Up‐regulation of LIMK1 expression in prostate cancer is correlated with poor pathological features, lymph node metastases and biochemical recurrence
This study aimed to explore the association between LIM domain kinase 1 (LIMK1) expression in prostate cancer (PCa) tissues with advanced pathological features, lymph node metastases and biochemical recurrence. A total of 279 PCa specimens from patients who underwent radical prostatectomy and 50 ben...
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Published in | Journal of cellular and molecular medicine Vol. 24; no. 8; pp. 4698 - 4706 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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England
John Wiley & Sons, Inc
01.04.2020
John Wiley and Sons Inc |
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Abstract | This study aimed to explore the association between LIM domain kinase 1 (LIMK1) expression in prostate cancer (PCa) tissues with advanced pathological features, lymph node metastases and biochemical recurrence. A total of 279 PCa specimens from patients who underwent radical prostatectomy and 50 benign prostatic hyperplasia (BPH) specimens were collected to construct tissue microarray, which were subjected to immunohistochemical staining for LIMK1 expression subsequently. Logistic and Cox regression analysis were used to evaluate the relationship between LIMK1 expression and clinicopathological features of patients with PCa. Immunohistochemical staining assay demonstrated that LIMK1 expression was significantly higher in PCa than BPH specimens (77.1% vs 26.0%; P < .001). LIMK1 expression was significantly higher in positive lymph node specimens than corresponding PCa specimens (P = .002; P < .001). Up‐regulation of LIMK1 was associated with prostate volume, prostate‐specific antigen, prostate‐specific antigen density, Gleason score, T stage, lymph node metastases, extracapsular extension and seminal vesicle invasion, and positive surgical margin. Multivariate logistic regression analysis demonstrated that LIMK1 was an independent risk factor for PCa lymph node metastasis (P < .05). Multivariate Cox regression analysis revealed that the up‐regulation of LIMK1 was an independent risk factor for biochemical recurrence. Kaplan‐Meier analysis indicated that up‐regulation LIMK1 was associated with shortened biochemical‐free survival (BFS) after radical prostatectomy (P < .001). In conclusion, LIMK1 was significantly up‐regulated in PCa and positive lymph node specimens and correlated with lymph node metastasis and shortened BFS of PCa. The underlying molecular mechanism of LIMK1 in PCa should be further evaluated. |
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AbstractList | This study aimed to explore the association between LIM domain kinase 1 (LIMK1) expression in prostate cancer (PCa) tissues with advanced pathological features, lymph node metastases and biochemical recurrence. A total of 279 PCa specimens from patients who underwent radical prostatectomy and 50 benign prostatic hyperplasia (BPH) specimens were collected to construct tissue microarray, which were subjected to immunohistochemical staining for LIMK1 expression subsequently. Logistic and Cox regression analysis were used to evaluate the relationship between LIMK1 expression and clinicopathological features of patients with PCa. Immunohistochemical staining assay demonstrated that LIMK1 expression was significantly higher in PCa than BPH specimens (77.1% vs 26.0%; P < .001). LIMK1 expression was significantly higher in positive lymph node specimens than corresponding PCa specimens (P = .002; P < .001). Up-regulation of LIMK1 was associated with prostate volume, prostate-specific antigen, prostate-specific antigen density, Gleason score, T stage, lymph node metastases, extracapsular extension and seminal vesicle invasion, and positive surgical margin. Multivariate logistic regression analysis demonstrated that LIMK1 was an independent risk factor for PCa lymph node metastasis (P < .05). Multivariate Cox regression analysis revealed that the up-regulation of LIMK1 was an independent risk factor for biochemical recurrence. Kaplan-Meier analysis indicated that