Targeted inhibition of human collagenase-3 (MMP-13) expression inhibits squamous cell carcinoma growth in vivo

被引:66
作者
Ala-aho, R
Ahonen, M
George, SJ
Heikkilä, J
Grènman, R
Kallajoki, M
Kähäri, VM
机构
[1] Univ Turku, Dept Med Biochem & Mol Biol, FIN-20520 Turku, Finland
[2] Univ Turku, Dept Dermatol, FIN-20520 Turku, Finland
[3] Univ Turku, Ctr Biotechnol, SF-20500 Turku, Finland
[4] Bristol Royal Infirm & Gen Hosp, Bristol Heart Inst, Bristol BS2 8HW, Avon, England
[5] Abo Akad Univ, Dept Biochem & Pharm, FIN-20520 Turku, Finland
[6] Univ Turku, Cent Hosp, Dept Otorhinolaryngol Head & Neck Surg, FIN-20520 Turku, Finland
[7] Univ Turku, Cent Hosp, Dept Pathol, FIN-20520 Turku, Finland
关键词
collagenase; squamous cell carcinoma; invasion; ribozyme;
D O I
10.1038/sj.onc.1207678
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
Squamous cell carcinomas (SCCs) of the head and neck are characterized by a high tendency for local invasion and metastasis to lymph nodes. Collagenase-3 (MMP-13) is specifically expressed by tumor cells in SCCs of the head and neck and its expression correlates with their invasion capacity. To specifically examine the role of MMP-13 in the growth and invasion of SCC, we constructed a hammerhead ribozyme targeted against human MMP-13 mRNA. The anti-MMP-13 ribozyme effectively cleaved MMP-13 transcripts in vitro. Adenoviral delivery of the anti-MMP-13 ribozyme to cutaneous metastatic SCC cells in culture resulted in potent and specific inhibition of the production of proMMP-13 and markedly suppressed invasion of SCC cells through Matrigel. In addition, adenoviral delivery of anti-MMP-13 ribozyme promoted apoptosis in SCC cells within 72 h. Intratumoral injection of anti-MMP-13 ribozyme coding adenovirus into human SCC xenografts established in SCID mice potently suppressed tumor growth, inhibited MMP-13 expression and gelatinolytic activity and reduced the number of proliferating cells within the tumors. These results provide evidence for an important role for MMP-13 in SCC growth and invasion and identify MMP-13 as a promising target for ribozyme-based therapy of SCC in vivo.
引用
收藏
页码:5111 / 5123
页数:13
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