Immunohistochemical expression of Src protein in peripheral and central giant cell granulomas of the jaws

Immunohistochemical expression of Src protein in peripheral and central giant cell granulomas of the jaws


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دانشگاه علوم پزشکی تبریز
دانشگاه علوم پزشکی تبریز

نویسندگان: منیره حلیمی , حامد همیشه کار

کلمات کلیدی: Central giant cell granuloma, immunohistochemistry, peripheral giant cell granuloma, Src

نشریه: 55344 , 3 , 17 , 2013

اطلاعات کلی مقاله
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نویسنده ثبت کننده مقاله منیره حلیمی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه دانشکده پزشکی
کد مقاله 68443
عنوان فارسی مقاله Immunohistochemical expression of Src protein in peripheral and central giant cell granulomas of the jaws
عنوان لاتین مقاله Immunohistochemical expression of Src protein in peripheral and central giant cell granulomas of the jaws
ناشر 5
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نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح دو – PMC
آدرس لینک مقاله/ همایش در شبکه اینترنت

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Aim and Objective: The aim of this study was to investigate the expression of Src protein (an osteoclastic factor) in peripheral and central giant cell granulomas (PGCG and CGCGs) of the jaws and the relationship between the expression of this protein and the clinical behavior of these two lesions. Materials and Methods: Thirty cases of PGCG and 30 cases of CGCG were immunohistochemically stained with Src. A staining‑intensity‑distribution (SID) score (proportion of stained cells × staining intensity) was used to evaluate immunoreactivity of the protein. Data were analyzed using statistical package for social sciences (SPSS) 17.0. Results: There were no significant differences in the Src expression and the SID score between PGCG and CGCG. Furthermore, Spearman’s rank correlation coefficient showed that there was a significant correlation between Src expression and SID score within both PGCG and CGCG (P < 0.001; r = 0.87 and 0.75, respectively). Conclusion: The findings of this study suggest that the multinucleated giant cells share some similarities with osteoclasts and Src protein can be used as a new therapeutic target to inhibit osteoclastic activity. In addition, differences in immunoreactivity of this osteoclastic protein do not reflect different clinical behaviors of PGCG and CGCG.

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نویسنده نفر چندم مقاله
منیره حلیمیسوم
حامد همیشه کارپنجم

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