Department of Surgery, Union Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei Province, China.
PLoS One. 2012;7(2):e31379. doi: 10.1371/journal.pone.0031379. Epub 2012 Feb 20.
Heparanase (HPA), an endo-h-D-glucuronidase that cleaves the heparan sulfate chain of heparan sulfate proteoglycans, is overexpressed in majority of human cancers. Recent evidence suggests that small interfering RNA (siRNA) induces transcriptional gene silencing (TGS) in human cells. In this study, transfection of siRNA against -9/+10 bp (siH3), but not -174/-155 bp (siH1) or -134/-115 bp (siH2) region relative to transcription start site (TSS) locating at 101 bp upstream of the translation start site, resulted in TGS of heparanase in human prostate cancer, bladder cancer, and gastric cancer cells in a sequence-specific manner. Methylation-specific PCR and bisulfite sequencing revealed no DNA methylation of CpG islands within heparanase promoter in siH3-transfected cells. The TGS of heparanase did not involve changes of epigenetic markers histone H3 lysine 9 dimethylation (H3K9me2), histone H3 lysine 27 trimethylation (H3K27me3) or active chromatin marker acetylated histone H3 (AcH3). The regulation of alternative splicing was not involved in siH3-mediated TGS. Instead, siH3 interfered with transcription initiation via decreasing the binding of both RNA polymerase II and transcription factor II B (TFIIB), but not the binding of transcription factors Sp1 or early growth response 1, on the heparanase promoter. Moreover, Argonaute 1 and Argonaute 2 facilitated the decreased binding of RNA polymerase II and TFIIB on heparanase promoter, and were necessary in siH3-induced TGS of heparanase. Stable transfection of the short hairpin RNA construct targeting heparanase TSS (-9/+10 bp) into cancer cells, resulted in decreased proliferation, invasion, metastasis and angiogenesis of cancer cells in vitro and in athymic mice models. These results suggest that small RNAs targeting TSS can induce TGS of heparanase via interference with transcription initiation, and significantly suppress the tumor growth, invasion, metastasis and angiogenesis of cancer cells.
乙酰肝素酶(HPA)是一种内切糖苷酶,能够裂解乙酰肝素硫酸链的乙酰肝素硫酸蛋白聚糖,在大多数人类癌症中过度表达。最近的证据表明,小干扰 RNA(siRNA)可诱导人类细胞中的转录基因沉默(TGS)。在这项研究中,相对于转录起始位点(TSS)位于翻译起始位点上游 101bp 的位置,转染针对-9/+10bp(siH3)而非-174/-155bp(siH1)或-134/-115bp(siH2)区域的 siRNA 导致人前列腺癌、膀胱癌和胃癌细胞中乙酰肝素酶的 TGS 以序列特异性方式发生。甲基化特异性 PCR 和亚硫酸氢盐测序显示,在 siH3 转染的细胞中,乙酰肝素酶启动子内的 CpG 岛没有 DNA 甲基化。乙酰肝素酶的 TGS 不涉及表观遗传标记组蛋白 H3 赖氨酸 9 二甲基化(H3K9me2)、组蛋白 H3 赖氨酸 27 三甲基化(H3K27me3)或活性染色质标记乙酰化组蛋白 H3(AcH3)的变化。替代剪接的调节不涉及 siH3 介导的 TGS。相反,siH3 通过减少 RNA 聚合酶 II 和转录因子 II B(TFIIB)的结合来干扰转录起始,但不影响转录因子 Sp1 或早期生长反应 1 与乙酰肝素酶启动子的结合。此外,Argonaute 1 和 Argonaute 2 促进了 RNA 聚合酶 II 和 TFIIB 在乙酰肝素酶启动子上的结合减少,并且是 siH3 诱导的乙酰肝素酶 TGS 所必需的。靶向乙酰肝素酶 TSS(-9/+10bp)的短发夹 RNA 构建体的稳定转染到癌细胞中,导致体外和裸鼠模型中癌细胞的增殖、侵袭、转移和血管生成减少。这些结果表明,靶向 TSS 的小 RNA 可以通过干扰转录起始来诱导乙酰肝素酶的 TGS,并显著抑制癌细胞的肿瘤生长、侵袭、转移和血管生成。