Matrix metalloproteinase inhibitor MMI-166 inhibits lymphogenous metastasis in an orthotopically implanted model of lung cancer

  • Mol Cancer Ther. 2005 Sep;4(9):1409-16. doi: 10.1158/1535-7163.MCT-05-0031.
Haruhiko Fujino  1 Kazuya Kondo Hisashi Ishikura Hideo Maki Hidetaka Kinoshita Takanori Miyoshi Yuji Takahashi Naruhiko Sawada Hiromitsu Takizawa Taeko Nagao Shoji Sakiyama Yasumasa Monden
Affiliations
  • 1. Department of Oncological and Regenerative Surgery, School of Medicine, University of Tokushima, Kuramoto-cho, Japan.
Abstract

Matrix Metalloproteinases (MMP) are considered to be critically involved in tumor invasion and the metastasis of various cancers. MMI-166 is a selective inhibitor of matrix metalloproteinase (MMP-2, MMP-9, and MMP-14). The purpose of this study was to evaluate the effects of MMI-166 on both the growth of the implanted tumor and the lymph node metastasis of the mediastinum and prolonging the life span, using an orthotopic implantation model of the Ma44-3 Cancer cell line. We examined the anti-invasive effect of MMI-166 in lung Cancer cell lines using an in vitro invasion assay. Next, we examined the Anticancer effect of MMI-166 in vivo. MMI-166 (200 mg/kg body weight) or a vehicle was administered orally to the orthotopically implanted lung Cancer model. MMI-166 dose-dependently inhibited the invasion of Cancer cell lines with expressions of MMP-2 and/or MMP-9 in vitro. In vivo, MMI-166 significantly inhibited mediastinal lymph node metastasis in this orthotopic model (weight of the mediastinum: control, 0.089 +/- 0.009 versus MMI-166, 0.069 +/- 0.008 mg; P = 0.005; metastatic area: control, 93,495 +/- 55,747 versus MMI-166, 22,747 +/- 17,478 pixels; P = 0.045). MMI-166 prolonged the life span by 6 days in median survival time in the orthotopically implanted model (P = 0.039). These results showed that MMI-166 could possibly inhibit lymph node metastasis and prolong the life span in lung Cancer patients.

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