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Overexpression of LAPTM4B-35: A Novel Marker of Poor Prognosis of Prostate Cancer

BACKGROUND: Lysosome-associated protein transmembrane 4b-35 (LAPTM4B-35) is a member of the mammalian 4-tetratransmembrane spanning protein superfamily, which is overexpressed in several solid malignancies. However, the expression of LAPTM4B-35 and its role in the progression of prostate cancer (PCa...

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Autores principales: Zhang, Hongtuan, Wei, Qiang, Liu, Ranlu, Qi, Shiyong, Liang, Peihe, Qi, Can, Wang, Andi, Sheng, Bin, Li, Liang, Xu, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961215/
https://www.ncbi.nlm.nih.gov/pubmed/24651764
http://dx.doi.org/10.1371/journal.pone.0091069
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author Zhang, Hongtuan
Wei, Qiang
Liu, Ranlu
Qi, Shiyong
Liang, Peihe
Qi, Can
Wang, Andi
Sheng, Bin
Li, Liang
Xu, Yong
author_facet Zhang, Hongtuan
Wei, Qiang
Liu, Ranlu
Qi, Shiyong
Liang, Peihe
Qi, Can
Wang, Andi
Sheng, Bin
Li, Liang
Xu, Yong
author_sort Zhang, Hongtuan
collection PubMed
description BACKGROUND: Lysosome-associated protein transmembrane 4b-35 (LAPTM4B-35) is a member of the mammalian 4-tetratransmembrane spanning protein superfamily, which is overexpressed in several solid malignancies. However, the expression of LAPTM4B-35 and its role in the progression of prostate cancer (PCa) is unknown. The aim of the present study was to investigate the LAPTM4B-35 expression in PCa and its potential relevance to clinicopathological variables and prognosis. METHODS: Immunohistochemistry was used to determine the expression of LAPTM4B-35 protein in 180 PCa tissues in comparison with 180 normal benign prostatic hyperplasia (BPH) specimens. The correlation between the expression of the LAPTM4B-35 protein and the clinicopathologic characteristics of patients with PCa was analyzed. RESULTS: Statistical analysis showed that LAPTM4B-35 expression was significantly elevated in PCa compared with the BPH controls. High LAPTM4B-35 staining was present in 71.11% of all the cases with PCa. The overexpression of LAPTM4B-35 was significantly associated with the lymph node metastasis, seminal vesicle invasion, PCa stage, higher Gleason score, higher preoperative PSA, and biochemical recurrence (BCR). The Kaplan-Meier survival analysis showed that the high expression of LAPTM4B-35 was related to the poor overall survival and BCR-free survival of patients with PCa. Multivariate Cox analysis showed that LAPTM4B-35 was an independent prognostic factor for both overall survival and BCR-free survival of patients with PCa. CONCLUSIONS: Overexpression of LAPTM4B-35 may be associated with tumor progression and poor prognosis in PCa and thus may serve as a new molecular marker to predict the prognosis of PCa patients.
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spelling pubmed-39612152014-03-24 Overexpression of LAPTM4B-35: A Novel Marker of Poor Prognosis of Prostate Cancer Zhang, Hongtuan Wei, Qiang Liu, Ranlu Qi, Shiyong Liang, Peihe Qi, Can Wang, Andi Sheng, Bin Li, Liang Xu, Yong PLoS One Research Article BACKGROUND: Lysosome-associated protein transmembrane 4b-35 (LAPTM4B-35) is a member of the mammalian 4-tetratransmembrane spanning protein superfamily, which is overexpressed in several solid malignancies. However, the expression of LAPTM4B-35 and its role in the progression of prostate cancer (PCa) is unknown. The aim of the present study was to investigate the LAPTM4B-35 expression in PCa and its potential relevance to clinicopathological variables and prognosis. METHODS: Immunohistochemistry was used to determine the expression of LAPTM4B-35 protein in 180 PCa tissues in comparison with 180 normal benign prostatic hyperplasia (BPH) specimens. The correlation between the expression of the LAPTM4B-35 protein and the clinicopathologic characteristics of patients with PCa was analyzed. RESULTS: Statistical analysis showed that LAPTM4B-35 expression was significantly elevated in PCa compared with the BPH controls. High LAPTM4B-35 staining was present in 71.11% of all the cases with PCa. The overexpression of LAPTM4B-35 was significantly associated with the lymph node metastasis, seminal vesicle invasion, PCa stage, higher Gleason score, higher preoperative PSA, and biochemical recurrence (BCR). The Kaplan-Meier survival analysis showed that the high expression of LAPTM4B-35 was related to the poor overall survival and BCR-free survival of patients with PCa. Multivariate Cox analysis showed that LAPTM4B-35 was an independent prognostic factor for both overall survival and BCR-free survival of patients with PCa. CONCLUSIONS: Overexpression of LAPTM4B-35 may be associated with tumor progression and poor prognosis in PCa and thus may serve as a new molecular marker to predict the prognosis of PCa patients. Public Library of Science 2014-03-20 /pmc/articles/PMC3961215/ /pubmed/24651764 http://dx.doi.org/10.1371/journal.pone.0091069 Text en © 2014 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Hongtuan
Wei, Qiang
Liu, Ranlu
Qi, Shiyong
Liang, Peihe
Qi, Can
Wang, Andi
Sheng, Bin
Li, Liang
Xu, Yong
Overexpression of LAPTM4B-35: A Novel Marker of Poor Prognosis of Prostate Cancer
title Overexpression of LAPTM4B-35: A Novel Marker of Poor Prognosis of Prostate Cancer
title_full Overexpression of LAPTM4B-35: A Novel Marker of Poor Prognosis of Prostate Cancer
title_fullStr Overexpression of LAPTM4B-35: A Novel Marker of Poor Prognosis of Prostate Cancer
title_full_unstemmed Overexpression of LAPTM4B-35: A Novel Marker of Poor Prognosis of Prostate Cancer
title_short Overexpression of LAPTM4B-35: A Novel Marker of Poor Prognosis of Prostate Cancer
title_sort overexpression of laptm4b-35: a novel marker of poor prognosis of prostate cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961215/
https://www.ncbi.nlm.nih.gov/pubmed/24651764
http://dx.doi.org/10.1371/journal.pone.0091069
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