HSDL2 Promotes Bladder Cancer Growth In Vitro and In Vivo

被引:11
作者
Jia, Ling-Hua [1 ,2 ]
Hu, Mei-Di [3 ]
Liu, Yuan [4 ]
Xiong, Xing [2 ]
Wang, Wei-Jia [5 ]
Wang, Jin-Gen [2 ]
Li, Qiu-Gen [6 ]
机构
[1] Nanchang Univ, Jiangxi Med Coll, Grad Fac, Nanchang 330006, Jiangxi, Peoples R China
[2] Nanchang Univ, Jiangxi Prov Peoples Hosp, Dept Urol, Nanchang 330006, Jiangxi, Peoples R China
[3] Nanchang Univ, Affiliated Hosp 1, Dept Gerontol, Nanchang 330006, Jiangxi, Peoples R China
[4] Fudan Univ, Peoples Hosp Shanghai 5, Div Nephrol, Shanghai 200240, Peoples R China
[5] Nanchang Univ, Affiliated Hosp 1, Dept Pathol, Nanchang 330006, Jiangxi, Peoples R China
[6] Nanchang Univ, Jiangxi Prov Peoples Hosp, Dept Resp Med, Nanchang 330006, Jiangxi, Peoples R China
来源
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES | 2019年 / 16卷 / 05期
关键词
bladder cancer; HSDL2; shRNA; cell proliferation; apoptosis;
D O I
10.7150/ijms.31288
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bladder cancer is a common malignant urinary tumor, and patients with bladder cancer have poor prognosis. Abnormal lipid metabolism in peroxisomes is involved in tumor progression. Hydroxysteroid dehydrogenase-like 2 (HSDL2) localized in peroxisomes regulates fatty acid synthesis. In the present study, we reported that HSDL2 was upregulated in two human bladder cancer cell lines 5637 and T24 compared to normal human urothelial cells. Furthermore, lentiviral-mediated HSDL2 knockdown inhibited the proliferation and colony formation while promoted the apoptosis of human bladder cancer T24 cells in vitro. In nude mice HSDL2 knockdown inhibited the growth of T24 derived xenografts in vivo. In conclusion, our results suggest that HSDL2 plays an oncogenic role in bladder cancer and might serve as a potential target for bladder cancer therapy.
引用
收藏
页码:654 / 659
页数:6
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