale. A GISC was identified using exploratory factor analysis. Differential methylation analyses were performed in two independent samples using EPIC (&lt;i>n&lt;/i> = 925) and 450K (&lt;i>n&lt;/i> = 146) microarrays. Trans exp</pubmed_abstract><journal>Biological research for nursing</journal><pubmed_title>Gastrointestinal Symptom Cluster is Associated With Epigenetic Regulation of Lymphotoxin Beta in Oncology Patients Receiving Chemotherapy.</pubmed_title><pmcid>PMC9900252</pmcid><funding_grant_id>T32 NR009759</funding_grant_id><funding_grant_id>Research Grant</funding_grant_id><funding_grant_id>R37 CA233774</funding_grant_id><funding_grant_id>P30 CA082103</funding_grant_id><funding_grant_id>Doctoral Degree Scholarship</funding_grant_id><funding_grant_id>NR016920</funding_grant_id><funding_grant_id>CA233774</funding_grant_id><funding_grant_id>T32 NR016920</funding_grant_id><funding_grant_id>CA134900</funding_grant_id><funding_grant_id>R01 CA134900</funding_grant_id><pubmed_authors>Harris CS</pubmed_authors><pubmed_authors>Conley YP</pubmed_authors><pubmed_authors>Olshen AB</pubmed_authors><pubmed_authors>Levine JD</pubmed_authors><pubmed_authors>Hammer MJ</pubmed_authors><pubmed_authors>Miaskowski CA</pubmed_authors><pubmed_authors>Kober KM</pubmed_authors><pubmed_authors>Dhruva AA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gastrointestinal Symptom Cluster is Associated With Epigenetic Regulation of Lymphotoxin Beta in Oncology Patients Receiving Chemotherapy.</name><description>&lt;h4>Objectives&lt;/h4>While the gastrointestinal symptom cluster (GISC) is common in patients receiving chemotherapy, limited information is available on its underlying mechanism(s). Emerging evidence suggests a role for inflammatory processes through the actions of the nuclear factor kappa B (NF-κB) signaling pathway. This study evaluated for associations between a GISC and levels of DNA methylation for genes within this pathway.&lt;h4>Methods&lt;/h4>Prior to their second or third cycle of chemotherapy, 1071 outpatients reported symptom occurrence using the Memorial Symptom Assessment Scale. A GISC was identified using exploratory factor analysis. Differential methylation analyses were performed in two independent samples using EPIC (&lt;i>n&lt;/i> = 925) and 450K (&lt;i>n&lt;/i> = 146) microarrays. Trans exp</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-03-16T09:35:24.892Z</modification><creation>2025-04-05T15:54:01.006Z</creation></dates><accession>S-EPMC9900252</accession><cross_references><pubmed>35929442</pubmed><doi>10.1177/10998004221115863</doi></cross_references></HashMap>