Matrix Metalloproteinases and Cancer - Roles in Threat and Therapy |
Yadav, Lalita
(Department of Oral and Maxillofacial Pathology, Kalka Dental College)
Puri, Naveen (Department of Oral and Maxillofacial Pathology, Kalka Dental College) Rastogi, Varun (Department of Oral and Maxillofacial Pathology, Kalka Dental College) Satpute, Pranali (Department of Oral and Maxillofacial Pathology, Goverment Dental College) Ahmad, Riyaz (GMC) Kaur, Geetpriya (Department of Oral and Maxillofacial Pathology, Kalka Dental College) |
1 | Brew K, Dinakarpandian D, Nagase H (2000).Tissue inhibitors of metalloproteinases: evolution, structure and function. Biochem Biophys Acta, 1477, 267-83. |
2 | Cao Z G, Li C Z (2006). A single nucleotide polymorphism in the matrix metalloproteinase-1 promoter enhances oral squamous cell carcinoma susceptibility in a Chinese population. Oral Oncol, 42, 32-8. DOI |
3 | Chambers A F, Groom A C, Macdonald I C (2002). Dissemination and growth of cancer cells in metastatic sites. Nat Rev Cancer, 2, 563-72. DOI ScienceOn |
4 | Chambers A F, Matrisian L M (1997). Changing views of the role of matrix metalloproteinases in metastasis. J Natl Cancer Inst, 89, 1260-70. DOI ScienceOn |
5 | Overall C M (2002). Molecular determinants of metalloproteinase substrate specificity: matrix metalloproteinases and new 'intracellular substrate binding domains, modules and exosites. Mol Biotechnol Chem, 383, 1059-66. |
6 | Nagase H, Visse R, Murphy G (2006). Structure and function of matrix metalloproteinases and TIMPs. Cardiovascular Res, 69, 562-73. DOI ScienceOn |
7 | Nelson A R, Fingleton B, Rotherberg M L, et al (2000). Matrix metalloproteinases: biologic activity and clinical implications. J Clin Oncol, 18, 1135-49. |
8 | Noe V et al (2001). Release of an invasion promoter E-cadherin fragment by matrilysins and stromilysin-1. J Cell Sci, 114, 111-8. |
9 | Overall C M, Lopez-otin C(2002). Strategies for MMP inhibition in cancer: innovations for the post-trial era. Nat Rev Cancer, 2, 657-72. DOI ScienceOn |
10 | Pendas A M, Balbin M, Llano E, Jimenez M G, Lopez-otin C (1997). Structural analysis and promoter characterization of the human collagenases-3 gene (MMP-13). Genomics, 40, 222-33. DOI ScienceOn |
11 | Uria J A, Ferrando A A, Velasco G, Freije J M P, Lopez-otin C (1994). Structure and expression in breast tumours of human TIMP-3, a new member of the metalloproteinase family. Cancer Res, 54, 2091-94. |
12 | Lockhart A C, Braun R D, Yu D, et al (2003). Reduction of wound angiogenesis in patients treated with BMS-275291, a broad spectrum matrix metalloproteinase inhibitor. Clin Cancer Res, 9, 586-93. |
13 | Lopez-otin C, Overall C M (2002). Protease degradomics: a new challenge for proteomics. Nat Rev Mol Cell Biol, 3, 509-19. DOI |
14 | Manes S, Mira E, Barbacid MM, Cipres A, et al (1997). Identification of insulin -like growth binding protein-1 as a potential physiological substrate for human stromelysins-3. J Biol Chem, 272, 25706-12. DOI ScienceOn |
15 | Lijnen H R (2001). Plasmin and matrix metalloproteinases in vascular remodelling. Thomb Haemost, 86, 324-33. |
16 | Lokeshwar B L, Escatel E, Zhu B (2001). Cytotoxic activity and inhibition of tumour cell invasion by derivatives of a chemically modified tetracycline CMT-3(COL-3). Curr Med Chem, 8, 271-9. DOI |