up-regulation LIMK1 was associated with shortened biochemical-free survival (BFS) after radical prostatectomy (P < .001). In conclusion, LIMK1 was significantly up-regulated in PCa and positive lymph node specimens and correlated with lymph node metastasis and shortened BFS of PCa. The underlying molecular mechanism of LIMK1 in PCa should be further evaluated. This study aimed to explore the association between LIM domain kinase 1 (LIMK1) expression in prostate cancer (PCa) tissues with advanced pathological features, lymph node metastases and biochemical recurrence. A total of 279 PCa specimens from patients who underwent radical prostatectomy and 50 benign prostatic hyperplasia (BPH) specimens were collected to construct tissue microarray, which were subjected to immunohistochemical staining for LIMK1 expression subsequently. Logistic and Cox regression analysis were used to evaluate the relationship between LIMK1 expression and clinicopathological features of patients with PCa. Immunohistochemical staining assay demonstrated that LIMK1 expression was significantly higher in PCa than BPH specimens (77.1% vs 26.0%; P < .001). LIMK1 expression was significantly higher in positive lymph node specimens than corresponding PCa specimens ( P = .002; P < .001). Up‐regulation of LIMK1 was associated with prostate volume, prostate‐specific antigen, prostate‐specific antigen density, Gleason score, T stage, lymph node metastases, extracapsular extension and seminal vesicle invasion, and positive surgical margin. Multivariate logistic regression analysis demonstrated that LIMK1 was an independent risk factor for PCa lymph node metastasis ( P < .05). Multivariate Cox regression analysis revealed that the up‐regulation of LIMK1 was an independent risk factor for biochemical recurrence. Kaplan‐Meier analysis indicated that up‐regulation LIMK1 was associated with shortened biochemical‐free survival (BFS) after radical prostatectomy ( P < .001). In conclusion, LIMK1 was significantly up‐regulated in PCa and positive lymph node specimens and correlated with lymph node metastasis and shortened BFS of PCa. The underlying molecular mechanism of LIMK1 in PCa should be further evaluated. This study aimed to explore the association between LIM domain kinase 1 (LIMK1) expression in prostate cancer (PCa) tissues with advanced pathological features, lymph node metastases and biochemical recurrence. A total of 279 PCa specimens from patients who underwent radical prostatectomy and 50 benign prostatic hyperplasia (BPH) specimens were collected to construct tissue microarray, which were subjected to immunohistochemical staining for LIMK1 expression subsequently. Logistic and Cox regression analysis were used to evaluate the relationship between LIMK1 expression and clinicopathological features of patients with PCa. Immunohistochemical staining assay demonstrated that LIMK1 expression was significantly higher in PCa than BPH specimens (77.1% vs 26.0%; P < .001). LIMK1 expression was significantly higher in positive lymph node specimens than corresponding PCa specimens (P = .002; P < .001). Up‐regulation of LIMK1 was associated with prostate volume, prostate‐specific antigen, prostate‐specific antigen density, Gleason score, T stage, lymph node metastases, extracapsular extension and seminal vesicle invasion, and positive surgical margin. Multivariate logistic regression analysis demonstrated that LIMK1 was an independent risk factor for PCa lymph node metastasis (P < .05). Multivariate Cox regression analysis revealed that the up‐regulation of LIMK1 was an independent risk factor for biochemical recurrence. Kaplan‐Meier analysis indicated that up‐regulation LIMK1 was associated with shortened biochemical‐free survival (BFS) after radical prostatectomy (P < .001). In conclusion, LIMK1 was significantly up‐regulated in PCa and positive lymph node specimens and correlated with lymph node metastasis and shortened BFS of PCa. The underlying molecular mechanism of LIMK1 in PCa should be further evaluated. This study aimed to explore the association between LIM domain kinase 1 (LIMK1) expression in prostate cancer (PCa) tissues with advanced pathological features, lymph node