<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hosseini TM</submitter><funding>University of California San Diego Altman Clinical and Translational Research Institute</funding><funding>NCI NIH HHS</funding><pagination>1072</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11987906</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(7)</volume><pubmed_abstract>&lt;b>Background/Objectives&lt;/b>: HPV+ head and neck squamous cell carcinoma has been shown to have a unique genomic background, requiring researchers to study it as its own distinct type of cancer. HPV+ tumors have been shown to exhibit fewer genetic mutations in cancer drivers as opposed to their HPV- counterparts. In this paper, we explored how targeting post-transcriptional changes, specifically alternative splicing events, could serve as a potential mechanism to treat HPV+ cancer. &lt;b>Methods&lt;/b>: Using indisulam, a drug that targets alternative splicing through the degradation of RBM39, we treated various HPV+ and HPV- cell lines and assessed tumor cell viability. We also tested indisulam in vivo to evaluate its effect on tumor volume. Additionally, we analyzed gene expression differences</pubmed_abstract><journal>Cancers</journal><pubmed_title>Indisulam Shows an Anti-Cancer Effect on HPV+ and HPV- Head and Neck Cancer.</pubmed_title><pmcid>PMC11987906</pmcid><funding_grant_id>1KL2TR001444</funding_grant_id><funding_grant_id>1K08CA276999-01A1</funding_grant_id><pubmed_authors>Jang SS</pubmed_authors><pubmed_authors>Guo T</pubmed_authors><pubmed_authors>Hosseini TM</pubmed_authors><pubmed_authors>Bendik J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Indisulam Shows an Anti-Cancer Effect on HPV+ and HPV- Head and Neck Cancer.</name><description>&lt;b>Background/Objectives&lt;/b>: HPV+ head and neck squamous cell carcinoma has been shown to have a unique genomic background, requiring researchers to study it as its own distinct type of cancer. HPV+ tumors have been shown to exhibit fewer genetic mutations in cancer drivers as opposed to their HPV- counterparts. In this paper, we explored how targeting post-transcriptional changes, specifically alternative splicing events, could serve as a potential mechanism to treat HPV+ cancer. &lt;b>Methods&lt;/b>: Using indisulam, a drug that targets alternative splicing through the degradation of RBM39, we treated various HPV+ and HPV- cell lines and assessed tumor cell viability. We also tested indisulam in vivo to evaluate its effect on tumor volume. Additionally, we analyzed gene expression differences</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-07-03T03:06:05.869Z</modification><creation>2025-07-03T03:06:05.869Z</creation></dates><accession>S-EPMC11987906</accession><cross_references><pubmed>40227602</pubmed><doi>10.3390/cancers17071072</doi></cross_references></HashMap>