Mazumdar Tapati, DeVecchio Jennifer, Agyeman Akwasi, Shi Ting, Houghton Janet A
Department of Cancer Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
Oncotarget. 2011 Aug;2(8):638-45. doi: 10.18632/oncotarget.310.
The Hedgehog (HH) signaling pathway leads to activation of GLI, which transcriptionally regulate target genes. Regulated HH signaling activity is critical during embryogenesis while aberrantly activated HH signaling is evident in a variety of human cancers. Canonical HH signaling engages the transmembrane receptor Patched (PTCH) and the signaling intermediate Smoothened (SMO) to activate GLI1 and GLI2. In addition GLI1 and GLI2 are activated by non-canonical oncogenic signaling pathways to further drive HH-dependent survival. We have demonstrated in human colon carcinoma cells that inhibition of the RAS/RAF pathway by U0126 decreases p-ERK protein expression and also inhibits GLI-luciferase activity and GLI1 mRNA and protein levels. Of importance is the demonstration that targeting of SMO (using cyclopamine) has minimal effect on cell survival in comparison to the inhibition of GLI (using GANT61), which induced extensive cell death in 7/7 human colon carcinoma cell lines. Genetic inhibition of the function of GLI1 and GLI2 by transient transfection of the C-terminus deleted repressor GLI3R, reduced proliferation and induced cleavage of caspase-3 and cell death in HT29 cells, similar to the effects of GANT61. Mechanistically, downstream of GLI1 and GLI2 inhibition, γH2AX (a marker of DNA double strand breaks) expression was upregulated, and γH2AX nuclear foci were demonstrated in cells that expressed GLI3R. Activation of the ATM/Chk2 axis with co-localization of γH2AX and p-Chk2 nuclear foci were demonstrated following GLI1/GLI2 inhibition. GANT61 induced cellular accumulation at G1/S and early S with no further progression before cells became subG1, while cDNA microarray gene profiling demonstrated downregulation of genes involved in DNA replication, the DNA damage response, and DNA repair, mechanisms that are currently being pursued. These studies highlight the importance of targeting the GLI genes downstream of SMO for terminating HH-dependent survival, suggesting that GLI may constitute a molecular switch that determines the balance between cell survival and cell death in human colon carcinoma.
刺猬信号通路(HH)可导致GLI激活,进而对靶基因进行转录调控。在胚胎发育过程中,HH信号活性的调控至关重要,而在多种人类癌症中,HH信号异常激活的现象十分明显。经典的HH信号通路通过跨膜受体Patched(PTCH)和信号中间体Smoothened(SMO)来激活GLI1和GLI2。此外,GLI1和GLI2还可被非经典致癌信号通路激活,从而进一步促进HH依赖的细胞存活。我们在人结肠癌细胞中证实,U0126对RAS/RAF通路的抑制可降低p-ERK蛋白表达,同时抑制GLI荧光素酶活性以及GLI1 mRNA和蛋白水平。重要的是,与抑制GLI(使用GANT61)相比,靶向SMO(使用环杷明)对细胞存活的影响极小,GANT61可在7种人结肠癌细胞系中诱导广泛的细胞死亡。通过瞬时转染C端缺失的阻遏物GLI3R对GLI1和GLI2功能进行基因抑制,可降低HT29细胞的增殖,并诱导caspase-3的切割和细胞死亡,这与GANT61的作用效果相似。从机制上来说,在抑制GLI1和GLI2之后,γH2AX(DNA双链断裂的标志物)的表达上调,并且在表达GLI3R的细胞中观察到了γH2AX核灶。在抑制GLI1/GLI2之后,证实了ATM/Chk2轴的激活以及γH2AX和p-Chk2核灶的共定位。GANT61诱导细胞在G1/S期和早期S期积累,在细胞进入亚G1期之前不再进一步进展,而cDNA微阵列基因谱分析显示参与DNA复制、DNA损伤反应和DNA修复的基因下调,目前正在对这些机制进行研究。这些研究突出了靶向SMO下游的GLI基因对于终止HH依赖的细胞存活的重要性,表明GLI可能构成一个分子开关,决定人结肠癌中细胞存活与细胞死亡之间的平衡。