Gs indicate that HIST1H4L is a potential target of

Gs indicate that HIST1H4L is a potential target of ERG fusion genes, as also illustrated by our demonstration of direct binding of ERG to the HIST1H4L promoter, but the mechanism whereby it is involved in prostate carcinogenesis is still unknown. KCNN2 codes for a small conductance Ca2+-activated potassium channel involved in the regulation of the neuronal excitability [55], and, to our knowledge, we here show for the first time that this gene is BTZ-043 overexpressed in PCa harboring ERG rearrangements when compared to the other subtypes of PCa and to NPT. On the other hand, KCNN2 was underexpressed in both PCa with other ETS rearrangements and in those without ETS rearrangements when compared to NPT. These data suggest that KCNN2 regulation may be mediated by the aberrant ERG transcription factor in a particular subtype of PCa (PCa ERG+), as also illustrated by our demonstration of direct binding of ERG to the KCNN2 promoter, and that different ETS can have specific roles, even in the same cellular context. Conversely, we show for the first time that KCNN2 is significantly underexpressed in ESFT when compared to ARMS. Since it has been previously shown that EWSR1-FLI1 binds to the promoter of KCNN2 in vitro [20], it seems reasonable to assume that this downregulation of KCNN2 in ESFT might be directly mediated by the chimeric transcription factor. On the other hand, although HIST1H4L was also found as a direct target of the EWSR1-FLI1 chimeric protein [20], our data showed that the expression of HIST1H4L was not significantly different between the ESFT and ARMS, thus suggesting that either EWSR1-FLI1 does not regulate HIST1H4L expression in vivo or that other regulatory mechanism in ARMS is regulating HIST1H4L to similar expression levels. In conclusion, using two different models of ETS-related tumors, we show that, despite of the conservation of the DNA binding domain of the ETS family of transcription factors, ETS proteins can modulate common target genes in different manners, as well as achieve specificity by controlling distinct genes.Supporting InformationFigure S1 Comparative methylation and expression levels of CAV1 after DAC treatment of LNCaP and 22Rv1 prostate cancer cell lines. (TIF) Table S1 Assay ID or sequence of the primers used inthis study. (DOC)Table S2 MSP analysis data of prostate samples.(DOC)ETS Fusion Targets in CancerAuthor ContributionsConceived and designed the experiments: MRT. Performed the experiments: MJC PP JDBS MA VLC. Analyzed the data: MJC PP FRR.Contributed reagents/materials/analysis tools: NC RIS RAL RH CJ. Wrote the paper: 1407003 MRT PP.
Wilson’s disease is an autosomal CASIN recessively inherited disorder that leads to copper accumulation and, consequently, to hepatic damage and neuropsychological symptoms [1,2]. The causative mutations affect the copper-transporting P-type ATPase ATP7B, which regulates the hepatic copper metabolism, leading to impaired biliary excretion and the toxic accumulation of copper primarily in the brain and liver (reviewed in [3] and [4]). Intracellular copper deposits impede inhibitor of apoptosis proteins (IAPs), which eventually causes apoptotic cell death [5]. The clinical presentation varies from predominantly hepatic to predominantly neurologic and shows great heterogeneity regarding severity, age of onset and initial symptoms [6]. Wilson’s disease results in severe disability and death if untreated. The key neurological features comprise extrapyramidal symptoms, ataxia, dystonia, sei.Gs indicate that HIST1H4L is a potential target of ERG fusion genes, as also illustrated by our demonstration of direct binding of ERG to the HIST1H4L promoter, but the mechanism whereby it is involved in prostate carcinogenesis is still unknown. KCNN2 codes for a small conductance Ca2+-activated potassium channel involved in the regulation of the neuronal excitability [55], and, to our knowledge, we here show for the first time that this gene is overexpressed in PCa harboring ERG rearrangements when compared to the other subtypes of PCa and to NPT. On the other hand, KCNN2 was underexpressed in both PCa with other ETS rearrangements and in those without ETS rearrangements when compared to NPT. These data suggest that KCNN2 regulation may be mediated by the aberrant ERG transcription factor in a particular subtype of PCa (PCa ERG+), as also illustrated by our demonstration of direct binding of ERG to the KCNN2 promoter, and that different ETS can have specific roles, even in the same cellular context. Conversely, we show for the first time that KCNN2 is significantly underexpressed in ESFT when compared to ARMS. Since it has been previously shown that EWSR1-FLI1 binds to the promoter of KCNN2 in vitro [20], it seems reasonable to assume that this downregulation of KCNN2 in ESFT might be directly mediated by the chimeric transcription factor. On the other hand, although HIST1H4L was also found as a direct target of the EWSR1-FLI1 chimeric protein [20], our data showed that the expression of HIST1H4L was not significantly different between the ESFT and ARMS, thus suggesting that either EWSR1-FLI1 does not regulate HIST1H4L expression in vivo or that other regulatory mechanism in ARMS is regulating HIST1H4L to similar expression levels. In conclusion, using two different models of ETS-related tumors, we show that, despite of the conservation of the DNA binding domain of the ETS family of transcription factors, ETS proteins can modulate common target genes in different manners, as well as achieve specificity by controlling distinct genes.Supporting InformationFigure S1 Comparative methylation and expression levels of CAV1 after DAC treatment of LNCaP and 22Rv1 prostate cancer cell lines. (TIF) Table S1 Assay ID or sequence of the primers used inthis study. (DOC)Table S2 MSP analysis data of prostate samples.(DOC)ETS Fusion Targets in CancerAuthor ContributionsConceived and designed the experiments: MRT. Performed the experiments: MJC PP JDBS MA VLC. Analyzed the data: MJC PP FRR.Contributed reagents/materials/analysis tools: NC RIS RAL RH CJ. Wrote the paper: 1407003 MRT PP.
Wilson’s disease is an autosomal recessively inherited disorder that leads to copper accumulation and, consequently, to hepatic damage and neuropsychological symptoms [1,2]. The causative mutations affect the copper-transporting P-type ATPase ATP7B, which regulates the hepatic copper metabolism, leading to impaired biliary excretion and the toxic accumulation of copper primarily in the brain and liver (reviewed in [3] and [4]). Intracellular copper deposits impede inhibitor of apoptosis proteins (IAPs), which eventually causes apoptotic cell death [5]. The clinical presentation varies from predominantly hepatic to predominantly neurologic and shows great heterogeneity regarding severity, age of onset and initial symptoms [6]. Wilson’s disease results in severe disability and death if untreated. The key neurological features comprise extrapyramidal symptoms, ataxia, dystonia, sei.