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LAPTM4B promotes the progression of bladder cancer by stimulating cell proliferation and invasion

Bladder cancer is a highly metastatic tumor and one of the most common malignant tumors originating in the urinary system. Due to the complicated etiology and lack of significant early symptoms, the diagnosis and treatment of bladder cancer is difficult. Lysosome-associated transmembrane protein 4β...

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Autores principales: Yin, Yanhua, Fan, Yanyan, Yu, Gang, Du, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8442228/
https://www.ncbi.nlm.nih.gov/pubmed/34589144
http://dx.doi.org/10.3892/ol.2021.13026
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author Yin, Yanhua
Fan, Yanyan
Yu, Gang
Du, Ying
author_facet Yin, Yanhua
Fan, Yanyan
Yu, Gang
Du, Ying
author_sort Yin, Yanhua
collection PubMed
description Bladder cancer is a highly metastatic tumor and one of the most common malignant tumors originating in the urinary system. Due to the complicated etiology and lack of significant early symptoms, the diagnosis and treatment of bladder cancer is difficult. Lysosome-associated transmembrane protein 4β (LAPTM4B) was reported to be involved in the development and progression of several types of tumor, however, its potential effect on the development and metastasis of bladder cancer is still unclear. Immunohistochemistry was performed to detect the protein expression level of LAPTM4B in bladder cancer tissues and short hairpin RNAs targeting LAPTM4B were transfected into bladder cancer cells to knockdown its expression. MTT and colony formation assays were performed to detect cell proliferation, while wound healing and Transwell invasion assays were performed to detect cell migration and invasion, respectively. In addition, tumor growth assays were performed to confirm the effects of LAPTM4B in mice. The present study demonstrated that LAPTM4B was associated with the prognosis of patients with bladder cancer. In addition, LAPTM4B was associated with clinical characteristics, including tumor stage and recurrence. The results further showed that LAPTM4B knockdown could suppress the proliferation of bladder cancer cell lines. In addition, the migration and invasion of T24 and 5637 cells was suppressed following LAPTM4B knockdown in vitro. The in vivo data confirmed that knockdown of LAPTM4B markedly inhibited tumor growth and metastasis in mice. In summary, the results from the present study provide strong evidence of the effects of LAPTM4B in bladder cancer progression.
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spelling pubmed-84422282021-09-28 LAPTM4B promotes the progression of bladder cancer by stimulating cell proliferation and invasion Yin, Yanhua Fan, Yanyan Yu, Gang Du, Ying Oncol Lett Articles Bladder cancer is a highly metastatic tumor and one of the most common malignant tumors originating in the urinary system. Due to the complicated etiology and lack of significant early symptoms, the diagnosis and treatment of bladder cancer is difficult. Lysosome-associated transmembrane protein 4β (LAPTM4B) was reported to be involved in the development and progression of several types of tumor, however, its potential effect on the development and metastasis of bladder cancer is still unclear. Immunohistochemistry was performed to detect the protein expression level of LAPTM4B in bladder cancer tissues and short hairpin RNAs targeting LAPTM4B were transfected into bladder cancer cells to knockdown its expression. MTT and colony formation assays were performed to detect cell proliferation, while wound healing and Transwell invasion assays were performed to detect cell migration and invasion, respectively. In addition, tumor growth assays were performed to confirm the effects of LAPTM4B in mice. The present study demonstrated that LAPTM4B was associated with the prognosis of patients with bladder cancer. In addition, LAPTM4B was associated with clinical characteristics, including tumor stage and recurrence. The results further showed that LAPTM4B knockdown could suppress the proliferation of bladder cancer cell lines. In addition, the migration and invasion of T24 and 5637 cells was suppressed following LAPTM4B knockdown in vitro. The in vivo data confirmed that knockdown of LAPTM4B markedly inhibited tumor growth and metastasis in mice. In summary, the results from the present study provide strong evidence of the effects of LAPTM4B in bladder cancer progression. D.A. Spandidos 2021-11 2021-09-08 /pmc/articles/PMC8442228/ /pubmed/34589144 http://dx.doi.org/10.3892/ol.2021.13026 Text en Copyright: © Yin et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Yin, Yanhua
Fan, Yanyan
Yu, Gang
Du, Ying
LAPTM4B promotes the progression of bladder cancer by stimulating cell proliferation and invasion
title LAPTM4B promotes the progression of bladder cancer by stimulating cell proliferation and invasion
title_full LAPTM4B promotes the progression of bladder cancer by stimulating cell proliferation and invasion
title_fullStr LAPTM4B promotes the progression of bladder cancer by stimulating cell proliferation and invasion
title_full_unstemmed LAPTM4B promotes the progression of bladder cancer by stimulating cell proliferation and invasion
title_short LAPTM4B promotes the progression of bladder cancer by stimulating cell proliferation and invasion
title_sort laptm4b promotes the progression of bladder cancer by stimulating cell proliferation and invasion
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8442228/
https://www.ncbi.nlm.nih.gov/pubmed/34589144
http://dx.doi.org/10.3892/ol.2021.13026
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