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Overexpression of LARP1 predicts poor prognosis of colorectal cancer and is expected to be a potential therapeutic target
This study investigated the significance of La-related protein 1 (LARP1) in the development and progression of colorectal cancer (CRC). Quantitative real-time polymerase chain reaction and Western blot analyses were carried out to determine the mRNA and protein expression of LARP1 in CRC tumor tissu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126195/ https://www.ncbi.nlm.nih.gov/pubmed/27614686 http://dx.doi.org/10.1007/s13277-016-5332-3 |
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author | Ye, Ling Lin, Sheng-tao Mi, Yu-shuai Liu, Yuan Ma, Yang Sun, Hui-min Peng, Zhi-hai Fan, Jun-wei |
author_facet | Ye, Ling Lin, Sheng-tao Mi, Yu-shuai Liu, Yuan Ma, Yang Sun, Hui-min Peng, Zhi-hai Fan, Jun-wei |
author_sort | Ye, Ling |
collection | PubMed |
description | This study investigated the significance of La-related protein 1 (LARP1) in the development and progression of colorectal cancer (CRC). Quantitative real-time polymerase chain reaction and Western blot analyses were carried out to determine the mRNA and protein expression of LARP1 in CRC tumor tissues and paired adjacent normal mucosa. The expression of LARP1 was upregulated in CRC. Immunohistochemical analysis using tissue microarray was performed. A positive correlation between LARP1 and proliferating cell nuclear antigen (PCNA) in the area of proliferation was observed using the Spearman’s correlation coefficient test (r = 0.332, P < 0.01). The elevated expression of LARP1 significantly correlated with T stage (P = 0.02), N stage (P = 0.006), M stage (P < 0.001), American Joint Committee on Cancer (AJCC) stage (P = 0.04), differentiation rank (P < 0.001), and PCNA level (P < 0.001). In addition, the inhibitory effect of LARP1 knockdown on CRC cell proliferation was demonstrated using Cell Counting Kit-8 (CCK8) and colony-forming cell (CFC) assays. Multivariate analysis showed that LARP1 was an independent prognostic factor for overall survival (OS; hazard rate (HR) = 0.244; 95 % confidence interval (CI), 0.078–0.769; P = 0.016) and disease-free survival (DFS; HR = 0.281; 95 % CI, 0.086–0.917; P = 0.035) in CRC patients. LARP1 plays an important role in the proliferation of colorectal cancer and represents a new prognostic indicator. |
format | Online Article Text |
id | pubmed-5126195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-51261952016-12-13 Overexpression of LARP1 predicts poor prognosis of colorectal cancer and is expected to be a potential therapeutic target Ye, Ling Lin, Sheng-tao Mi, Yu-shuai Liu, Yuan Ma, Yang Sun, Hui-min Peng, Zhi-hai Fan, Jun-wei Tumour Biol Original Article This study investigated the significance of La-related protein 1 (LARP1) in the development and progression of colorectal cancer (CRC). Quantitative real-time polymerase chain reaction and Western blot analyses were carried out to determine the mRNA and protein expression of LARP1 in CRC tumor tissues and paired adjacent normal mucosa. The expression of LARP1 was upregulated in CRC. Immunohistochemical analysis using tissue microarray was performed. A positive correlation between LARP1 and proliferating cell nuclear antigen (PCNA) in the area of proliferation was observed using the Spearman’s correlation coefficient test (r = 0.332, P < 0.01). The elevated expression of LARP1 significantly correlated with T stage (P = 0.02), N stage (P = 0.006), M stage (P < 0.001), American Joint Committee on Cancer (AJCC) stage (P = 0.04), differentiation rank (P < 0.001), and PCNA level (P < 0.001). In addition, the inhibitory effect of LARP1 knockdown on CRC cell proliferation was demonstrated using Cell Counting Kit-8 (CCK8) and colony-forming cell (CFC) assays. Multivariate analysis showed that LARP1 was an independent prognostic factor for overall survival (OS; hazard rate (HR) = 0.244; 95 % confidence interval (CI), 0.078–0.769; P = 0.016) and disease-free survival (DFS; HR = 0.281; 95 % CI, 0.086–0.917; P = 0.035) in CRC patients. LARP1 plays an important role in the proliferation of colorectal cancer and represents a new prognostic indicator. Springer Netherlands 2016-09-10 /pmc/articles/PMC5126195/ /pubmed/27614686 http://dx.doi.org/10.1007/s13277-016-5332-3 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Ye, Ling Lin, Sheng-tao Mi, Yu-shuai Liu, Yuan Ma, Yang Sun, Hui-min Peng, Zhi-hai Fan, Jun-wei Overexpression of LARP1 predicts poor prognosis of colorectal cancer and is expected to be a potential therapeutic target |
title | Overexpression of LARP1 predicts poor prognosis of colorectal cancer and is expected to be a potential therapeutic target |
title_full | Overexpression of LARP1 predicts poor prognosis of colorectal cancer and is expected to be a potential therapeutic target |
title_fullStr | Overexpression of LARP1 predicts poor prognosis of colorectal cancer and is expected to be a potential therapeutic target |
title_full_unstemmed | Overexpression of LARP1 predicts poor prognosis of colorectal cancer and is expected to be a potential therapeutic target |
title_short | Overexpression of LARP1 predicts poor prognosis of colorectal cancer and is expected to be a potential therapeutic target |
title_sort | overexpression of larp1 predicts poor prognosis of colorectal cancer and is expected to be a potential therapeutic target |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126195/ https://www.ncbi.nlm.nih.gov/pubmed/27614686 http://dx.doi.org/10.1007/s13277-016-5332-3 |
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