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1.
Chinese Journal of Stomatology ; (12): 600-605, 2013.
Article in Chinese | WPRIM | ID: wpr-274193

ABSTRACT

<p><b>OBJECTIVE</b>To develop a child craniofacial three-dimensional (3D) finite element model (FEM) with sutures defined alone.</p><p><b>METHODS</b>The CT data for this study was developed from sequential computed tomography scan images taken at 0.625 mm intervals of an 8 years children skull. Data set was imported into Mimics 10.0 and processed with Geomagic 9.0, and exported as initial graphics exchange specification(IGES) files. The IGES files were then imported into Ansys 13.0 to set up two FEM with or without the median palatine suture being opened. The FEM contained nine craniofacial sutures and eight teeth which were defined alone.For simulating orthopedic maxillary protraction, three forces (F1-F2) were loaded on FEM.F1(1 N) was loaded at 1 cm above the geison. F2(1 N) was loaded at articular fossa of temporal bone. F3(2 N) was directed anteriorly and paralleled with occlusal plane near the canine. The stress distribution and the values distributed in each point gained in the two models were compared.</p><p><b>RESULTS</b>Two craniofacial 3D FEM of the child were developed with the median palatine suture opened or not .With median palatine suture being opened or not, the two models showed the similar von Mises stresses (VMS). The distribution of the VMS was in the bridge of the nose and dextro-ala nasi.When the median palatine suture was opened, the max VMS value was 18916.00×10(-4) MPa which appeared in the nose point and the min VMS value was 1.61×10(-4) MPa which appeared in the maxillary central incisor point. At the same time, the max stress value at the direction Y was -3985.30×10(-4) MPa and appeared in the frontomaxillary suture point, and the min Y value was 0.08×10(-4) MPa which appeared in the maxillary central incisor point. When the median palatine suture was not opened, the max VMS value was 19 244.00×10(-4) MPa and appeared in the nose point. The min VMS value was 1.62×10(-4) MPa and appeared in the maxillary central incisor point. At the same time, the max stress value at the direction Y was -4258.20×10(-4) MPa and appeared in the frontomaxillary suture point, and the min Y value was 0.08×10(-4) MPa which appeared in the maxillary central incisor point.</p><p><b>CONCLUSIONS</b>To define the sutures as entities alone contributed to develop child craniofacial 3D FEM which consist nine sutures. There was tiny difference in stress distribution in both the VMS and in Y direction with the median palatine suture being opened or not.</p>


Subject(s)
Child , Humans , Male , Cephalometry , Methods , Computer Simulation , Cranial Sutures , Physiology , Dental Stress Analysis , Methods , Finite Element Analysis , Imaging, Three-Dimensional , Models, Biological , Skull , Diagnostic Imaging , Stress, Mechanical , Tomography, Spiral Computed
2.
West China Journal of Stomatology ; (6): 27-30, 2011.
Article in Chinese | WPRIM | ID: wpr-350244

ABSTRACT

<p><b>OBJECTIVE</b>To observe the effect of mini-implant lengths on stress distribution in peri-implant surface.</p><p><b>METHODS</b>The 3D finite element analysis mandible and mini-implant models with diameter of 1.6 mm, lengths of 6, 8, 10 and 12 mm were established. The mini-implants were inserted into designed site of mandibular vertically, respectively. A force of 1.96 N were applied mesioly and 45 degrees tilted mesio-vertically in models. The stress distribution under every condition was recorded and analyzed.</p><p><b>RESULTS</b>When load was applied mesially, the maximum stress varied from 3.500 to 3.765 MPa, the maximum displacement varied from 1.266 to 1.288 microm. When load was applied 45 degrees tilted mesio-vertically, the maximum stress varied from 4.075 to 4.510 MPa, the maximum displacement varied from 1.668 to 1.694 microm. All of the maximum stress and displacement of loading mesially were lower than loading mesio-vertically.</p><p><b>CONCLUSION</b>The change of the mini-implant length within 6-12 mm don't show much influence on the stress distribution. The loading type is an important factor influencing stress and displacement of peri-implant bone.</p>


Subject(s)
Humans , Dental Prosthesis Design , Dental Stress Analysis , Finite Element Analysis , Mandible
3.
Chinese Journal of Stomatology ; (12): 20-25, 2010.
Article in Chinese | WPRIM | ID: wpr-245252

