Department of Urology, Nara Medical University, 840 Shijo-cho, Nara 634-8522, Japan.
Department of Pathology, Nara Medical University, 840 Shijo-cho, Nara 634-8522, Japan.
Int J Mol Sci. 2020 May 27;21(11):3789. doi: 10.3390/ijms21113789.
Heparan sulfate proteoglycan syndecan-1, CD138, is known to be associated with cell proliferation, adhesion, and migration in malignancies. We previously reported that syndecan-1 (CD138) may contribute to urothelial carcinoma cell survival and progression. We investigated the role of heparanase, an enzyme activated by syndecan-1 in human urothelial carcinoma. Using human urothelial cancer cell lines, MGH-U3 and T24, heparanase expression was reduced with siRNA and RK-682, a heparanase inhibitor, to examine changes in cell proliferation activity, induction of apoptosis, invasion ability of cells, and its relationship to autophagy. A bladder cancer development mouse model was treated with RK-682 and the bladder tissues were examined using immunohistochemical analysis for Ki-67, E-cadherin, LC3, and CD31 expressions. Heparanase inhibition suppressed cellular growth by approximately 40% and induced apoptosis. The heparanase inhibitor decreased cell activity in a concentration-dependent manner and suppressed invasion ability by 40%. Inhibition of heparanase was found to suppress autophagy. In N-butyl-N-(4-hydroxybutyl) nitrosamine (BBN)-induced bladder cancer mice, treatment with heparanase inhibitor suppressed the progression of cancer by 40%, compared to controls. Immunohistochemistry analysis showed that heparanase inhibitor suppressed cell growth, and autophagy. In conclusion, heparanase suppresses apoptosis and promotes invasion and autophagy in urothelial cancer.
硫酸乙酰肝素蛋白聚糖连接蛋白-1(syndecan-1,CD138)已知与恶性肿瘤中的细胞增殖、黏附和迁移有关。我们之前报道过,syndecan-1(CD138)可能有助于尿路上皮癌细胞的存活和进展。我们研究了肝素酶在人类尿路上皮癌中的作用,肝素酶是一种由 syndecan-1 激活的酶。使用人尿路上皮癌细胞系 MGH-U3 和 T24,用 siRNA 和肝素酶抑制剂 RK-682 降低 heparanase 的表达,以研究细胞增殖活性、细胞凋亡诱导、细胞侵袭能力的变化及其与自噬的关系。用 RK-682 处理膀胱癌发展的小鼠模型,并通过免疫组织化学分析检测膀胱组织中 Ki-67、E-cadherin、LC3 和 CD31 的表达。肝素酶抑制可使细胞生长抑制约 40%,并诱导细胞凋亡。肝素酶抑制剂以浓度依赖的方式降低细胞活性,抑制侵袭能力达 40%。发现肝素酶抑制可抑制自噬。在 N-丁基-N-(4-羟丁基)亚硝胺(BBN)诱导的膀胱癌小鼠中,与对照组相比,肝素酶抑制剂治疗可抑制癌症进展 40%。免疫组织化学分析表明,肝素酶抑制剂抑制细胞生长和自噬。总之,肝素酶抑制尿路上皮癌中的细胞凋亡,并促进其侵袭和自噬。