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

• Published in: Oncology letters Vol. 22; no. 5; p. 1
• Main Authors: Yin, Yanhua, Fan, Yanyan, Yu, Gang, Du, Ying
• Format: Journal Article
• Language: English
• Published: Athens Spandidos Publications 01-11-2021; Spandidos Publications UK Ltd; D.A. Spandidos
• Subjects: Antibodies; Autophagy; Bladder cancer; Cancer; Care and treatment; Cell growth; Gastric cancer; Immunohistochemistry; Medical prognosis; Metastasis; Oncology; Plasmids; Proteins; Scientific equipment and supplies industry; Survival analysis; United States; China
• ISSN: 1792-1074; 1792-1082
• DOI: 10.3892/ol.2021.13026

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 4[beta] (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.