Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Avenida Manuel Siurot s/n, 41013 Seville, Spain.
Clin Exp Metastasis. 2012 Apr;29(4):349-58. doi: 10.1007/s10585-012-9455-7. Epub 2012 Jan 25.
PTPL1, a non-receptor type protein tyrosine phosphatase, has been involved in the regulation of apoptosis and invasiveness of various tumour cell types, but its role in prostate cancer remained to be investigated. We report here that downregulation of PTPL1 by small interfering RNA in PC3 cells decreases cell proliferation and concomitantly reduces the expression of cell cycle-related proteins such as cyclins E and B1, PCNA, PTTG1 and phospho-histone H3. PTPL1 downregulation also increases the invasion ability of PC3 cells through Matrigel coated membranes. cDNA array of PTPL1-silenced PC3 cells versus control cells showed an upregulation of invasion-related genes such as uPA, uPAR, tPA, PAI-1, integrin α6 and osteopontin. This increased expression was also confirmed in PTPL1-silenced DU145 prostate cancer cells by quantitative real time PCR and western blot. These findings suggest that PTPL1 is an important mediator of central cellular processes such as proliferation and invasion.
PTPL1 是一种非受体型蛋白酪氨酸磷酸酶,已被涉及调节各种肿瘤细胞类型的凋亡和侵袭性,但它在前列腺癌中的作用仍有待研究。我们在这里报告,在 PC3 细胞中通过小干扰 RNA 下调 PTPL1 会降低细胞增殖,并同时降低细胞周期相关蛋白如细胞周期蛋白 E 和 B1、PCNA、PTTG1 和磷酸化组蛋白 H3 的表达。PTPL1 下调还通过 Matrigel 包被的膜增加了 PC3 细胞的侵袭能力。与对照细胞相比,PTPL1 沉默的 PC3 细胞的 cDNA 阵列显示侵袭相关基因如 uPA、uPAR、tPA、PAI-1、整合素 α6 和骨桥蛋白的表达上调。通过定量实时 PCR 和 Western blot 在沉默 PTPL1 的 DU145 前列腺癌细胞中也证实了这种表达增加。这些发现表明,PTPL1 是增殖和侵袭等中央细胞过程的重要介质。