The HtrA1 serine protease is down-regulated during human melanoma progression and represses growth of metastatic melanoma cells

被引:165
作者
Baldi, A
De Luca, A
Morini, M
Battista, T
Felsani, A
Baldi, F
Catricalà, C
Amantea, A
Noonan, DM
Albini, A
Natali, PG
Lombardi, D
Paggi, MG
机构
[1] Regina Elena Inst Canc Res, Ctr Expt Res, Dept Dev Therapeut Programs, Lab C,CRS, I-00158 Rome, Italy
[2] Natl Inst Canc Res, Genoa, Italy
[3] CNR, Ist Neurobiol & Med Mol, Rome, Italy
[4] Univ Naples 2, Sect Pathol, Dept Biochem & Biophys F Cedrangolo, Naples, Italy
[5] San Gallicano Dermatol Inst, Rome, Italy
[6] Regina Elena Inst Canc Res, CRS, Immunol Lab, Rome, Italy
[7] Univ Aquila, Dept Expt Med, I-67100 Laquila, Italy
关键词
melanoma; tumor progression; PRSS11; HtrA1; serine protease;
D O I
10.1038/sj.onc.1205911
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Differential gene expression of cell lines derived from a malignant melanoma or its autologous lymph node metastasis using cDNA arrays indicated down-regulation of PRSS11, a gene encoding the serine protease HtrA1, a homolog of the Escherichia coli protease HtrA, in the metastatic line. Stable PRSS11 overexpression in the metastatic cell line strongly inhibited proliferation, chemoinvasion and Nm23-H1 protein expression in vitro, as well as cell growth in vivo in nu/nu mice. A polyclonal anti-HtrA1 serum demonstrated a significantly higher expression in primary melanomas when compared to unrelated metastatic lesions in a human melanoma tissue array, and down-modulation of HtrA1 expression in autologous lymph node melanoma metastases in seven out of 11 cases examined. These results suggest that down-regulation of PRSS11 and HtrA1 expression may represent an indicator of melanoma progression.
引用
收藏
页码:6684 / 6688
页数:5
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