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of down-regulated proteoglycans on the proliferation of human salivary adenoid cystic carcinoma (SACC).</p><p><b>METHODS</b>The short hairpin RNA (shRNA) plasmid silencing human xylosyltransferase-I (XT-I) gene was constructed and named shRNA-WJ3. Adenoid cystic carcinoma cells with high metastatic tendency (ACC-M) were transfected by shRNA-WJ3. The plasmid shRNA-HK not targeting any human gene was transfected into ACC-M cells used as negative control. After 48 h of transfection, the positive cells were screened by G418 to isolate the stable transfected cells. Real-time PCR and Western blotting were used to test the gene silence, and the proteoglycans contents of the cells were detected. The stable cell line silenced XT-I was named ACC-M-WJ3. MTT assay was performed to detect the cell proliferation. The cell cycle was analyzed by flow cytometry.</p><p><b>RESULTS</b>ShRNA-WJ3 showed powerful RNA interference and gene silence of XT-I. The inhibition rate was 83.70% of mRNA expression and 79.60% of protein expression respectively. The content of proteoglycans in ACC-M-WJ3 was down-regulated by 49.71%-54.59%. The results of MTT assay showed that the cell growth was inhibited significantly. S phrase decreased and G₁-G₀ phrase increased in group ACC-M-WJ3 compared with that of group ACC-M-HK (P < 0.05).</p><p><b>CONCLUSIONS</b>The down-regulated proteoglycans could inhibit the proliferation of human ACC-M cells.</p>


Subject(s)
Humans , Carcinoma, Adenoid Cystic , Genetics , Metabolism , Pathology , Cell Cycle , Cell Line, Tumor , Cell Proliferation , Down-Regulation , Gene Silencing , Pentosyltransferases , Genetics , Metabolism , Proteoglycans , Metabolism , RNA, Messenger , Metabolism , RNA, Small Interfering , Salivary Gland Neoplasms , Genetics , Metabolism , Pathology , Transfection
4.
Chinese Journal of Stomatology ; (12): 31-35, 2010.
Article in Chinese | WPRIM | ID: wpr-245249

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of traditional Chinese medicine on the differentiation of mesenchymal stem cells (MSC) to osteoblasts.</p><p><b>METHODS</b>Six male Beagle dogs weighed 10-15 kg each were divided into three groups, group A: medicine serum group, group B: non-medicine serum group and group C: bovine serum group. The serum of group A was obtained from the femoral artery of 2 Beagle dogs drinking equivalent dose of traditional Chinese medicine according to body surface area for 7 continuous days. The serum of group B was collected from the femoral artery of 2 Beagle dogs fed with equal volume of normal saline for 7 days. The serum of group C was fetal bovine serum. The tibia marrow was harvested from another 2 Beagle dogs and MSC were isolated and purified by density gradient centrifugation. MSC were cultured in DMEM solution with fetal bovine serum. After MSC were digested by trypsin, MSC were cultured in DMEM solution with the osteogeneic inducer, which contained dexamethasone, antiscorbutic and beta-glycerophosphate. Morphological and histological changes of the MSC were observed under an inverted microscope. Alizarin monosulfonate and nitric acid argentum staining was performed to observe the calcium deposition. MSC were curtured in DMED solution with medicine serum (group A), non-medicine serum (group B) and bovine serum (group C) respectively. The growth curve was detected by the methyl thiazolyl tetrazolium (MTT). The alkaline phosphatase (ALP) activities were detected to observe the differentiation of MSC.</p><p><b>RESULTS</b>The original MSC were observed as fibroblast-like cell shapes. After the osteogeneic inducer was added, MSC were polygon cells with a few polyprocess. Calcium deposition appeared during 10-14 days and alizarin monosulfonate and Von Kossa staining presented positive. MTT results showed that the number of adherent cells of group A was more than that of group B and that of group C significantly after 6 days (P < 0.05). ALP detection proved that ALP activity of group A was more than that of group B and that of group C significantly after 5 days (P < 0.05).</p><p><b>CONCLUSIONS</b>The traditional Chinese medicine promotes the differentiation of MSC to osteoblasts and osteogenesis.</p>


Subject(s)
Animals , Dogs , Male , Alkaline Phosphatase , Metabolism , Cell Differentiation , Cells, Cultured , Drug Combinations , Drugs, Chinese Herbal , Pharmacology , Medicine, Chinese Traditional , Mesenchymal Stem Cells , Cell Biology , Metabolism , Osteoblasts , Cell Biology , Osteogenesis
5.
West China Journal of Stomatology ; (6): 178-182, 2009.
Article in Chinese | WPRIM | ID: wpr-248278