metastases and biochemical recurrence. A total of 279 PCa specimens from patients who underwent radical prostatectomy and 50 benign prostatic hyperplasia (BPH) specimens were collected to construct tissue microarray, which were subjected to immunohistochemical staining for LIMK1 expression subsequently. Logistic and Cox regression analysis were used to evaluate the relationship between LIMK1 expression and clinicopathological features of patients with PCa. Immunohistochemical staining assay demonstrated that LIMK1 expression was significantly higher in PCa than BPH specimens (77.1% vs 26.0%; P < .001). LIMK1 expression was significantly higher in positive lymph node specimens than corresponding PCa specimens (P = .002; P < .001). Up-regulation of LIMK1 was associated with prostate volume, prostate-specific antigen, prostate-specific antigen density, Gleason score, T stage, lymph node metastases, extracapsular extension and seminal vesicle invasion, and positive surgical margin. Multivariate logistic regression analysis demonstrated that LIMK1 was an independent risk factor for PCa lymph node metastasis (P < .05). Multivariate Cox regression analysis revealed that the up-regulation of LIMK1 was an independent risk factor for biochemical recurrence. Kaplan-Meier analysis indicated that up-regulation LIMK1 was associated with shortened biochemical-free survival (BFS) after radical prostatectomy (P < .001). In conclusion, LIMK1 was significantly up-regulated in PCa and positive lymph node specimens and correlated with lymph node metastasis and shortened BFS of PCa. The underlying molecular mechanism of LIMK1 in PCa should be further evaluated.This study aimed to explore the association between LIM domain kinase 1 (LIMK1) expression in prostate cancer (PCa) tissues with advanced pathological features, lymph node metastases and biochemical recurrence. A total of 279 PCa specimens from patients who underwent radical prostatectomy and 50 benign prostatic hyperplasia (BPH) specimens were collected to construct tissue microarray, which were subjected to immunohistochemical staining for LIMK1 expression subsequently. Logistic and Cox regression analysis were used to evaluate the relationship between LIMK1 expression and clinicopathological features of patients with PCa. Immunohistochemical staining assay demonstrated that LIMK1 expression was significantly higher in PCa than BPH specimens (77.1% vs 26.0%; P < .001). LIMK1 expression was significantly higher in positive lymph node specimens than corresponding PCa specimens (P = .002; P < .001). Up-regulation of LIMK1 was associated with prostate volume, prostate-specific antigen, prostate-specific antigen density, Gleason score, T stage, lymph node metastases, extracapsular extension and seminal vesicle invasion, and positive surgical margin. Multivariate logistic regression analysis demonstrated that LIMK1 was an independent risk factor for PCa lymph node metastasis (P < .05). Multivariate Cox regression analysis revealed that the up-regulation of LIMK1 was an independent risk factor for biochemical recurrence. Kaplan-Meier analysis indicated that up-regulation LIMK1 was associated with shortened biochemical-free survival (BFS) after radical prostatectomy (P < .001). In conclusion, LIMK1 was significantly up-regulated in PCa and positive lymph node specimens and correlated with lymph node metastasis and shortened BFS of PCa. The underlying molecular mechanism of LIMK1 in PCa should be further evaluated. |
Author | Cai, Hai Chen, Shao‐Hao Wei, Yong Xu, Ning Wu, Yu‐Peng Huang, Jin‐Bei Lin, Yun‐Zhi Li, Xiao‐Dong Sun, Xiong‐Lin Zheng, Qing‐Shui Xue, Xue‐Yi |
AuthorAffiliation | 1 Departments of Urology The First Affiliated Hospital of Fujian Medical University Fuzhou China |
AuthorAffiliation_xml | – name: 1 Departments of Urology The First Affiliated Hospital of Fujian Medical University Fuzhou China |
