<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>45(6)</volume><submitter>Wu Y</submitter><funding>Monash University</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>In prostate cancer, the tumour microenvironment (TME) represents an important regulator of disease progression and response to treatment. In the TME, cancer-associated fibroblasts (CAFs) play a key role in tumour progression, however the mechanisms underpinning fibroblast-cancer cell interactions are incompletely resolved. Here, we address this by applying cell type-specific labelling with amino acid precursors (CTAP) and mass spectrometry (MS)-based (phospho)proteomics to prostate cancer for the first time.&lt;h4>Methods&lt;/h4>Reciprocal interactions between PC3 prostate cancer cells co-cultured with WPMY-1 prostatic fibroblasts were characterised using CTAP-MS. Signalling network changes were determined using Metascape and Enrichr and visualised using Cytoscape. Thymosin β4</pubmed_abstract><journal>Cellular oncology (Dordrecht, Netherlands)</journal><pagination>1311-1328</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9747870</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Proteomic characterisation of prostate cancer intercellular communication reveals cell type-selective signalling and TMSB4X-dependent fibroblast reprogramming.</pubmed_title><pmcid>PMC9747870</pmcid><pubmed_authors>Horvath LG</pubmed_authors><pubmed_authors>Nguyen EV</pubmed_authors><pubmed_authors>Taylor RA</pubmed_authors><pubmed_authors>Niranjan B</pubmed_authors><pubmed_authors>Daly RJ</pubmed_authors><pubmed_authors>Clark KC</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proteomic characterisation of prostate cancer intercellular communication reveals cell type-selective signalling and TMSB4X-dependent fibroblast reprogramming.</name><description>&lt;h4>Background&lt;/h4>In prostate cancer, the tumour microenvironment (TME) represents an important regulator of disease progression and response to treatment. In the TME, cancer-associated fibroblasts (CAFs) play a key role in tumour progression, however the mechanisms underpinning fibroblast-cancer cell interactions are incompletely resolved. Here, we address this by applying cell type-specific labelling with amino acid precursors (CTAP) and mass spectrometry (MS)-based (phospho)proteomics to prostate cancer for the first time.&lt;h4>Methods&lt;/h4>Reciprocal interactions between PC3 prostate cancer cells co-cultured with WPMY-1 prostatic fibroblasts were characterised using CTAP-MS. Signalling network changes were determined using Metascape and Enrichr and visualised using Cytoscape. Thymosin β4</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-07-14T15:28:49.435Z</modification><creation>2025-04-07T07:04:04.31Z</creation></dates><accession>S-EPMC9747870</accession><cross_references><pubmed>36169805</pubmed><doi>10.1007/s13402-022-00719-z</doi></cross_references></HashMap>