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the effectiveness of treatment with maxillary protraction with or without rapid palatal expansion (RPE) for skeletal Class III malocclusion in mixed dentition.</p><p><b>METHODS</b>A total of 31 children with Class III malocclusion in mixed dentition were selected, and 15 (group A) received maxillary protraction treatment with RPE, the other 16 (group B) received maxillary protraction without RPE. Cephalometric films were taken before and after treatment, and traditional and Pancherz analysis were used.</p><p><b>RESULTS</b>The average duration of treatment was 10.14 months in group A and 9.77 months in group B respectively (P>0.05). According to Pancherz analysis, maxillary basal bone moved forwards by 2.99 mm in group A and 3.33 mm in group B respectively (P>0.05), mandibular basal bone moved backwards by 0.07 mm in group A, while forwards by 0.80 mm in group B (P>0.05), the overjet increased by 4.51 mm in group A and 6.37 mm in group B respectively (P<0.05), and the molar relationship improved by 4.97 mm in group A and 4.73 mm in group B respectively (P>0.05). The effects were clinically satisfactory in the both groups. Lower molar moved forwards by 1.18 mm in basal bone in group A, while backwards by 1.20 mm in group B (P<0.05). Traditional cephalometric analysis showed no statistic differences between the two groups except that upper incisior showed greater procline in group B than in group A (P<0.05).</p><p><b>CONCLUSION</b>The study shows that maxillary protraction treatment, with or without RPE, is clinically satisfactory to correct early skeletal Class III malocclusion.</p>


Subject(s)
Child , Female , Humans , Male , Cephalometry , Extraoral Traction Appliances , Malocclusion, Angle Class III , Mandible , Maxilla , Molar , Palatal Expansion Technique
6.
Chinese Journal of Stomatology ; (12): 113-117, 2008.
Article in Chinese | WPRIM | ID: wpr-235971

ABSTRACT

<p><b>OBJECTIVE</b>To examine the effects of H-ras gene silence on cell cycle, proliferation and apoptosis of salivary adenoid cystic carcinoma -M (SACC-M) cell lines.</p><p><b>METHODS</b>The plasmid H-ras-shRNA, containing the sequence of shRNA targeting H-ras, and HK-shRNA (without interfering effect) were constructed and transfected into SACC-M cells. The cell line with shRNA plasmid stable expression was isolated by G418. The expression levels of H-ras were detected by RT-PCR and protein immunofluorescent assay; cell cycle and cell apoptosis were analyzed by flow cytometry (FCM). The proliferation of cell was also determined by subcutaneous tumor formation in nude mice.</p><p><b>RESULTS</b>After transfection of H-ras-shRNA plasmid, the mRNA expression of H-ras in SACC-M cells was down-regulated by 61.80% and protein expression of H-ras was inhibited by 62.76%; the cell proliferation was inhibited obviously; the G0G1 phase cells were increased. The cell apoptosis rate of H-ras-shRNA group was significantly higher than that of HK-shRNA group (P <0.05). The volume of subcutaneous tumor in nude mice was significantly smaller in Hras-shRNA group than in control group.</p><p><b>CONCLUSIONS</b>The recombinant plasmid HRAS-shRNA could efficiently down-regulate the expression of H-ras gene and protein, induce apoptosis of SACC-M cells and simultaneously inhibit proliferation of these cells in vitro and in vivo.</p>


Subject(s)
Animals , Female , Humans , Mice , Apoptosis , Carcinoma, Adenoid Cystic , Genetics , Pathology , Cell Line, Tumor , Cell Proliferation , Gene Silencing , Mice, Inbred BALB C , Mice, Nude , Proto-Oncogene Proteins p21(ras) , Genetics , RNA, Small Interfering , Genetics , Salivary Gland Neoplasms , Genetics , Pathology , Transfection
7.
Chinese Journal of Stomatology ; (12): 546-550, 2008.
Article in Chinese | WPRIM | ID: wpr-251006

