<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Biostatistics, Ducan Cancer Center, Baylor College of Medicine</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA224104</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>Prostate stroma-specific TGF-beta signaling induces morphological changes in LNCaP cells. We have previously shown that stromal TGF-beta signaling regulates prostate tumor growth. To further delineate the underlying mechanisms, we generated LNCaP cells overexpressing an HA-tagged constitutively activate TGF-beta1 ligand (LNCaP-HA-TGF-β1(a)) and control LNCaP cells (LNCaP-Ctrl), and performed in vitro co-cultures of LNCaP-HA-TGF-β1(a) and LNCaP-Ctrl cells on top of the confluent HPS-19I cells, a human prostate stromal cell line. Since LNCaP cells are defective in TGF-beta receptor I (TbetaRI / ALK-5) that is essential for mediating TGF-beta signaling, only HPS19I cells are able to respond to TGF-beta ligand in these co-cultures. This provides a unique opportunity to study how prostate stromal cell-specific TGF-beta signaling regulates PCa biology. Overall design: LNCaP + HPS19I co-cultures, with or without TGF-beta and with or without SD208 (a TBetaRI (ALK-5) protein kinase-specific inhibitor) KEYWORDS: multiple group comparison</long_description><tag>xref:PubMed:25333263</tag><repository>ENA</repository><name_synonyms>Human, Modern., human being, Man (Taxonomy), Homo sapiens, man, Man, human, Modern Man</name_synonyms><description_synonyms>signalling., hereditary prostate cancer, l(3)j5A5, cancer of the prostate, biological signaling, Cocultures, Coculture Technique, ho, Tgf-r, pun, TGF-b, Prostate Neoplasms, Punt, Neoplasms, M(2)LS1, familial, TGF-beta5, TGF-beta, Tg, Bone-Derived Transforming Growth Factor, AtrII, Act-r, CG9885, Factor, DPP-C, lap, Cell, CG7904, TGFbeta, Milk, Bone Derived Transforming Growth Factor, tgfbeta, Milk Growth Factor, Hin-d, Milk Growth, DmelCG9885, Atr88CD, Atr-II, l(2)22Fa, Prostatic Cancer, PUNT, DmelCG7904, Neoplasm, Prostatic Cancers, Cocultivation, NOS, Growth Factor, tgfb5, Cocultivations, l(3)10460, Cancer of Prostate, Co-culture, Prostate Cancers, Dm-DPP, l(2)k17036, shv, Coculture, ced, Dpp, DPP, transforming growth factor beta, Co-cultures, tgf-beta, M(2)23AB, l(2)10638, dlhC, Platelet Transforming Growth Factor, Cancers, tgfb, cancer of prostate, Prostate Neoplasm, blk, Prostatic Neoplasm, BMP, Cancer of the Prostate, signalling process, TGF-B, signaling process, Put, Prostatic, prostate cancer, atrII, PC, dpd1, Co culture, STK-C, Prostate Cancer, Prostate, stromal connective tissue, Atr, single organism signaling, Cancer</description_synonyms></additional><is_claimable>false</is_claimable><name>Homo sapiens</name><description>Expression profiling of co-cultures of prostate cancer cells and stroma cells, with or without TGF-beta signaling</description><dates><last_updated>2025-09-24</last_updated><first_public>2014-11-13</first_public></dates><accession>PRJNA224104</accession><cross_references><GEO>GSE51617</GEO><taxon>9606</taxon><PubMed>25333263</PubMed></cross_references></HashMap>