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Elevated YKL40 is associated with advanced prostate cancer (PCa) and positively regulates invasion and migration of PCa cells
被引:28
作者:
Jeet, Varinder
[1
]
Tevz, Gregor
[1
]
Lehman, Melanie
[1
,2
]
Hollier, Brett
[1
]
Nelson, Colleen
[1
,2
]
机构:
[1] Queensland Univ Technol, Princess Alexandra Hosp, Australian Prostate Canc Res Ctr Queensland, Inst Hlth & Biomed Innovat,Translat Res Inst, Brisbane, Qld 4001, Australia
[2] Univ British Columbia, Vancouver Prostate Ctr, Dept Urol Sci, Vancouver, BC V5Z 1M9, Canada
关键词:
YKL40;
prostate cancer;
cell migration;
cell invasion;
metastasis;
targeted therapy;
SERUM YKL-40 LEVELS;
ANDROGEN RECEPTOR;
SECRETED GLYCOPROTEIN;
BREAST-CANCER;
PATHWAY;
PROGRESSION;
PROTEIN;
EXPRESSION;
BIOMARKER;
METASTASIS;
D O I:
10.1530/ERC-14-0267
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Chitinase 3-like 1 (CHI3L1 or YKL40) is a secreted glycoprotein highly expressed in tumours from patients with advanced stage cancers, including prostate cancer (PCa). The exact function of YKL40 is poorly understood, but it has been shown to play an important role in promoting tumour angiogenesis and metastasis. The therapeutic value and biological function of YKL40 are unknown in PCa. The objective of this study was to examine the expression and function of YKL40 in PCa. Gene expression analysis demonstrated that YKL40 was highly expressed in metastatic PCa cells when compared with less invasive and normal prostate epithelial cell lines. In addition, the expression was primarily limited to androgen receptor-positive cell lines. Evaluation of YKL40 tissue expression in PCa patients showed a progressive increase in patients with aggressive disease when compared with those with less aggressive cancers and normal controls. Treatment of LNCaP and C4-2B cells with androgens increased YKL40 expression, whereas treatment with an anti-androgen agent decreased the gene expression of YKL40 in androgen-sensitive LNCaP cells. Furthermore, knockdown of YKL40 significantly decreased invasion and migration of PCa cells, whereas overexpression rendered them more invasive and migratory, which was commensurate with an enhancement in the anchorage-independent growth of cells. To our knowledge, this study characterises the role of YKL40 for the first time in PCa. Together, these results suggest that YKL40 plays an important role in PCa progression and thus inhibition of YKL40 may be a potential therapeutic strategy for the treatment of PCa.
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页码:723 / 737
页数:15
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