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of rapid canine distalization through distraction of the periodontal ligament after reducing interseptal bone resistance.</p><p><b>METHODS</b>Twenty canines in 11 patients who needed first premolar extractions were involved. A tooth-borne, custom-made distractor was bonded right after the first premolar extraction and the interseptal bone resistance reduction. Three days post-operatively, the distractor was activated 0.1 mm three times a day. Orthodontic models, panoramic radiographs, periapical radiographs, electrical vitality test were assessed pre- and post distraction procedure and 3 months after the completion of the procedure.</p><p><b>RESULTS</b>The distraction procedure was completed in 18 to 35 days [mean (25.6 +/- 4.7) days], with the distal displacement of the canines ranging from 3.53 to 8.29 mm [mean (5.56 +/- 1.32) mm]. The canines showed a mean of 12.20 degrees distal tipping and 18.53 degrees rotation. The anchorage teeth showed an average of (0.76 +/- 0.75) mm mesial movement. The mesial contact point of incisors showed a mean of (0.67 +/- 0.55) mm lingual movement. There was no significant root resorption or long-time change on pulp vitality after distraction.</p><p><b>CONCLUSIONS</b>The canine distalization through distraction of the periodontal ligament after reducing interseptal bone resistance was an effective approach to move canines rapidly.</p>


Subject(s)
Adolescent , Female , Humans , Male , Cuspid , General Surgery , Periodontal Ligament , General Surgery , Root Resorption , General Surgery , Tooth Movement Techniques , Methods
8.
West China Journal of Stomatology ; (6): 22-28, 2007.
Article in Chinese | WPRIM | ID: wpr-249765

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the activity of DNA polbeta promoter on p53 gene in salivary adenoid cystic carcinoma (SACC) cells.</p><p><b>METHODS</b>The luciferase activity was examined and used to evaluate the activity of DNA polbeta promoter on SACC-83 cells. Eukaryotic expression plasmids of p53 gene were constructed and stably transfected into SACC-83 cells. RT-PCR was used to assess the expression of p53 gene. The SACC-83 cells were subjected to the treatments of H2O2, ultraviolet radiation, Bleocin, and affected p53 mRNA and protein level in SACC-83 cells were characterized with RT-PCR and Western blotting.</p><p><b>RESULTS</b>The result of luciferase activity proved that the activity of DNA polbeta promoter in SACC-83 cells was much higher than that of CMV promoter. The results of RT-PCR suggested that p53 gene with different promoters were all expressed effectively, but the expression efficiency was different. It was greater in DNA polbeta group than in CMV group. After DNA damage, p53 gene expression increased and DNA polbeta promoter could enhance the expression of p53 gene more than CMV promoter. The results of Western blotting indicated that the expression of P53 protein between the two groups did not show any difference.</p><p><b>CONCLUSION</b>In SACC cells, the activity of DNA polbeta promoter was increased and DNA polbeta promoter could enhance the expression of p53.</p>


Subject(s)
Humans , Carcinoma, Adenoid Cystic , Cell Line, Tumor , DNA , Genes, p53 , Hydrogen Peroxide , Promoter Regions, Genetic , RNA, Messenger , Salivary Gland Neoplasms , Transfection , Ultraviolet Rays
9.
Chinese Journal of Stomatology ; (12): 144-147, 2007.
Article in Chinese | WPRIM | ID: wpr-333383

ABSTRACT

<p><b>OBJECTIVE</b>To analyze the original mutated codon of p53 gene of salivary pleomorphic adenoma (SPA) and to evaluate the repair effects of wt-p53 on SPA cells.</p><p><b>METHODS</b>Four cases of SPA were obtained from clinical fresh samples and SPA cells were separated and cultured, and then the cells were transduced by Ad-wt-p53. The cells and the corresponding tumor tissue DNA were extracted, PCR and single strand conformational polymorphism (SSCP) and DNA sequencing analysis were performed.</p><p><b>RESULTS</b>PCR-SSCP analysis showed 3 out of 4 SPA with abnormal exon 8 and abnormal exon 6. DNA sequencing analysis showed that exon 6 point mutation was found at codon 203 (GTG-->GCG), poly-codon mutations were found in exon 8 at codon 272 (GTG-->GT square), 275 (TGT-->T square T), 276 (GCC--> square CC) and at codon 290 (CGC-->CGCC). After transduced by Ad-wt-p53, all of the mutated codons were repaired.</p><p><b>CONCLUSIONS</b>p53 gene mutation involved many codons that occurred frequently in the tumorigenesis of SPA. Exogenous wt-p53 could compensate and repair all the mutated p53 codons of SPA cells. SPA cells transduced by Ad-wt-p53 showed the typical apoptosis.</p>


Subject(s)
Humans , Adenoma, Pleomorphic , Genetics , DNA Repair , Mutation , Polymorphism, Single-Stranded Conformational , Salivary Gland Neoplasms , Genetics , Transfection , Tumor Cells, Cultured , Tumor Suppressor Protein p53 , Genetics
10.
Chinese Journal of Stomatology ; (12): 373-377, 2007.
Article in Chinese | WPRIM | ID: wpr-333316