Author_xml | – sequence: 1 givenname: Jin‐Bei surname: Huang fullname: Huang, Jin‐Bei organization: The First Affiliated Hospital of Fujian Medical University – sequence: 2 givenname: Yu‐Peng surname: Wu fullname: Wu, Yu‐Peng organization: The First Affiliated Hospital of Fujian Medical University – sequence: 3 givenname: Yun‐Zhi surname: Lin fullname: Lin, Yun‐Zhi organization: The First Affiliated Hospital of Fujian Medical University – sequence: 4 givenname: Hai surname: Cai fullname: Cai, Hai organization: The First Affiliated Hospital of Fujian Medical University – sequence: 5 givenname: Shao‐Hao surname: Chen fullname: Chen, Shao‐Hao organization: The First Affiliated Hospital of Fujian Medical University – sequence: 6 givenname: Xiong‐Lin surname: Sun fullname: Sun, Xiong‐Lin organization: The First Affiliated Hospital of Fujian Medical University – sequence: 7 givenname: Xiao‐Dong surname: Li fullname: Li, Xiao‐Dong organization: The First Affiliated Hospital of Fujian Medical University – sequence: 8 givenname: Yong surname: Wei fullname: Wei, Yong organization: The First Affiliated Hospital of Fujian Medical University – sequence: 9 givenname: Qing‐Shui orcidid: 0000-0002-7426-6501 surname: Zheng fullname: Zheng, Qing‐Shui organization: The First Affiliated Hospital of Fujian Medical University – sequence: 10 givenname: Ning surname: Xu fullname: Xu, Ning email: drxun@fjmu.edu.cn organization: The First Affiliated Hospital of Fujian Medical University – sequence: 11 givenname: Xue‐Yi orcidid: 0000-0002-6461-7435 surname: Xue fullname: Xue, Xue‐Yi email: xuexueyi@fjmu.edu.cn organization: The First Affiliated Hospital of Fujian Medical University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32168432$$D View this record in MEDLINE/PubMed |
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Copyright | 2020 The Authors. published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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DOI | 10.1111/jcmm.15138 |
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Keywords | LIM domain kinase 1 prostate cancer advanced pathological features biochemical recurrence lymph node metastasis |
Language | English |
License | Attribution 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
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Notes | Funding information This study was supported by Foundation of Fujian Provincial Department Of Finance (Grant Number: 2018B011), Startup Fund for scientific research, Fujian Medical University (Grant Numbers: 2017XQ2041, 2016QH050 and 2018QH1065), the Youth Foundation of Health and Family Planning Commission of Fujian Province, China (Grant Numbers: 2018‐1‐51 and 2018‐1‐50), the Joint Foundation of Fujian Province for Science and Technology Innovative Research Project (Grant Number: 2017Y9093), and Natural Science Foundation of Fujian Province (Grant Number: 2017J01197). ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Huang, Wu, Lin, and Cai contributed equally to this work. |
ORCID | 0000-0002-7426-6501 0000-0002-6461-7435 |
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SubjectTerms | advanced pathological features Aged Androgens Antigens biochemical recurrence Cancer surgery Cancer therapies Cell cycle Disease-Free Survival Endocrine therapy Gene Expression Regulation, Neoplastic - genetics Humans Hyperplasia Kaplan-Meier Estimate LIM domain kinase 1 LIM kinase Lim Kinases - genetics lymph node metastasis Lymph nodes Lymph Nodes - metabolism Lymph Nodes - pathology Lymphatic Metastasis - genetics Lymphatic Metastasis - pathology Lymphatic system Male Medical prognosis Medical research Metastases Metastasis Middle Aged Neoplasm Recurrence, Local - genetics Neoplasm Recurrence, Local - pathology Original Prostate - metabolism Prostate - pathology Prostate cancer Prostatectomy Prostatic Neoplasms - genetics Prostatic Neoplasms - pathology Radiation therapy Regression analysis Risk factors Seminal vesicle Survival Analysis Tumors Up-regulation |
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Title | Up‐regulation of LIMK1 expression in prostate cancer is correlated with poor pathological features, lymph node metastases and biochemical recurrence |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjcmm.15138 https://www.ncbi.nlm.nih.gov/pubmed/32168432 https://www.proquest.com/docview/2393252839 https://www.proquest.com/docview/2377333247 https://pubmed.ncbi.nlm.nih.gov/PMC7176864 |
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