17 | Maretzky T, Reiss K, Ludwig A, et al (2005). ADAM-10 mediates E-cadherin shedding and regulates epithelial cell-cell adhesion , migration and beta- catenin translocation. Proc Natl Acad Sci USA, 102, 9182-87. DOI |
18 | McCawley L J, Matrisian L M (2001). Matrix metalloproteinases: they are not just for matrix anymore! Curr. Opin. Cell Biol,13, 534-40. DOI ScienceOn |
19 | Mitsiades N, Yu W H, Poulaki V, Tsokos M, Stamenkovic I (2001). Matrix metalloproteinase-7 mediated cleavage of Fas ligand protects tumour cells from chemotherapeutic drug toxicity. Cancer Res, 61, 577-81. |
20 | Egeblad M ,Werb Z (2002). New function for the matrix metalloproteinases in cancer progression. Nature reviews, 2, 161-74. |
21 | Falardeau P, Champagne P, Poyet P, Hariton C, Dupont E (2001). Neovastat, a naturally occurring multifunctional antiangiogenic drug, in phase III clinical trials. Semin Oncol, 28, 620-5. DOI |
22 | Birchmeier C, Birchmeier W, Brand- saberi B (1996). Epithelialmesenchymal transition in cancer progression. ActaAnat, 156, 217-26. |
23 |
Agrez M, Chen A, Cone R I, Pytela R, Sheppard D (1994). The |
24 | Basbaum C B, Werb Z (1996). Focalized proteolysis: spatial and temporal regulation of extracellular matrix at the cell surface. Current Opinions in Cell Biology, 8, 731-38. DOI ScienceOn |
25 | Benbow U, Brinckerhoff C E (1997). The AP-1 site and MMP gene regulation: what is all the fuss about? Matrix Biol, 15, 519-26. DOI ScienceOn |
26 | Sekhon BS (2010). Matrix metalloproteinases-an overview. Res Reports Biol, 1, 20. |
27 | Peschon JJ, Slack JL, Reddy P, et al (1998). An essential role for ectodomain shedding in mammalian development. Science, 282, 1281-84. DOI ScienceOn |
28 | Rundhaung J E. Matrix Metalloproteinases, angiogenesis and cancer (2003). Clin Cancer Res, 9, 551-54. |
29 | Sapadin A N, Fleischmajer R (2006). Tetracyclines: nonantibiotic properties and their clinical implications. J Am Acad Dermatol, 54, 258-65. DOI ScienceOn |
30 | Velasco G, Pendas A M, Fueyo A ,et al (1999). Cloning and characterization of human MMP-23,a new matrix metalloproteinase predominantly expressed in reproductive tissues and lacking conserved domains in other family members. J BiolChem, 274, 4570-76. |
31 | Vihinen P, Kahari V M (2002). Matrix metalloproteinases in cancer: prognostic markers and therapeutic targets. Int J cancer, 99, 157-66. DOI ScienceOn |
32 | Visse R, Nagase H (2003). Matrix metalloproteinases and tissue inhibitors of metalloproteinases: Structure, Function and Biochemistry. Circulation Research, 92,827-39. DOI ScienceOn |
33 | Waldhauer I, Goehlsdorf D, Gieseke F, et al (2008). Tumour associated MICA is shed by ADAM proteases. Cancer Res, 68, 6368-76. DOI ScienceOn |
34 | Westermarck J, Kahari V M (1999). Regulation of matrix metalloproteinase expression in tumour invasion. FASEB J, 13, 781-92. |
35 | Williamson R A, Marston F A, Angal S, et al (1990). Disulphide bond assignment in human tissue inhibitor of metalloproteinases(TIMP). Biochem J, 268, 267-74. |
36 | Jemal A, Tiwari RC, Murray T, et al (2004). Cancer statistics. CA Cancer J Clin, 54, 9-29. |
37 | Murray G I, Duncan M E, O'Neil P, Melvin W T, Fothergill J E (1996). Matrix metalloproteinase-1 is associated with poor prognosis in colorectal cancer. Nat Med, 2, 461-2. DOI |
38 | Kim J, Yu W, Kovalski K, Ossowski L (1998). Requirment of specific proteases in cancer cell intravasation as revealed by a novel semiquantitative PCR based assay. Cell, 94, 353-62. DOI ScienceOn |