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the expression of dental matrix protein-l (DMP1) in porcine oral mucosa fibroblasts (POMF) transfected by DMP1 and the influences of the transfection.</p><p><b>METHODS</b>The full length of porcine DMP1 cDNA was linked into an eukaryotic expression vector pEGFP-C1. POMF and mesenchymal stem cells (MSC) were transfected with the pEGFP-DMP1. The expression of DMP1, dental sialoprotein (DSP), amelin and ameloblastin (Ambn) gene of transfected POMF and MSC were detected by RT-PCR. The expression of DMP1 and DSP protein was examined by immunocytochemical staining. The formation ratio of mineralized nodules of transfected cells was compared with un-transfected ones after mineralized induction. The formation of mineralized nodules of three-dimensional pellet transfected cells was compared with un-transfected ones after hematoxylin and eosin staining.</p><p><b>RESULTS</b>The constructed pEGFP-DMP1 could produce 4.7 kb and 1.5 kb fragments. DMP1 gene, DSP gene and Ambn gene were expressed by POMF after transfection. Immunohistochemical staining and the quantitative analysis of protein showed that DMP1 and DSP protein was positive in transfected POMF and MSC. The formation ratio of mineralized nodules of transfected POMF and MSC was higher than that of un-transfected ones (P < 0.05).</p><p><b>CONCLUSIONS</b>The expression of porcine DMP1 in POME after gene transfection can induce the expression of tooth-development-associated gene Ambn and DSP and enhance the formation of mineralized nodules.</p>


Subject(s)
Animals , Calcification, Physiologic , Cell Differentiation , Cells, Cultured , Extracellular Matrix Proteins , Genetics , Metabolism , Fibroblasts , Cell Biology , Metabolism , Genetic Vectors , Mouth Mucosa , Cell Biology , Phosphoproteins , Genetics , Metabolism , Swine , Transfection
11.
West China Journal of Stomatology ; (6): 349-353, 2007.
Article in Chinese | WPRIM | ID: wpr-348051

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the imagery changes of the upper airway and the surrounding soft tissues of local adults with non-apnea who used snore guard and to provide experimental data for the clinical diagnosis and treatment of obstructive sleep apnea syndrome (OSAS).</p><p><b>METHODS</b>Thirty students with non-apnea from Hebei medical university were chosen, and magnetic resonance imaging (MRI) was used to measure the changes of the upper airway and the surrounding soft tissues after snore guards were used. SPSS 105 software was used to analyze statistically.</p><p><b>RESULTS</b>After the snore guard was put into oral cavity, the change of the average section and volume of the nasopharynx, the palatopharynx, the hypopharynx and the glossopharynx were statistically significant. The average sagittal size, the average horizontal size of the nasopharynx, the palatopharynx, the hypopharynx and the glossopharynx were increased statistically. The ratio of sagittal size, the horizontal sizand the in the hypopharynx and the glossopharynx changed statistically important. There was a decrease of the soft palate, the shape, the height, and the length of the tongue, the difference was statistically significant. The results demonstrated that snore guard affected the upper airway mainly by changing the volume and the shape of the upper airway, there was an obvious increase of the pharynx. The results also showed that snore guard could increase the width (both sagittal and horizontal) of the upper airway and could change the shape of the surrounding soft tissues, which caused air way more smooth. Snore guard could make the indexes of soft palate and tongue change decreasingly, resulted in the straight stand up of the tongue and the forwardness of the soft palate.</p><p><b>CONCLUSION</b>Snore guard is an effective and convenient instrument for treating the patients with OSAS.</p>


Subject(s)
Adult , Humans , Male , Dental Occlusion , Magnetic Resonance Imaging , Palate, Soft , Pharynx , Sleep Apnea, Obstructive , Tongue
12.
Chinese Journal of Stomatology ; (12): 45-48, 2006.
Article in Chinese | WPRIM | ID: wpr-303437

