Literature DB >> 19445018

Matrix metalloproteinase-2 expression in stromal tissues is a consistent prognostic factor in stage II colon cancer.

Yoshiko Inafuku1, Tomohisa Furuhata, Makoto Tayama, Kenji Okita, Toshihiko Nishidate, Toru Mizuguchi, Yasutoshi Kimura, Koichi Hirata.   

Abstract

For patients with stage II colon cancer, the usefulness of adjuvant chemotherapy remains controversial. Therefore, it is important to identify high-risk indicators. The biological prognostic factors for recurrence might allow further insight into the optimal treatment strategy for patients with node-negative disease. Matrix metalloproteinase-2 seems to be one of the essential factors for tumor invasion and lymph node metastasis. In this study, we analyzed the expression of cyclooxygenase-2 and matrix metalloproteinase-2 by immunohistochemical staining in 109 patients with stage II colon cancer. A positive correlation was observed between tumor cyclooxygenase-2 and tumor matrix metalloproteinase-2 expression (P = 0.0006) and between tumor cyclooxygenase-2 and stromal matrix metalloproteinase-2 expression (P < 0.0001). Stromal matrix metalloproteinase-2 expression was associated with disease-free survival (P = 0.0095) and was shown to be an independent risk factor for recurrence by multivariate analysis. In addition, we carried out an invasion assay in vitro to investigate whether cyclooxygenase-2 and matrix metalloproteinase-2 affected the tumor-invasive potential of colon cancer cell lines. The invasion assay showed that every cancer cell line acquired invasive potential in coculture with stromal cell lines and the cyclooxygenase-2 inhibitor suppressed this phenomenon by downregulating the matrix metalloproteinase-2 expression of stromal cells. In conclusion, these findings suggest that matrix metalloproteinase-2 expression in stromal cells can be a high-risk indicator for recurrence in patients with stage II colon cancer.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19445018     DOI: 10.1111/j.1349-7006.2009.01116.x

Source DB:  PubMed          Journal:  Cancer Sci        ISSN: 1347-9032            Impact factor:   6.716


  4 in total

1.  Inactivation of chemokine (C-C motif) receptor 1 (CCR1) suppresses colon cancer liver metastasis by blocking accumulation of immature myeloid cells in a mouse model.

Authors:  Takanori Kitamura; Teruaki Fujishita; Pius Loetscher; Laszlo Revesz; Hiroki Hashida; Shinae Kizaka-Kondoh; Masahiro Aoki; Makoto M Taketo
Journal:  Proc Natl Acad Sci U S A       Date:  2010-06-29       Impact factor: 11.205

2.  Role of pancreatic stellate cells in pancreatic cancer metastasis.

Authors:  Zhihong Xu; Alain Vonlaufen; Phoebe A Phillips; Eva Fiala-Beer; Xuguo Zhang; Lu Yang; Andrew V Biankin; David Goldstein; Romano C Pirola; Jeremy S Wilson; Minoti V Apte
Journal:  Am J Pathol       Date:  2010-10-07       Impact factor: 4.307

3.  MiR-650 represses high-risk non-metastatic colorectal cancer progression via inhibition of AKT2/GSK3β/E-cadherin pathway.

Authors:  Chunxian Zhou; Fengyun Cui; Jiali Li; Diyi Wang; Yingze Wei; Ying Wu; Jiping Wang; Hongguang Zhu; Shuyang Wang
Journal:  Oncotarget       Date:  2017-07-25

4.  Prognostic significance of COX-2 immunohistochemical expression in colorectal cancer: a meta-analysis of the literature.

Authors:  Ling Peng; Yun Zhou; Yina Wang; Haibo Mou; Qiong Zhao
Journal:  PLoS One       Date:  2013-03-20       Impact factor: 3.240

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.