39 | Illman S A, Lehti K, Keski-Oja J, Lohi J (2006). Epilysin(MMP-28) induces TGF B mediated epithelial to mesenchymal transition in lung carcinoma cells. J Cell Sci, 119, 3856-65. DOI |
40 | Karin M, Chang L (2001). AP-1 glucocorticoid receptor crosstalk taken to a higher level. J. Endocrinol, 169,447-51. DOI |
41 | Koolwijk P, Sidenius N, Peters E, et al (2001). Proteolysis of the urokinase-type plasminogen activator receptor by metalloproteinase-12:implication for angiogenesis in fibrin matrices. Blood, 97, 3123-31. DOI |
42 | Kousidou O C, Mitropoulou T N, Roussidis A E, et al (2006). Genistein suppresses the invasive potential of human breast cancer cells through transcriptional regulation of metalloproteinases and their tissue inhibitors. Int J Oncol, 26, 1101-9. |
43 | Kuga H, Morisaki T, Nakamura K, et al (2003). Interferon gama suppreses transforming growth factor beta induced invasion of gastric carcinoma cells through cross talk of Smad pathway in a three -dimensional culture model. Oncogene, 22, 7838-47. DOI ScienceOn |
44 | Kumar V, Abbas A K, Fausto N (2004). Robbins and Cotran Pathologic basis of disease. 7thed; Philadelphia; Saunders; Elsevier Inc, 202-3. |
45 | Stamenkovic I (2003). Extracellular remodelling: the role of metalloendopeptidases. J Pathol, 200, 448-64. DOI ScienceOn |
46 | Zhang Y Zhang YY, Chen B, Ding YQ (2012). Metastasisassociated Factors Facilitating the Progression of Colorectal Cancer. APJCP, 13, 2436-47. |
47 | Stetler-Stevenson W G (1999). Matrix metalloproteinases in angiogenesis: a moving target for therapeutic intervention. J Clin Investig, 103, 1237-41. DOI ScienceOn |
48 | Sheu B C, Hsu S M, Ho H N, et al (2001). A novel role of metalloproteinase in cancer-mediated immunosuppression. Cancer Res, 61, 237-42. |
49 | Sternlicht M D, Werb Z (2001). How matrix metalloproteinase regulate cell behaviour. Annu Rev Cell Dev Biol, 17, 463-516. DOI ScienceOn |
50 | Stetler-stevenson W G, Krutzsch H C, Liotta L A (1989). Tissue inhibitor of metalloproteinase (TIMP-2). J BiolChem, 264, 17374-8. |
51 | Steward W P, Thomas A L (2000). Marimastat: the clinical development of a matrix metalloproteinase inhibitor. Expert Opin Invesig Drugs, 9, 2913-22. DOI ScienceOn |
52 | Strickland D K, Ashcom J D, Williams S, et al (1990). Sequence identity between the alpha 2- macroglobulin receptor and low density lipoprotein receptor related protein suggests that this molecule is a multifunctional receptor. J BiolChem, 265, 17401-4. |
53 | Takeichi M (1991). Cadherin cell adhesion receptors as a morphogenetic regulator. Science, 251, 1451-55. DOI |
54 | Thiery J P (2002). Epithelial mesenchymal transitions in tumour progression. Nat Rev Cancer, 2, 442-54. DOI ScienceOn |
55 | Thomas GT, Lewis MP, Speight PM (1999). Matrixmetalloproteinases and oral cancer. Oral Oncol, 227, 33. |
56 | Ganea E, Trifan M, Laslo A C, Putina G, Cristescu C (2007). Matrix metalloproteinases: useful and deleterious. Biochem Soc Trans, 35, 689-91. DOI |
57 | Leco K J, Khokha R, Pavloff N, Hawkes S P, Edwards D R (1994). Tissue inhibitors of metalloproteinases-3 (TIMP-3) is an extracellular matrix associated protein with a distinctive pattern of expression in mouse cells and tissues. J Biol Chem, 269, 9532-60. |