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the inhibitory effect of p53 gene on salivary adenoid cystic carcinoma (SACC) cells.</p><p><b>METHODS</b>Adenoviral vector pDeltaE1-p53 was constructed and transfected into SACC-83 cells. The enhanced p53 expression was measured by reverse transcription polymerase chain reaction (RT-PCR), and the effects of transfected p53 on SACC-83 cells were analyzed by TRAP-PCR-ELISA, luciferase reporter, flow cytometry (FCM), soft agar assay and tumorigenicity test.</p><p><b>RESULTS</b>The expression of p53 gene in SACC-83 cells was increased after introduction of pDeltaE1-p53. The telomerase activity and the transcriptional activity of hTERT promoter were inhibited. The cells cycles of transfected SACC-83 were arrested in G(1) phase and the rate of colony-formation was decreased, and similarly the tumorigenicity in nude mice was also decreased.</p><p><b>CONCLUSIONS</b>The introduction of wild-type p53 by adenoviral vector could suppress the telomerase activity and malignant phenotypes of salivary adenoid cystic carcinoma cells.</p>


Subject(s)
Animals , Male , Mice , Carcinoma, Adenoid Cystic , Genetics , Metabolism , Pathology , Cell Line, Tumor , Genetic Vectors , Mice, Inbred BALB C , Mice, Nude , Salivary Gland Neoplasms , Genetics , Metabolism , Pathology , Telomerase , Genetics , Metabolism , Transfection , Tumor Suppressor Protein p53 , Genetics
13.
Chinese Journal of Stomatology ; (12): 297-298, 2006.
Article in Chinese | WPRIM | ID: wpr-354392

ABSTRACT

<p><b>OBJECTIVE</b>To determine the correlation between methylation of p16 gene in promoter region and the carcinogenesis and progression of squamous cell carcinoma (SCC) of buccal mucosa.</p><p><b>METHODS</b>Methylation of pl6 gene in SCC and leukoplakia of buccal mucosa was investigated by MSP and pl6 protein was analyzed by Western blot.</p><p><b>RESULTS</b>The methylation of p16 gene was found in 15 of 30 cases SCC and 1 of 10 cases of leukoplakia of buccal mucosa (P < 0.05). Methylation of p16 gene in SCC of buccal mucosa was not related with age, sex, cell differentiation and clinical stage. But methylation of p16 in the cases with lymph node-metastasis was higher than that in the cases without lymph node-metastasis protein (P < 0.05). Meanwhile Methylation of p16 gene was positively correlated with no-expression of p16 protein (P < 0.01).</p><p><b>CONCLUSIONS</b>The methylation of p16 gene leaded to the inactivation of p16 gene and was related with the carcinogenesis and progress of SCC of buccal mucosa.</p>


Subject(s)
Humans , Carcinoma, Squamous Cell , Genetics , Metabolism , Pathology , Cheek , Cyclin-Dependent Kinase Inhibitor p16 , Genetics , Metabolism , DNA Methylation , Genes, p16 , Leukoplakia, Oral , Embryology , Genetics , Pathology , Mouth Neoplasms , Genetics , Metabolism , Pathology , Promoter Regions, Genetic
14.
West China Journal of Stomatology ; (6): 362-365, 2006.
Article in Chinese | WPRIM | ID: wpr-288927

ABSTRACT

<p><b>OBJECTIVE</b>To explore the correlation between homozygous deletions and mutation of p16 gene and the carcinogenesis and progression of squamous cell carcinoma of buccal mucosa.</p><p><b>METHODS</b>Thirty buccal cancers, 10 leukoplakias and 8 buccal mucosas were involved. DNA was extracted from the tissues. PCR was used to analyses homozygous deletion of p16 gene. PCR-SSCP-DNA sequencing was performed to detect the point mutation of p16 gene. Immunohistochemical techniques were used to detect the expression of P16 protein.</p><p><b>RESULTS</b>Gene deletions and point mutations were not found in leukoplakia and normal buccal mucosa. Gene deletions were found in 7 samples out of 30 cases of squamous cell carcinoma of buccal mucosa (23.3%), while point mutations were found in 5 samples out of 30 cases of squamous cell carcinoma of buccal mucosa (16.7%). Sequencing analysis showed that 5 cases point mutations were missense mutations, occurred on exon 2. Three cases occurred in the same point, codon 99 (GAT --> AAT). The result of immunohistochemical stains showed that 11 out of 12 cases gene inactivation did not expressed P16 protein.</p><p><b>CONCLUSION</b>Homozygous deletion and point mutation of p16 were the main pattern of gene inactivation in squamous cell carcinoma of buccal mucosa. There was a closely correlation between p16 gene inactivation and the carcinogenesis of squamous cell carcinoma of buccal mucosa.</p>


Subject(s)
Humans , Carcinoma, Squamous Cell , Cyclin-Dependent Kinase Inhibitor p16 , Gene Deletion , Genes, p16 , Mouth Mucosa , Mutation , Point Mutation
15.
West China Journal of Stomatology ; (6): 65-68, 2005.
Article in Chinese | WPRIM | ID: wpr-329983

