<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Qu S</submitter><funding>Intramural NIH HHS</funding><funding>National Cancer Institute</funding><pagination>141-153</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8692365</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(1)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>A new molecular subtype classification was recently proposed for SCLC. It is necessary to validate it in primary SCLC tumors by immunohistochemical (IHC) staining and define its clinical relevance.&lt;h4>Methods&lt;/h4>We used IHC to assess four subtype markers (ASCL1, NEUROD1, POU2F3, and YAP1) in 194 cores from 146 primary SCLC tumors. The profiles of tumor-associated CD3&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> T-cells, MYC paralogs, SLFN11, and SYP were compared among different subtypes. Validation was performed using publicly available RNA sequencing data of SCLC.&lt;h4>Results&lt;/h4>ASCL1, NEUROD1, POU2F3, and YAP1 were the dominant molecular subtypes in 78.2%, 5.6%, 7%, and 2.8% of the tumors, respectively; 6.3% of the tumors were negative for all four subtype markers. Notably, thr</pubmed_abstract><journal>Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer</journal><pubmed_title>Molecular Subtypes of Primary SCLC Tumors and Their Associations With Neuroendocrine and Therapeutic Markers.</pubmed_title><pmcid>PMC8692365</pmcid><funding_grant_id>BC006161</funding_grant_id><funding_grant_id>ZIA BC011787</funding_grant_id><funding_grant_id>Z01 BC006161</funding_grant_id><funding_grant_id>ZIA BC011839</funding_grant_id><pubmed_authors>Schrump DS</pubmed_authors><pubmed_authors>Qu S</pubmed_authors><pubmed_authors>Pommier Y</pubmed_authors><pubmed_authors>Thomas A</pubmed_authors><pubmed_authors>Chen H</pubmed_authors><pubmed_authors>Miettinen MM</pubmed_authors><pubmed_authors>Fetsch P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular Subtypes of Primary SCLC Tumors and Their Associations With Neuroendocrine and Therapeutic Markers.</name><description>&lt;h4>Introduction&lt;/h4>A new molecular subtype classification was recently proposed for SCLC. It is necessary to validate it in primary SCLC tumors by immunohistochemical (IHC) staining and define its clinical relevance.&lt;h4>Methods&lt;/h4>We used IHC to assess four subtype markers (ASCL1, NEUROD1, POU2F3, and YAP1) in 194 cores from 146 primary SCLC tumors. The profiles of tumor-associated CD3&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> T-cells, MYC paralogs, SLFN11, and SYP were compared among different subtypes. Validation was performed using publicly available RNA sequencing data of SCLC.&lt;h4>Results&lt;/h4>ASCL1, NEUROD1, POU2F3, and YAP1 were the dominant molecular subtypes in 78.2%, 5.6%, 7%, and 2.8% of the tumors, respectively; 6.3% of the tumors were negative for all four subtype markers. Notably, thr</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-04-26T00:23:28.229Z</modification><creation>2024-11-20T04:35:52.467Z</creation></dates><accession>S-EPMC8692365</accession><cross_references><pubmed>34534680</pubmed><doi>10.1016/j.jtho.2021.08.763</doi></cross_references></HashMap>