PMID- 23470460 OWN - NLM STAT- MEDLINE DCOM- 20130702 LR - 20130506 IS - 1096-0945 (Electronic) IS - 0014-4800 (Linking) VI - 94 IP - 3 DP - 2013 Jun TI - Expression analysis of thrombospondin 2 in prostate cancer and benign prostatic hyperplasia. PG - 438-44 LID - S0014-4800(13)00032-4 [pii] LID - 10.1016/j.yexmp.2013.02.002 [doi] AB - Thrombospondin 2 (TSP2) is a protein with important roles in different tumor types, mainly related to tumor inhibition. However, there are limiting data regarding TSP2 in prostate cancer (PCa) and benign prostatic hyperplasia (BPH). We aimed to investigate TSP2 transcript and protein expression in tumoral and non-tumoral prostate tissues and cell lines, and its implications for PCa diagnosis and progression. TSP2 transcript expression was evaluated by real time PCR in PCa and BPH tissue samples and in tumoral and non-tumoral cell lines. TSP2 protein expression analysis was conducted by immunohistochemistry in a tissue microarray (TMA) containing PCa and BPH tissue samples. TSP2 transcript was down-regulated in PCa tissue samples and cell lines, when compared to BPH and non-tumoral samples (P<0.01). Receiver Operating Curve (ROC) analysis demonstrated that TSP2 transcript levels can better distinguish PCa from BPH tissue samples (P<0.01) than serum PSA levels (P=0.299). TSP2 protein expression has been observed in the cytoplasm of both PCa and BPH epithelial and stromal compartments. TSP2 stromal staining scores were significantly lower in PCa than in BPH tissues (P<0.01), while similar TSP2 epithelial staining patterns were observed in both diseases. Notably, the TSP2 epithelial staining score was significantly correlated to vascular invasion and biochemical recurrence in PCa tissue samples (P<0.05). Our data indicate that TSP2 is down-regulated at PCa tissues and cell lines, especially at stroma compartment, which could be related to PCa progression. TSP2 levels could potentially be applied for differential PCa and BPH diagnosis. CI - Copyright (c) 2013 Elsevier Inc. All rights reserved. FAU - Matos, A R AU - Matos AR AD - Programa de Carcinogenese Molecular/Programa de Pos Graduacao Stricto Sensu em Oncologia do Instituto Nacional de Cancer, CPQ, Rio de Janeiro, RJ, Brazil. FAU - Coutinho-Camillo, C M AU - Coutinho-Camillo CM FAU - Thuler, L C S AU - Thuler LC FAU - Fonseca, F P AU - Fonseca FP FAU - Soares, F A AU - Soares FA FAU - Silva, E A AU - Silva EA FAU - Gimba, E R AU - Gimba ER LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20130305 PL - Netherlands TA - Exp Mol Pathol JT - Experimental and molecular pathology JID - 0370711 RN - 0 (DNA, Neoplasm) RN - 0 (Thrombospondins) RN - 0 (thrombospondin 2) RN - EC 3.4.21.77 (Prostate-Specific Antigen) SB - IM MH - Adenocarcinoma/*genetics/metabolism/pathology MH - Cell Line, Tumor MH - DNA, Neoplasm/analysis MH - Disease Progression MH - Down-Regulation MH - Epithelial Cells/metabolism/pathology MH - *Gene Expression Regulation, Neoplastic MH - Humans MH - Immunohistochemistry/methods MH - Male MH - Predictive Value of Tests MH - Prostate-Specific Antigen/blood MH - Prostatic Hyperplasia/*genetics/metabolism/pathology MH - Prostatic Neoplasms/*genetics/metabolism/pathology MH - ROC Curve MH - Real-Time Polymerase Chain Reaction MH - Stromal Cells/metabolism/pathology MH - Thrombospondins/*genetics/metabolism MH - Tissue Array Analysis EDAT- 2013/03/09 06:00 MHDA- 2013/07/03 06:00 CRDT- 2013/03/09 06:00 PHST- 2012/10/20 00:00 [received] PHST- 2013/02/18 00:00 [revised] PHST- 2013/02/22 00:00 [accepted] PHST- 2013/03/09 06:00 [entrez] PHST- 2013/03/09 06:00 [pubmed] PHST- 2013/07/03 06:00 [medline] AID - S0014-4800(13)00032-4 [pii] AID - 10.1016/j.yexmp.2013.02.002 [doi] PST - ppublish SO - Exp Mol Pathol. 2013 Jun;94(3):438-44. doi: 10.1016/j.yexmp.2013.02.002. Epub 2013 Mar 5.