Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville 41013, Spain.
Cell Death Dis. 2013 Apr 4;4(4):e576. doi: 10.1038/cddis.2013.90.
PTPL1 is a non-receptor protein tyrosine phosphatase involved in apoptosis regulation, although controversial findings have been reported in different cancer types. We report here a proapoptotic role for PTPL1 in PC3 and LNCaP prostate cancer cells, as its absence induces apoptosis resistance upon treatment with different drugs. In PC3 cells, PTPL1 silencing by small interfering RNA influences the expression levels of Bcl-xL and Mcl-1(S) proteins as well as final events in the apoptotic process such as activation of caspases and caspase-mediated cleavage of proteins like Mcl-1 or poly (ADP-ribose) polymerase. We have identified PKCδ as an intermediary of PTPL1-mediated apoptotic signalling and that phosphorylation status of NF-κB and IκBα is influenced by PTPL1 and PKCδ. Furthermore, the loss of PTPL1 and PKCδ expression in poorly differentiated, more aggressive human prostate cancers also indicate that their absence could be related to apoptosis resistance and tumour progression.
PTPL1 是一种非受体蛋白酪氨酸磷酸酶,参与细胞凋亡的调控,但在不同类型的癌症中,其作用存在争议。我们在此报告,PTPL1 在前列腺癌细胞 PC3 和 LNCaP 中发挥促凋亡作用,因为其缺失会导致细胞对不同药物的治疗产生抗凋亡作用。在 PC3 细胞中,小干扰 RNA 沉默 PTPL1 会影响 Bcl-xL 和 Mcl-1(S) 蛋白的表达水平,以及凋亡过程中的终末事件,如半胱天冬酶的激活以及 caspase 介导的 Mcl-1 或多聚(ADP-核糖)聚合酶的切割。我们已经确定 PKCδ 是 PTPL1 介导的凋亡信号通路的中间介质,并且 NF-κB 和 IκBα 的磷酸化状态受到 PTPL1 和 PKCδ 的影响。此外,在分化不良、侵袭性更强的人类前列腺癌中,PTPL1 和 PKCδ 的缺失表达也表明,它们的缺失可能与细胞凋亡抵抗和肿瘤进展有关。