Page 212 - AAOMP Onsite Booklet
P. 212

2018 Joint IAOP - AAOMP Meeting


                    Role of matrix metalloproteinases in tumor growth and
                  invasion; focus on Basal cell carcinoma and Squamous cell

                                        carcinoma of head and neck.


                                  Tuesday, 26th June - 16:30 - Stanley Park Ballroom – Salon 2 - Oral



              Dr. rabia safdar (University of Health Sciences, Lahore), Prof. Nadia Naseem (University of Health Sciences Lahore Pakistan), Dr.
                 Varda Jalil (superior university Lahore), Prof. Abdul Hanan Nagi (retired (ex prof of university of health sciences, Lahore))


             OBJECTIVE
              To determine the Matrix metalloproteinase (MMP) 9 & 14 expression in Head and Neck Squamous cell carcinoma
             (HNSCC) and Basal cell carcinoma (BCC) respectively and to determine if there is any relation between MMPs ex-
             pression with HNSCC grade and morphological subtype of BCC.
             FINDINGS
             49 HNSCC & 42 BCC cases were selected. Sections were microscopically scored using scoring criteria by Kamat et
             al: intensity (0-3), proportion (0-3), overall score (intensity+proportion). Tumors were categorized into low and
             high expression groups. Among HNSCC cases, 36.7% showed strong staining intensity of MMP 9 antibody in tumor
             cells, 28.6% showed moderate, 32.7% weak &only 2% showed negative staining, while 51% cases had strong stain-
             ing intensity in stroma adjacent to tumor, 26.5% moderate, 20.4% weak & 2% showed negative staining. For 6.1%
             cases overall expression was weak while 93.9% showed high expression. Statistical relation between histological
             grade & overall expression as well as overall expression for stroma with tumor invading front staining intensity
             were significant by applying Mann-Whitney U test.
             For BCC cases, 47.6% showed strong staining intensity of MMP 14 in tumor cells, 45.2% moderate & 7.1% had weak
             staining intensity while 35.7% cases had strong intensity of MMP 14 antibody staining in stroma, 45.2% moderate
             & 19% cases showed weak staining intensity. Statistical relation between overall expression for tumor & morpho-
             logical grades of BCC & between morphological grade & MMP 14 staining intensity at tumour invading front were
             significant.
             CONCLUSION
             MMPs produced by tumor cells and adjacent stroma play significant role in tumor progression. Our results clearly
             demonstrate marked expression of MMP 9 & 14 in high grade HNSCC & in high risk morphological grades of BCC
             respectively. So targeted therapy protocol for MMPs may represent helpful approach as adjuvant in treatment for
             patients at the initial stages of HNSCC & BCC.

























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