Activation of MMP-2 and MMP-9 in patients with oral squamous cell carcinoma
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Patel, BP
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机构:Gujarat Canc Soc, Div Res, Biochem Res Sect, Ahmadabad 380016, Gujarat, India
Patel, BP
Shah, PM
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机构:Gujarat Canc Soc, Div Res, Biochem Res Sect, Ahmadabad 380016, Gujarat, India
Shah, PM
Rawal, UM
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机构:Gujarat Canc Soc, Div Res, Biochem Res Sect, Ahmadabad 380016, Gujarat, India
Rawal, UM
Desai, AA
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机构:Gujarat Canc Soc, Div Res, Biochem Res Sect, Ahmadabad 380016, Gujarat, India
Desai, AA
Shah, SV
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机构:Gujarat Canc Soc, Div Res, Biochem Res Sect, Ahmadabad 380016, Gujarat, India
Shah, SV
Rawal, RM
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机构:Gujarat Canc Soc, Div Res, Biochem Res Sect, Ahmadabad 380016, Gujarat, India
Rawal, RM
Patel, PS
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Gujarat Canc Soc, Div Res, Biochem Res Sect, Ahmadabad 380016, Gujarat, IndiaGujarat Canc Soc, Div Res, Biochem Res Sect, Ahmadabad 380016, Gujarat, India
Patel, PS
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机构:
[1] Gujarat Canc Soc, Div Res, Biochem Res Sect, Ahmadabad 380016, Gujarat, India
[2] Gujarat Canc Res Inst, Dept Surg Oncol, Ahmadabad, Gujarat, India
[3] Gujarat Canc Res Inst, Div Biochem Res, Ahmadabad, Gujarat, India
[4] Gujarat Univ, Sch Sci, Dept Zool, Ahmadabad, Gujarat, India
Background and Objectives: Oral cancer accounts for one third of all malignancies in India where habit of tobacco consumption is the major etiologic factor, which causes field cancerization in oral mucosa. Multiple molecular events in oral mucosa due to field cancerization may be the cause of local and regional lymph node involvement in oral cancer resulting into low overall survival, high recurrence rate, and poor prognosis. Several matrix metalloproteinases (MMPs) have been shown to play an important role in the invasion and metastasis of oral squamous cell carcinoma (SCC). MMP-2 and MMP-9 are capable of degrading type-IV collagen, which is a major component of basement membrane. Therefore, we studied MMP-2 and MMP-9 activation by gelatin zymography, which is cost effective alternate to ELISA method, in patients with oral SCCs to predict their role in metastatic potentials. Materials and Methods: Thirty-nine patients of oral SCCs were classified as non-metastatic (n = 28), and metastatic (n = 11) according to regional lymph node involvement. Malignant and adjacent normal tissues of the patients Were collected at the time of surgery. Gelatin zymography was carried out using 7.5% polyacrylamide gel under non-denaturing and non-reducing conditions. Zymograms were analyzed densitometrically. Latent and active forms of MMP-2 and MMP-9 were expressed as ng/50 mug of protein. Results: Latent and active forms of MMP-2 and MMP-9 were significantly elevated in malignant tissues as compared to their adjacent normal tissues (P < 0.05). Total MMP-2 and MMP-9 activities were also significantly elevated in malignant tissues as compared to adjacent normal tissues (P = 0.005 and P = 0.028, respectively). Activation ratio of MMP-2 and MMP-9 were significantly elevated in malignant tissues as compared to adjacent normal tissues. Activation of MMP-2 was prominent (11%) than MMP-9 (5%) in malignant tissues. Activation ratio of MMP-2 was significantly elevated in patients with lymph node metastasis than patients without lymph node metastasis (P=0.005). Receiver's operating characteristic (ROC) curve analysis revealed that activation ratio of MMP-2 discriminate better than and activation ratio of MMP-9 between patients with and without lymph not le metastasis. Activation ratio of MMP-2 could predict risk of lymph node metastasis development in patients without lymph node involvement. Conclusion: The study concluded that activation of MMP-2 and MMP-9 was significantly higher in malignant tissues as compared to adjacent normal tissues. Further, activation ratio of MMP-2 was significantly elevated in patients with lymph node metastasis as compared to patients Without lymph node metastasis, which could predict risk of lymph node metastasis development in node negative patients. (C) 2005 Wiley-Liss, Inc.
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Mil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, SerbiaMil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia
Rasic, Dejan
Peric, Aleksandar
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Mil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia
Univ Def, Fac Med Mil Med Acad, Belgrade, SerbiaMil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia
Peric, Aleksandar
Djurdjevic, Biserka Vukomanovic
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Mil Med Acad, Inst Pathol, Belgrade, Serbia
Univ Def, Fac Med Mil Med Acad, Belgrade, SerbiaMil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia
Djurdjevic, Biserka Vukomanovic
Sotirovic, Jelena
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Mil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia
Univ Def, Fac Med Mil Med Acad, Belgrade, SerbiaMil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia
Sotirovic, Jelena
Baletic, Nenad
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Mil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia
Univ Def, Fac Med Mil Med Acad, Belgrade, SerbiaMil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia
Baletic, Nenad
Milojevic, Milanko
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Mil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia
Univ Def, Fac Med Mil Med Acad, Belgrade, SerbiaMil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia
Milojevic, Milanko
Pavicevic, Ljubomir
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Mil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, SerbiaMil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia
Pavicevic, Ljubomir
Dimic, Aleksandar
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Mil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, SerbiaMil Med Acad, Clin Otorhinolaryngol, Crnotravska 17, Belgrade 11000, Serbia