<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE307nnn/GSE307202/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Homo sapiens</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE307202</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>An androgen receptor pre-mRNA stem loop structure determines splicing fate of AR-V7 in prostate cancer</name><description>In castration-resistant prostate cancer (CRPC), detection of androgen receptor (AR) splice isoform AR-V7 correlates strongly with resistance to AR pathway inhibitors (ARPI) and poor patient outcomes. AR-V7 incorporates transcript-terminating cryptic exon 3 (CE3), which excludes the ligand binding domain from the AR protein, thereby enabling AR-driven transcriptional regulation independent of androgens. While several CE3 splicing regulatory proteins have been described, the impact of pre-mRNA structures in this region is unknown. We performed SHAPE-MaP to develop the first experimentally informed secondary structure model of the CE3 3' splice site. This model predicted a previously undescribed RNA stem loop structure, which we hypothesized could inhibit AR-V7 biogenesis. Using an AR-V7 minigene assay, we observed decreased AR-V7 abundance in response to stabilization of this structure, leading us to term it the cryptic exon 3-splicing inhibitory stem loop (CE3-SISL). ∆SHAPE analysis supported a protein interaction at this site that is lost in androgen independence. Using quantitative proteomics, we nominated candidate interactors, such as neuro-oncological ventral antigen 1 (NOVA1), that may help explain the repressive function of CE3-SISL. Together, these data support the importance of this RNA structure in AR-V7 biogenesis and suggest a potential target for AR-V7-depleting agents. As a proof of concept, we developed several CE3-SISL-targeting antisense oligonucleotides (ASOs), which showed almost complete inhibition of AR-V7 biogenesis in both the minigene assay and in endogenous AR-V7-expressing cells with or without the ARPI enzalutamide. CE3-SISL is therefore functional in AR-V7 biogenesis and can serve as a structural target in therapeutic development for AR-V7-driven CRPC.</description><dates><publication>2026/08/29</publication></dates><accession>GSE307202</accession><cross_references><GSM>GSM9218809</GSM><GSM>GSM9218804</GSM><GSM>GSM9218815</GSM><GSM>GSM9218814</GSM><GSM>GSM9218813</GSM><GSM>GSM9218812</GSM><GSM>GSM9218823</GSM><GSM>GSM9218808</GSM><GSM>GSM9218819</GSM><GSM>GSM9218807</GSM><GSM>GSM9218818</GSM><GSM>GSM9218817</GSM><GSM>GSM9218806</GSM><GSM>GSM9218805</GSM><GSM>GSM9218816</GSM><GSM>GSM9218811</GSM><GSM>GSM9218822</GSM><GSM>GSM9218821</GSM><GSM>GSM9218810</GSM><GSM>GSM9218820</GSM><GPL>15520</GPL><GSE>307202</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>