ABSTRACT

<p><b>OBJECTIVE</b>To study the therapeutic effects of combined gene therapy of wild type p53 (wt-p53) and herpes simplex virus thymidine kinase (HSV-tk) gene on pleomorphic adenoma cells of salivary gland.</p><p><b>METHODS</b>Wild type p53 and HSV-tk gene were transfected into human pleomorphic adenoma cells of salivary gland by using recombinant adenovirus vector. The efficiency of transfection was checked and gene was expressed by RT-PCR methods. The cell inhibition after transfected was verified by light microscope and MTT.</p><p><b>RESULTS</b>The proliferation of the pleomorphic adenoma cells transfected wt-p53 and HSV-tk gene was inhibited and the cell survival rate decreased to 54% and 38% respectively in 5 days. However, when wt-p53 gene combined with HSV-tk/GCV system, the killing effects was significantly stronger (P < 0.05) and the cell survival rate decreased to 20%.</p><p><b>CONCLUSION</b>Combining p53 gene with HSV-tk/GCV system for gene therapy in pleomorphic adenoma cells of salivary gland is a valuable method.</p>


Subject(s)
Humans , Adenoma, Pleomorphic , Antiviral Agents , Cell Line, Tumor , Cell Survival , Ganciclovir , Genes, p53 , Genetic Therapy , Genetic Vectors , Salivary Glands , Simplexvirus , Thymidine Kinase , Transfection
16.
West China Journal of Stomatology ; (6): 295-298, 2005.
Article in Chinese | WPRIM | ID: wpr-300311

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the effectiveness of early treatment with the Twin-block appliance for the developing Class II division 1 malocclusion.</p><p><b>METHODS</b>A Total of 30 children with Class II division 1 malocclusion, 18 (8 male, 10 female) out of which received treatment with the Twin-block appliance, the other 12 cases (6 male, 6 female) without treatment served as control group. Cephalometric data were collected at the start and the end of the study and statistical analysis were applied.</p><p><b>RESULTS</b>Except the factor of growth, treatment with the Twin-block appliance resulted in reduction of ANB (1.55 degrees), overjet (5.46 mm) and correction of molar relationship (4.07 mm). These changes were due to the change of Pg/OLp, Co/OLp and mandibular length. The change of A/OLp was not significant. The skeletal effect contributing to the change on overjet and molar relation were 58% and 78% respectively.</p><p><b>CONCLUSION</b>Early treatment with the Twin-block appliance was effective in reducing ANB angle, overjet and correction of molar relationship. The changes were mainly profit from the favorable skeletal change of mandible, especially from its length, while the effect on maxillary was not significant.</p>


Subject(s)
Child , Female , Humans , Male , Cephalometry , Malocclusion, Angle Class II , Mandible , Maxilla , Molar , Orthodontic Appliances, Functional , Treatment Outcome
17.
Chinese Journal of Plastic Surgery ; (6): 380-383, 2004.
Article in Chinese | WPRIM | ID: wpr-255140

ABSTRACT

<p><b>OBJECTIVE</b>To observe the effect of an external film of hyaluronic acid (HA) on the rats wound healing.</p><p><b>METHODS</b>Forty-eight SD rats were randomly separated into eight groups of 6 rats each. Bilateral dorsal cuts were performed on each rat, left wound was used as the experiment with HA external film and right wound was used as the control only with normal saline. The process of healing was observed histologically following 1st, 3rd, 5th, 7th, 9th, 14th, 21st, and 28th days postoperatively.</p><p><b>RESULTS</b>Inflammation was lighter and epidermal healing was faster in the experimental group than those in the control. The fibroblasts degenerated and the collagen fiber changed to slim and loose bunches in the experimental group.</p><p><b>CONCLUSION</b>The results indicated that HA external film could have powerful infiltrating activity at the early stage of wound healing, it could accelerate the healing of epidermis and delay the formation of keratinization layer.</p>


Subject(s)
Animals , Male , Rats , Collagen , Metabolism , Drug Administration Routes , Fibroblasts , Metabolism , Hyaluronic Acid , Pharmacology , Random Allocation , Rats, Sprague-Dawley , Treatment Outcome , Wound Healing
18.
West China Journal of Stomatology ; (6): 309-311, 2004.
Article in Chinese | WPRIM | ID: wpr-330059