58 | Gialeli C, Theocharis A D, Karamanos N K (2011). Role of matrix metalloproteinases in cancer progression and their pharmacological targeting. FEBS J, 278, 16-27. DOI ScienceOn |
59 | Folgueras A R, Pendas A M, Sanchez L M, Lopez-otin C (2004). Matrix metalloproteinases in cancer: from new function to improved inhibition strategies. Int J Dev Biol, 48, 411-24. DOI |
60 | Gialeli C, Kletsas D, Mavroudis D, Kalofonos H P, Tzanakakis G N (2009). Targetting epidermal growth factor receptor in solid tumours: critical evaluation of the biological importance of therapeutic monoclonal antibodies. Curr Med Chem, 16, 3797-804. DOI |
61 | Gorelik L, Flavell R A (2001). Immune mediated eradication of tumours through the blockage of transforming growth factor-beta signalling in T-cells. Nature Med, 7, 1118-22. DOI ScienceOn |
62 | Greene J, Wang M, Liu Y E, et al (1996). Molecular cloning and characterisation of human tissue inhibitor of metalloproteinase 4. J BiolChem, 271, 30375-380. |
63 | Hanahan D, Folkman J (1996). Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis. Cell, 86, 353-64. DOI ScienceOn |
64 | Hanahan D, Weinberg R A (2000). The hallmarks of cancer. Cell, 100, 57-70. DOI ScienceOn |
65 | Chaudhary A K, Singh M, Bharti A C, et al (2010). Genetic polymorphism of matrix metalloproteinases and their inhibitors in potentially malignant lesions of the head and neck. J Biomed Sci, 17, 10. DOI |
66 | Hidalgo M, Eckhardt S G (2001). Development of matrix metalloproteinase inhibitors in cancer therapy. J Natl Cancer Inst, 93, 178-93. DOI ScienceOn |
67 | Ikebe T, Shinohara M, Takeuchi H, et al (1999). Gelatinolytic activity of matrix metalloproteinase in tumour tissues correlates with invasiveness of oral cancer. Clin Exp Metastasis, 17, 315-23. DOI ScienceOn |
68 | Cornelius L A, et al (1998). Matrix metalloproteinases generate angiostatin: effects on neovascularisation. J Immunol, 161,6845-52. |
69 | Chen L C, Noelken M E, Nagase H(1993). Disruption of the cysteine-75 and zinc ion coordination is not sufficient to activate the precursor of human matrix metalloproteinase 3(stromelysin- 1). Biochemistry, 32, 10289-295. DOI |
70 | Choi S,Myers J N (2008). Molecular pathogenesis of oral squamous cell carcinoma: implications for Therapy. J Dent Res, 87, 14-32. DOI ScienceOn |
71 | Curran S,Murray G I (1999). Matrix metalloproteinases in tumour invasion and metastasis. J Pathol, 189, 300-8. DOI |
72 | Denhardt D T, Feng B, Edwards D R, Cocuzzi E T, Malyanker U M (1993). Tissue inhibitor of metalloproteinases(TIMP aka EPA): structure, control of expression and biological functions. PharmacolTher, 59, 329-341. |
73 | Eccles S A et al (1996). Control of lymphatic and hematogenous metastasis of a rat mammary carcinoma by the matrix metalloproteinase inhibitor batimastat (BB-94). Cancer Res, 56, 2815-22. |
74 | Ferreras M, Felbor U, Lenhard T, Olsen B R, Delaisse J (2000). Generation and degradation of human endostatin protein by various proteinases. FEBS Lett, 486, 247-51. DOI |
75 | Wojtowicz-praga S, Low J, Marshall J, et al (1996). Phase I trial of a novel matrix metalloproteinase inhibitor batimastat(BB-94) in patients with advanced cancer. Invest New Drugs, 14, 193-202. |
76 | Murphy G, Reynolds J J (1993). Extracellular matrix degradation: in connective tissue and its heritable disorders. Royce P M,Steinman B, editors. New York, Wiley-Liss 287-316. |
![]() |