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Background. Regeneration of bone defects remains a challenge for maxillofacial surgeons. The present study aimed to compare the effects of octacalcium phosphate (OCP) and the combination of octacalcium phosphate/gelatin (OCP/Gel) on mandibular bone regeneration in rats Methods. In the present study, 36 male Sprague-Dawley rats were used. The animals were randomly assigned to the following experimental groups: OCP (n=12), OCP/Gel (n=12), and the control group (n=12). Defects were created in the rat mandibles and filled with 10 mg of OCP and OCP/Gel disks in the experimental groups. In the control group, however, no substance was administered. Samples were taken on days 7, 14, 21 and 56, respectively, after the implantation. Sections (5 µ) were prepared and stained by H&E. The sections were studied, and the volume fraction of newly formed bone was measured by Dunnett's T3 test based on the significance level (P=0.05). Results. In the experimental groups, the new bone formation began from the margin of defects 7‒14 days after the implantation. During the healing process, the newly formed bone healed a larger area of the defects and grew structurally. In the control group, the defects were primarily filled with dense connective tissue, and only a small amount of new bone was formed. The present study showed a statistically significant difference in the volume of newly formed bone between the experimental groups and the control group (PConclusion. OCP/Gel composite can be beneficial in the healing process of mandibular bone defects.

Background: Lung cancer has the highest frequency among cancers worldwide. It is the leading cause of cancer-induced death in industrialized countries. Abnormal glycosylation of cell surface and extracellular matrix glycoconjugates are among the most critical issues in neoplasia. Objectives: This present study aimed to detect N – acetyl glucosamine (GlcNac) and L- fucose (L-fuc) containing glycoconjugates in lung cancer. Methods: In this cross-sectional study, we selected paraffin blocks belonging to 25 patients with lung cancer from their pathology files at the Ali-Ebne Abitaleb Hospital, Zahedan, Iran. Six µm sections were obtained from the blocks and stained with Hematoxylin-Eosin (H-E) and lectin histochemistry (UEA and SBA lectins). Alcian Blue pH 2.5 was used as a counterstain; lectins were diluted up to 10µg/ml, and DAB was used as a chromogen. Histochemical grading was conducted blindly according to staining intensity to lectins (0-3). The data was collected and analyzed by the Mann-Whitney U test, using SPSS. Results: Statistical analysis showed that there was a significant difference between inflammatory mucosa of the bronchial tree and all types of lung cancer (i.e., adenocarcinoma and squamous cell carcinoma, as well as small and large cell lung carcinoma) according to staining intensity to SBA and UEA lectins (P < 0.001). Our results showed that there were many different patterns of reaction to SBA and UEA lectins between all types of lung cancer cells and epithelial cells of the bronchial tree. Conclusions: Staining intensity and pattern of reaction to lectins were different between all types of lung cancer cells and epithelial mucosa.