ABSTRACT

<p><b>OBJECTIVE</b>To determine the level of hyaluronic acid (HA) in serum of patients with oral and maxillofacial malignancy and to investigate the correlation between the levels of serum HA and stage of the malignant lesions and treatment response.</p><p><b>METHODS</b>44 patients with oral and maxillofacial malignancy were analyzed and 24 healthy individuals served as controls. Venous blood was collected from the patients before treatment and the healthy individuals. One week after therapy, venous blood were collected in 24 patients once again. Serum levels of HA were measured with quantitative radioimmunoassay (RIA).</p><p><b>RESULTS</b>Before treatment, the serum HA concentration in patients with oral and maxillofacial malignancy was significantly higher than that of the controls (P < 0.05). Also, the serum HA concentration in patients with OSCC was significantly higher than that of the controls (P < 0.05). No difference was noted in serum HA concentration between patients with salivary ACC and the control group (P > 0.05). The serum HA concentration of patients in stage III and IV was significantly higher than that of patients in stage I and II (P < 0.05). Serum HA levels decreased in patients after a complete treatment, but the difference was not significant (P > 0.05).</p><p><b>CONCLUSION</b>Serum levels of HA may be useful in diagnosis of OSCC and was associated with clinical stages in patients with oral and maxillofacial malignancy. However, it may not be contributory to monitoring treatment response in patients with oral and maxillofacial malignancy.</p>


Subject(s)
Humans , Case-Control Studies , Hyaluronic Acid , Blood , Mouth Neoplasms , Blood , Neoplasm Staging
19.
Chinese Journal of Stomatology ; (12): 358-360, 2003.
Article in Chinese | WPRIM | ID: wpr-253698

ABSTRACT

<p><b>OBJECTIVE</b>To study the feature of apoptosis of salivary adenoid cystic carcinoma (SACC) induced by recombined human tumor necrosis factor-alpha (rhTNF-alpha) in nude mice, and to evaluate the related genes expression of apoptosis.</p><p><b>METHODS</b>Twelve SPF grade 4 approximately 5 weeks old female Balb/c nude mice were selected in this study. SACC-83 cells were collected to 6 x 10(7) per milliliter and injected subcutaneously. Group A and B were experimental group which was given 100 x 10(4) IU/kg TNF-alpha or 10 x 10(4) IU/kg TNF-alpha respectively. Group C was only given normal saline and used as normal control. The investigations were adopted by using both light and transmission electron microscope (LM and TEM), flow cytometer and In Situ Cell Death Detection Kit. The evaluations of bax and bcl-2 expression were utilized by immunohistochemistry.</p><p><b>RESULTS</b>The percentage of apoptosis of transplanted tumors was much higher than that of the control (P<0.01). Apoptotic cells were calcified and grit bodies were formed. Apoptotic cells expressed and contained significantly higher proportions of both bax and bcl-2 proteins (P<0.05).</p><p><b>CONCLUSIONS</b>It is suggested that calcification may be the obvious feature and the last outcome of the apoptosis of SACC transplanted tumors. Apoptosis induced by TNF-alpha can increase the expressions of bax and bcl-2.</p>


Subject(s)
Animals , Female , Mice , Apoptosis , Carcinoma, Adenoid Cystic , Chemistry , Pathology , Therapeutics , Mice, Inbred BALB C , Mice, Nude , Proto-Oncogene Proteins , Proto-Oncogene Proteins c-bcl-2 , Salivary Gland Neoplasms , Chemistry , Pathology , Therapeutics , Tumor Necrosis Factor-alpha , Pharmacology , bcl-2-Associated X Protein
20.
Chinese Journal of Rehabilitation Theory and Practice ; (12): 162-163, 2002.
Article in Chinese | WPRIM | ID: wpr-980452

ABSTRACT

@#ObjectiveTo observe the rehabilitative effect of patients with shoulder-hand syndrome after stroke by manipulation treatment. MethodsThe patients with shoulder-hand syndrome were randomly divided into two groups, manipulation group (180cases) and control group (128 cases). Patients in the manipulation group were regularly given a passive quantitative movement on shoulder, elbow and hand joints,while patients in the control group were irregularly given a passive movement or ordered to perform an autonomic movement. The signs and symptoms of patients in these two groups were not much different. The rehabilitative effects were compared 3 months later. ResultsSigns and symptoms in the manipulation groups improved much better than that of the control group. Conclusions The manipulation treatment for the post-stroke patients with shoulder-hand syndrome is the method that is simple, effective and easy to perform.

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