Carnesecchi Julie, Cerutti Catherine, Vanacker Jean-Marc, Forcet Christelle
Institut de Génomique Fonctionnelle de Lyon, Université de Lyon, Université Lyon I, CNRS UMR5242, Ecole Normale Supérieure de Lyon, Lyon, France.
PLoS One. 2017 Nov 30;12(11):e0188871. doi: 10.1371/journal.pone.0188871. eCollection 2017.
The LSD1 histone demethylase is highly expressed in breast tumors where it constitutes a factor of poor prognosis and promotes traits of cancer aggressiveness such as cell invasiveness. Recent work has shown that the Estrogen-Related Receptor α (ERRα) induces LSD1 to demethylate the Lys 9 of histone H3. This results in the transcriptional activation of a number of common target genes, several of which being involved in cellular invasion. High expression of ERRα protein is also a factor of poor prognosis in breast tumors. Here we show that, independently of its demethylase activities, LSD1 protects ERRα from ubiquitination, resulting in overexpression of the latter protein. Our data also suggests that the elevation of LSD1 mRNA and protein in breast cancer (as compared to normal tissue) may be a key event to increase ERRα protein, independently of its corresponding mRNA.
赖氨酸特异性去甲基化酶1(LSD1)在乳腺肿瘤中高表达,它是预后不良的一个因素,并促进癌症侵袭性特征,如细胞侵袭。最近的研究表明,雌激素相关受体α(ERRα)诱导LSD1使组蛋白H3的赖氨酸9去甲基化。这导致许多共同靶基因的转录激活,其中一些与细胞侵袭有关。ERRα蛋白的高表达也是乳腺肿瘤预后不良的一个因素。在这里,我们表明,独立于其去甲基酶活性,LSD1保护ERRα不被泛素化,导致后者蛋白的过表达。我们的数据还表明,乳腺癌中LSD1 mRNA和蛋白的升高(与正常组织相比)可能是增加ERRα蛋白的关键事件,与其相应的mRNA无关。