Potential Downstream Target Genes of Aberrant ETS Transcription Factors Are Differentially Affected in Ewing's Sarcoma and Prostate Carcinoma

被引:15
作者
Camoes, Maria J. [1 ,2 ]
Paulo, Paula [1 ,2 ]
Ribeiro, Franclim R. [1 ,2 ]
Barros-Silva, Joao D. [1 ,2 ]
Almeida, Mafalda [1 ,3 ]
Costa, Vera L. [1 ,3 ]
Cerveira, Nuno [1 ,2 ]
Skotheim, Rolf I. [4 ,5 ]
Lothe, Ragnhild A. [4 ,5 ]
Henrique, Rui [3 ,6 ,7 ]
Jeronimo, Carmen [1 ,3 ,7 ]
Teixeira, Manuel R. [1 ,2 ,5 ,7 ]
机构
[1] Portuguese Oncol Inst Porto, Dept Genet, Oporto, Portugal
[2] Portuguese Oncol Inst Porto, Res Ctr, Canc Genet Grp, Oporto, Portugal
[3] Portuguese Oncol Inst, Canc Epigenet Grp, Res Ctr, Oporto, Portugal
[4] Oslo Univ Hosp, Norwegian Radium Hosp, Inst Canc Res, Dept Canc Prevent, Oslo, Norway
[5] Univ Oslo, Fac Med, Ctr Canc Biomed, Oslo, Norway
[6] Portuguese Oncol Inst Porto, Dept Pathol, Oporto, Portugal
[7] Univ Porto, Inst Biomed Sci Abel Salazar ICBAS, Dept Pathol & Mol Immunol, P-4100 Oporto, Portugal
关键词
NUCLEAR RECEPTOR DAX1; RESPONSE ELEMENTS; IN-VITRO; TRANSFORMING GENE; TGF-BETA; CANCER; FAMILY; FUSION; EWS/FLI-1; TMPRSS2;
D O I
10.1371/journal.pone.0049819
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
FLI1 and ERG, the major ETS transcription factors involved in rearrangements in the Ewing's sarcoma family of tumors (ESFT) and in prostate carcinomas (PCa), respectively, belong to the same subfamily, having 98% sequence identity in the DNA binding domain. We therefore decided to investigate whether the aberrant transcription factors in both malignancies have some common downstream targets. We crossed a publicly available list of all putative EWSR1-FLI1 target genes in ESFT with our microarray expression data on 24 PCa and 6 non-malignant prostate tissues (NPT) and choose four genes among the top-most differentially expressed between PCa with (PCa ERG+) and without (PCa ETS-) ETS fusion genes (HIST1H4L, KCNN2, ECRG4 and LDOC1), as well as four well-validated direct targets of the EWSR1-FLI1 chimeric protein in ESFT (NR0B1, CAV1, IGFBP3 and TGFBR2). Using quantitative expression analysis in 16 ESFT and seven alveolar rhabdomyosarcomas (ARMS), we were able to validate the four genes previously described as direct targets of the EWSR1-FLI1 oncoprotein, showing overexpression of CAV1 and NR0B1 and underexpression of IGFBP3 and TGFBR2 in ESFT as compared to ARMS. Although none of these four genes showed significant expression differences between PCa ERG+ and PCa ETS-, CAV1, IGFBP3 and TGFBR2 were less expressed in PCa in an independent series of 56 PCa and 15 NPT, as also observed for ECRG4 and LDOC1, suggesting a role in prostate carcinogenesis in general. On the other hand, we demonstrate for the first time that both HIST1H4L and KCNN2 are significantly overexpressed in PCa ERG+ and that ERG binds to the promoter of these genes. Conversely, KCNN2 was found underexpressed in ESFT relative to ARMS, suggesting that the EWSR1-ETS oncoprotein may have the opposite effect of ERG rearrangements in PCa. We conclude that aberrant ETS transcription factors modulate target genes differently in ESFT and PCa.
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页数:9
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