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HSDL2 Promotes Bladder Cancer Growth In Vitro and In Vivo

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 stu...

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Autores principales: Jia, Ling-Hua, Hu, Mei-Di, Liu, Yuan, Xiong, Xing, Wang, Wei-Jia, Wang, Jin-Gen, Li, Qiu-Gen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566746/
https://www.ncbi.nlm.nih.gov/pubmed/31217732
http://dx.doi.org/10.7150/ijms.31288
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author Jia, Ling-Hua
Hu, Mei-Di
Liu, Yuan
Xiong, Xing
Wang, Wei-Jia
Wang, Jin-Gen
Li, Qiu-Gen
author_facet Jia, Ling-Hua
Hu, Mei-Di
Liu, Yuan
Xiong, Xing
Wang, Wei-Jia
Wang, Jin-Gen
Li, Qiu-Gen
author_sort Jia, Ling-Hua
collection PubMed
description 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.
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spelling pubmed-65667462019-06-19 HSDL2 Promotes Bladder Cancer Growth In Vitro and In Vivo Jia, Ling-Hua Hu, Mei-Di Liu, Yuan Xiong, Xing Wang, Wei-Jia Wang, Jin-Gen Li, Qiu-Gen Int J Med Sci Research Paper 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. Ivyspring International Publisher 2019-05-07 /pmc/articles/PMC6566746/ /pubmed/31217732 http://dx.doi.org/10.7150/ijms.31288 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Jia, Ling-Hua
Hu, Mei-Di
Liu, Yuan
Xiong, Xing
Wang, Wei-Jia
Wang, Jin-Gen
Li, Qiu-Gen
HSDL2 Promotes Bladder Cancer Growth In Vitro and In Vivo
title HSDL2 Promotes Bladder Cancer Growth In Vitro and In Vivo
title_full HSDL2 Promotes Bladder Cancer Growth In Vitro and In Vivo
title_fullStr HSDL2 Promotes Bladder Cancer Growth In Vitro and In Vivo
title_full_unstemmed HSDL2 Promotes Bladder Cancer Growth In Vitro and In Vivo
title_short HSDL2 Promotes Bladder Cancer Growth In Vitro and In Vivo
title_sort hsdl2 promotes bladder cancer growth in vitro and in vivo
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566746/
https://www.ncbi.nlm.nih.gov/pubmed/31217732
http://dx.doi.org/10.7150/ijms.31288
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