Pannuru Padmavathi, Dontula Ranadheer, Khan Anwar A, Herbert Englehard, Ozer Howard, Chetty Chandramu, Lakka Sajani S
From the Section of Hematology/Oncology, University of Illinois Cancer Center, College of Medicine at Chicago, Chicago, IL 60612, USA.
Department of Neurosurgery, University of Illinois, College of Medicine at Chicago, Chicago, IL 60612, USA.
Cell Signal. 2014 Oct;26(10):2193-201. doi: 10.1016/j.cellsig.2014.06.014. Epub 2014 Jul 8.
Our previous studies indicate that Secreted Protein Acidic and Rich in Cysteine (SPARC) expression suppressed medulloblastoma tumor growth in vitro and in vivo. Here we sought to determine the effect of SPARC expression in medulloblastoma cells to chemotherapeutic agents. In this study, we show that SPARC expression induces cisplatin resistance in medulloblastoma cells. We also demonstrate that the autophagy was involved in SPARC expression mediated resistance to cisplatin. Suppression of autophagy by either autophagy inhibitor, 3-methyladenosine (3MA) or Atg5 siRNA enhanced cisplatin sensitivity in SPARC expressed cells. Further, SPARC expression suppressed miR-let-7f-1 expression which resulted in disrupted repression of High Mobility Group Box 1 (HMGB1), a critical regulator of autophagy. We also show that HMGB1 is a direct target of miR-let-7f-1 and forced expression of HMGB1 cDNA enhanced cisplatin sensitivity in SPARC expressed cells. In summary, our results suggest that SPARC modulates cisplatin resistance by modulating the Let-7f-1 miRNA/HMGB1 axis in medulloblastoma cells.
我们之前的研究表明,富含半胱氨酸的酸性分泌蛋白(SPARC)的表达在体外和体内均能抑制髓母细胞瘤的肿瘤生长。在此,我们试图确定SPARC在髓母细胞瘤细胞中表达对化疗药物的影响。在本研究中,我们发现SPARC的表达可诱导髓母细胞瘤细胞产生顺铂耐药性。我们还证明自噬参与了SPARC表达介导的顺铂耐药性。通过自噬抑制剂3-甲基腺嘌呤(3MA)或Atg5小干扰RNA(siRNA)抑制自噬,可增强SPARC表达细胞对顺铂的敏感性。此外,SPARC的表达抑制了微小RNA let-7f-1的表达,从而导致对自噬关键调节因子高迁移率族蛋白B1(HMGB1)的抑制作用被破坏。我们还表明HMGB1是miR-let-7f-1的直接靶点,在SPARC表达细胞中强制表达HMGB1 cDNA可增强顺铂敏感性。总之,我们的结果表明,SPARC通过调节髓母细胞瘤细胞中的Let-7f-1微小RNA/HMGB1轴来调节顺铂耐药性。