<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chaubal R</submitter><funding>Department of Atomic Energy, Government of India</funding><funding>Mizuho Bank Limited</funding><funding>Akhil Gupta</funding><funding>Sunil Gupta</funding><funding>Department of Atomic Energy, Government of India (DAE)</funding><funding>Department of Biotechnology, Ministry of Science and Technology, India (DBT)</funding><funding>Department of Biotechnology, Ministry of Science and Technology, India</funding><funding>Womens Cancer Initiative</funding><pagination>572-584</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11148542</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(6)</volume><pubmed_abstract>Surgery exposes tumor tissue to severe hypoxia and mechanical stress leading to rapid gene expression changes in the tumor and its microenvironment, which remain poorly characterized. We biopsied tumor and adjacent normal tissues from patients with breast (n = 81) and head/neck squamous cancers (HNSC; n = 10) at the beginning (A), during (B), and end of surgery (C). Tumor/normal RNA from 46/81 patients with breast cancer was subjected to mRNA-Seq using Illumina short-read technology, and from nine patients with HNSC to whole-transcriptome microarray with Illumina BeadArray. Pathways and genes involved in 7 of 10 known cancer hallmarks, namely, tumor-promoting inflammation (TNF-A, NFK-B, IL18 pathways), activation of invasion and migration (various extracellular matrix-related pathways, cel</pubmed_abstract><journal>Molecular cancer research : MCR</journal><pubmed_title>Surgical Tumor Resection Deregulates Hallmarks of Cancer in Resected Tissue and the Surrounding Microenvironment.</pubmed_title><pmcid>PMC11148542</pmcid><funding_grant_id>Research Grant</funding_grant_id><funding_grant_id>BT/MED/30/VNCI-Hr-BRCA/2015</funding_grant_id><funding_grant_id>Personal Research Grant for Laboratory Infrastructure from Mr. Akhil Gupta</funding_grant_id><funding_grant_id>DAE CTC-TMC</funding_grant_id><funding_grant_id>Personal Research Grant from Mr. Sunil Gupta Formerly at Tata Motors</funding_grant_id><funding_grant_id>Corporate Social Responsibility Research Grant for Institutional Infrastructure</funding_grant_id><pubmed_authors>Dutt A</pubmed_authors><pubmed_authors>Talker E</pubmed_authors><pubmed_authors>Parmar V</pubmed_authors><pubmed_authors>Gupta S</pubmed_authors><pubmed_authors>Kadam R</pubmed_authors><pubmed_authors>Shetty O</pubmed_authors><pubmed_authors>Pantvaidya G</pubmed_authors><pubmed_authors>Hawaldar R</pubmed_authors><pubmed_authors>Kalkar P</pubmed_authors><pubmed_authors>Krishnan NM</pubmed_authors><pubmed_authors>Nair N</pubmed_authors><pubmed_authors>Panda B</pubmed_authors><pubmed_authors>Vanmali V</pubmed_authors><pubmed_authors>Desai S</pubmed_authors><pubmed_authors>Gera P</pubmed_authors><pubmed_authors>Chitra J</pubmed_authors><pubmed_authors>Gurav M</pubmed_authors><pubmed_authors>Bhatia D</pubmed_authors><pubmed_authors>Gardi N</pubmed_authors><pubmed_authors>Joshi S</pubmed_authors><pubmed_authors>Chaubal R</pubmed_authors><pubmed_authors>Badwe R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Surgical Tumor Resection Deregulates Hallmarks of Cancer in Resected Tissue and the Surrounding Microenvironment.</name><description>Surgery exposes tumor tissue to severe hypoxia and mechanical stress leading to rapid gene expression changes in the tumor and its microenvironment, which remain poorly characterized. We biopsied tumor and adjacent normal tissues from patients with breast (n = 81) and head/neck squamous cancers (HNSC; n = 10) at the beginning (A), during (B), and end of surgery (C). Tumor/normal RNA from 46/81 patients with breast cancer was subjected to mRNA-Seq using Illumina short-read technology, and from nine patients with HNSC to whole-transcriptome microarray with Illumina BeadArray. Pathways and genes involved in 7 of 10 known cancer hallmarks, namely, tumor-promoting inflammation (TNF-A, NFK-B, IL18 pathways), activation of invasion and migration (various extracellular matrix-related pathways, cel</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2026-06-02T10:35:00.753Z</modification><creation>2026-05-27T03:07:44.134Z</creation></dates><accession>S-EPMC11148542</accession><cross_references><pubmed>38394149</pubmed><doi>10.1158/1541-7786.MCR-23-0265</doi></cross_references></HashMap>