Review
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World J Biol Chem. Aug 26, 2014; 5(3): 355-376
Published online Aug 26, 2014. doi: 10.4331/wjbc.v5.i3.355
Matrix metalloproteinases and gastrointestinal cancers: Impacts of dietary antioxidants
Sugreev Verma, Kousik Kesh, Nilanjan Ganguly, Sayantan Jana, Snehasikta Swarnakar
Sugreev Verma, Kousik Kesh, Nilanjan Ganguly, Sayantan Jana, Snehasikta Swarnakar, Drug Development Diagnostic and Biotechnology Division, CSIR-Indian Institute of Chemical Biology, Jadavpur, Kolkata 700032, India
Author contributions: All authors contributed to this paper.
Supported by Council of Scientific and Industrial Research, India; (CSIR)-INDEPTH and HUM projects
Correspondence to: Dr. Snehasikta Swarnakar, Drug Development Diagnostic and Biotechnology Division, CSIR-Indian Institute of Chemical Biology, 4 Raja S C Mullick Road, Jadavpur, Kolkata 700032, India. snehasiktas@hotmail.com
Telephone: +91-33-24995824 Fax: +91-33-24735197
Received: April 3, 2014
Revised: May 7, 2014
Accepted: June 10, 2014
Published online: August 26, 2014
Abstract

The process of carcinogenesis is tightly regulated by antioxidant enzymes and matrix degrading enzymes, namely, matrix metalloproteinases (MMPs). Degradation of extracellular matrix (ECM) proteins like collagen, proteoglycan, laminin, elastin and fibronectin is considered to be the prerequisite for tumor invasion and metastasis. MMPs can degrade essentially all of the ECM components and, most MMPs also substantially contribute to angiogenesis, differentiation, proliferation and apoptosis. Hence, MMPs are important regulators of tumor growth both at the primary site and in distant metastases; thus the enzymes are considered as important targets for cancer therapy. The implications of MMPs in cancers are no longer mysterious; however, the mechanism of action is yet to be explained. Herein, our major interest is to clarify how MMPs are tied up with gastrointestinal cancers. Gastrointestinal cancer is a variety of cancer types, including the cancers of gastrointestinal tract and organs, i.e., esophagus, stomach, biliary system, pancreas, small intestine, large intestine, rectum and anus. The activity of MMPs is regulated by its endogenous inhibitor tissue inhibitor of metalloproteinase (TIMP) which bind MMPs with a 1:1 stoichiometry. In addition, RECK (reversion including cysteine-rich protein with kazal motifs) is a membrane bound glycoprotein that inhibits MMP-2, -9 and -14. Moreover, α2-macroglobulin mediates the uptake of several MMPs thereby inhibit their activity. Cancerous conditions increase intrinsic reactive oxygen species (ROS) through mitochondrial dysfunction leading to altered protease/anti-protease balance. ROS, an index of oxidative stress is also involved in tumorigenesis by activation of different MAP kinase pathways including MMP induction. Oxidative stress is involved in cancer by changing the activity and expression of regulatory proteins especially MMPs. Epidemiological studies have shown that high intake of fruits that rich in antioxidants is associated with a lower cancer incidence. Evidence indicates that some antioxidants inhibit the growth of malignant cells by inducing apoptosis and inhibiting the activity of MMPs. This review is discussed in six subchapters, as follows.

Keywords: Gastrointestinal cancer, Matrix metalloproteinase, Tissue inhibitor of matrix metalloproteinases, Reactive oxygen species, Antioxidants

Core tip: Matrix metalloproteinases (MMPs), a group of zinc dependent endopeptidases, substantially contribute to extra cellular remodelling, angiogenesis, cellular differentiation, proliferation and apoptosis. MMPs are also important regulators of tumor growth both at the primary site and in distant metastasis; thus the enzymes are considered as important targets for cancer therapy. This review describes the roles and regulation of different MMPs and their subsequent actions over different gastrointestinal cancers both in epigenetic and cellular level. Furthermore, this review summarizes the current state of knowledge of dietary antioxidants in preventing gastrointestinal cancer progression as well as mechanism of action.