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CC chemokine ligand 18 correlates with malignant progression of prostate cancer.
Chen, Guo; Liang, Yu-xiang; Zhu, Jian-guo; Fu, Xin; Chen, Yan-fei; Mo, Ru-jun; Zhou, Liang; Fu, Hao; Bi, Xue-cheng; He, Hui-chan; Yang, Sheng-bang; Wu, Yong-ding; Jiang, Fu-neng; Zhong, Wei-de.
Affiliation
  • Chen G; Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, China.
  • Liang YX; Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, China.
  • Zhu JG; Department of Urology, Guizhou Provincial People's Hospital, Guizhou 550002, China.
  • Fu X; Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, China.
  • Chen YF; Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, China.
  • Mo RJ; Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, China.
  • Zhou L; Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, China.
  • Fu H; Department of Urology, Nanhua Hospital Affiliated Nanhua University, Hengyang, Hunan 421002, China.
  • Bi XC; Department of Urology, Guangdong General Hospital, Guangzhou 510080, China.
  • He HC; Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, China.
  • Yang SB; Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, China.
  • Wu YD; Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, China.
  • Jiang FN; Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, China.
  • Zhong WD; Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, China ; Guangdong Provincial Institute of Nephrology, Southern Medical University, Guangzhou 510515, China.
Biomed Res Int ; 2014: 230183, 2014.
Article in En | MEDLINE | ID: mdl-25197632
ABSTRACT
BACKGROUND AND

AIM:

CC chemokine ligand 18 (CCL18) promotes malignant behaviors of various human cancer types. However, its involvement in human prostate cancer has not been fully elucidated. The aim of this study was to investigate the role of CCL18 in PCa.

METHODS:

Expression of CCL18 at mRNA and protein levels was detected using real-time qRT-PCR and immunohistochemistry analysis. We analyzed the associations of CCL18 expression with clinical features of human PCa. The effects of PCa cell migration, invasion, and apoptosis were tested. The efficiency of CCL18 on prostate tumor growth was assessed in a subcutaneous xenograft model.

RESULTS:

CCL18 expression was upregulated (both P < 0.01) in PCa tissues compared with those in noncancerous prostate tissues. CCL18 upregulation was correlated with high Gleason score (P = 0.034) of patients with PCa. rCCL18 stimulation in PCa cells promoted cell migration and invasion but decreased DU145 cells apoptosis rate. Furthermore, subcutaneous homografts models showed the increased tumor growth and tumor vascularization with the CCL18 stimulation, and the expression of Ki67, PCNA, and CD31 in CCL18 stimulation mice was also significantly increased.

CONCLUSIONS:

Our data offer the convincing evidence that the upregulation of CCL18 may be involved in the malignant progression of PCa.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Disease Progression / Chemokines, CC Type of study: Prognostic_studies Limits: Aged / Animals / Humans / Male / Middle aged Language: En Journal: Biomed Res Int Year: 2014 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Disease Progression / Chemokines, CC Type of study: Prognostic_studies Limits: Aged / Animals / Humans / Male / Middle aged Language: En Journal: Biomed Res Int Year: 2014 Document type: Article Affiliation country: China