<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lin HP</submitter><funding>NCI NIH HHS</funding><pagination>e82625</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3857776</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(12)</volume><pubmed_abstract>Androgen ablation therapy is the primary treatment for metastatic prostate cancer. However, 80-90% of the patients who receive androgen ablation therapy ultimately develop recurrent tumors in 12-33 months after treatment with a median overall survival time of 1-2 years after relapse. LNCaP is a commonly used cell line established from a human lymph node metastatic lesion of prostatic adenocarcinoma. We previously established two relapsed androgen receptor (AR)-rich androgen-independent LNCaP sublines 104-R1 (androgen depleted for 12 months) and 104-R2 cells (androgen depleted for 24 months) from AR-positive androgen-dependent LNCaP 104-S cells. LNCaP 104-R1 and 104-R2 mimics the AR-positive hormone-refractory relapsed tumors in patients receiving androgen ablation therapy. Androgen treatme</pubmed_abstract><journal>PloS one</journal><pubmed_title>Difference in protein expression profile and chemotherapy drugs response of different progression stages of LNCaP sublines and other human prostate cancer cells.</pubmed_title><pmcid>PMC3857776</pmcid><funding_grant_id>P30 CA093373</funding_grant_id><pubmed_authors>Chen M</pubmed_authors><pubmed_authors>Chuu CP</pubmed_authors><pubmed_authors>Wang HD</pubmed_authors><pubmed_authors>Kung HJ</pubmed_authors><pubmed_authors>Hsiao PH</pubmed_authors><pubmed_authors>Lin HP</pubmed_authors><pubmed_authors>Jiang SS</pubmed_authors><pubmed_authors>Hsu JM</pubmed_authors><pubmed_authors>Lin CY</pubmed_authors><pubmed_authors>Jim WT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Difference in protein expression profile and chemotherapy drugs response of different progression stages of LNCaP sublines and other human prostate cancer cells.</name><description>Androgen ablation therapy is the primary treatment for metastatic prostate cancer. However, 80-90% of the patients who receive androgen ablation therapy ultimately develop recurrent tumors in 12-33 months after treatment with a median overall survival time of 1-2 years after relapse. LNCaP is a commonly used cell line established from a human lymph node metastatic lesion of prostatic adenocarcinoma. We previously established two relapsed androgen receptor (AR)-rich androgen-independent LNCaP sublines 104-R1 (androgen depleted for 12 months) and 104-R2 cells (androgen depleted for 24 months) from AR-positive androgen-dependent LNCaP 104-S cells. LNCaP 104-R1 and 104-R2 mimics the AR-positive hormone-refractory relapsed tumors in patients receiving androgen ablation therapy. Androgen treatme</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013</publication><modification>2025-04-04T20:50:57.971Z</modification><creation>2019-03-26T23:17:17Z</creation></dates><accession>S-EPMC3857776</accession><cross_references><pubmed>24349321</pubmed><doi>10.1371/journal.pone.0082625</doi></cross_references></HashMap>