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1.
West China Journal of Stomatology ; (6): 253-263, 2011.
Article in Chinese | WPRIM | ID: wpr-235073

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the drug distribution in tissues of cervical lymph node metastasis mice model after submucosa adjacent cancer injection of pingyangmycin-activated carbon nanoparticles (PYM-CH-NP) and evaluate the lymph targeting effect of PYM-CH-NP.</p><p><b>METHODS</b>Pingyangmycin (PYM) was radiolabeled with 125I by modified the chloramine T method. Cervical lymph node metastasis mice model was established by buccal submucosa inoculation of a high lymph metastasis cell line U14 cancer cell. 360 mice models burdened with cervical lymph metastasis were randomly divided into 3 groups. PYM group was treated with PYM water solution, PYM-CH-NP group was treated with PYM-CH-NP. Negative control group was injected with activated carbon nanoparticles. PYM-CH-NP and pingyangmycin water solution were injected in pericancer submucosa of the mice respectively. The radioactivity of drug in blood, heart, liver, spleen, lung, kidney and cervical lymph node were measured after 0.5, 1, 4, 8, 12, 24, 48, 72, 96, 120, 144, 168 h administration. The radioactivity of each samples per unit weight were calculated. The selectivity index (SI) and targeting index (TI) of drug were calculated.</p><p><b>RESULTS</b>The radioactivity of drug in cervical lymph node of PYM-CH-NP group was much higher than PYM group in each time point (P < 0.001), whereas the blood, heart, liver, spleen, lung and kidney uptake of pingyangmycin was greatly decreased in PYM-CH-NP group after 4 h administration (P < 0.001). The SI value of PYM group at each time point was less than 1. While the minimum SI and TI value of PYM-CH-NP was 1.793 and 1.562, the maximum value reached to 68.126 and 14.623 after 72 h administration.</p><p><b>CONCLUSION</b>PYM-CH-NP can increase drug dosage in metastasized cervical lymph nodes, and decrease drug dosage of other organs. So better therapeutic outcome and little adverse reaction may be achieved for lymph node metastasis.</p>


Subject(s)
Animals , Mice , Bleomycin , Carbon , Lymph Nodes , Lymphatic Metastasis , Mouth Neoplasms , Nanoparticles , Neck
2.
Chinese Medical Journal ; (24): 2803-2806, 2010.
Article in English | WPRIM | ID: wpr-237412

ABSTRACT

<p><b>BACKGROUND</b>Median sternotomy is considered the most usually performed procedure in cardiac operations. This study aimed to assess clinical effectiveness of bilateral pectoralis major muscle flaps (BPMMF) for management of sternal osteomyelitis and mediastinal infection following median sternotomy.</p><p><b>METHODS</b>Clinical data were collected and retrospectively analyzed from twelve patients who underwent the BPMMF transposition for management of sternal osteomyelitis and mediastinal infection following median sternotomy from January 2006 to June 2009. Procedure consisted of rigorous debridement of necrotic tissues, dead space obliteration using the BPMMF, and placement of drainage tubes connected to a negative pressures generator for adequate drainage.</p><p><b>RESULTS</b>No patients died of drainage, and all 12 patients had viable BPMMF when discharged from hospital. At 1 week post discharge, 2 patients presented with sternal infection but recovered following local debridement and medication. No patients showed infection recurrence during the follow-up period over 10 months.</p><p><b>CONCLUSIONS</b>Sternal osteomyelitis and mediastinal infection following median sternotomy may be effectively managed through rigorous debridement of infected soft tissues, resection of the damaged sternal segment, transposition of the BPMMF to fill the damaged sternum resulting from debridement, and adequate postoperative drainage.</p>


Subject(s)
Adolescent , Adult , Aged , Humans , Male , Middle Aged , Debridement , Follow-Up Studies , Mediastinitis , General Surgery , Osteomyelitis , General Surgery , Retrospective Studies , Sternotomy , Sternum , General Surgery , Surgical Flaps , Surgical Wound Infection , General Surgery
3.
West China Journal of Stomatology ; (6): 257-260, 2010.
Article in Chinese | WPRIM | ID: wpr-246609

ABSTRACT

<p><b>OBJECTIVE</b>The cytotoxic effects of a new formulation of Pingyangmycin-activated carbon nanoparticles (PYM-CH-NP) on two human oral squamous cell carcinoma Tca8113 and BcaCD885 cell lines were studied in vitro.</p><p><b>METHODS</b>The inhibitory effects of PYM-CH-NP and Pingyangmycin (PYM) were evaluated by methyl thiazolyl tetrazolium (MTT) assay at 1-7 days. The 50% inhibition concentration values (IC50) and relative antitumor activity (RAA) of PYM-CH-NP and PYM against Tca8113 and BcaCD885 with different drug concentration were evaluated. The time-dependent cytotoxic effects of PYM-CH-NP and PYM were during 1-5 days, so the doseeffect relationship was investigated at 5th day.</p><p><b>RESULTS</b>Both PYM-CH-NP and PYM had high anticancer effects on Tca8113 and BcaCD885, and the cytotoxic effects were dose-dependent and time-dependent.</p><p><b>CONCLUSION</b>The activated carbon nanoparticles (CH-NP) may serve as a new drug delivery carrier of PYM. The new formulation PYM-CH-NP could slow down drug release, prolonged the drug concentration and its acting time, so more effective anticancer efficacy could be achieved.</p>


Subject(s)
Humans , Antibiotics, Antineoplastic , Bleomycin , Carbon , Carcinoma, Squamous Cell , Cell Line , Cell Line, Tumor , In Vitro Techniques , Mouth Neoplasms , Nanoparticles
4.
Chinese Medical Journal ; (24): 1875-1881, 2008.
Article in English | WPRIM | ID: wpr-350804

ABSTRACT

<p><b>BACKGROUND</b>Researchers have recently demonstrated that thrombospondin-1 (TSP-1) has an important function in regulating neovascularization. Whether it inhibits or accelerates neovascularization, however, is still controversial. We found few reports about the correlation between TSP-1 and vascularization in mucoepidermoid carcinoma. In this research, the distribution and expression of TSP-1 in mucoepidermoid carcinoma were investigated. We also analyzed (1) the correlation between the expression of TSP-1 and microvessel density (MVD), as an indicator of neovascularization activity, and (2) the effect of TSP-1 on neovascularization and tumor growth in the subcutaneous xenotransplanted model of mucoepidermoid carcinoma.</p><p><b>METHOD</b>(1) The sites and intensity of expression of TSP-1 and the MVD were analyzed in 45 cases of mucoepidermoid carcinoma after surgery by the method of streptavidin-peroxidase (SP) immunohistochemistry; and (2) recombinant human thrombospondin-1 (rhTSP-1) was injected twice a week for five consecutive weeks around the tumor in the subcutaneous xenotransplanted tumor model of mucoepidermoid carcinoma in nude mice. Each week, the tumor size was measured, in order to draw the growth curve of the xenotransplanted tumor model of mucoepidermoid carcinoma, and MVD was measured.</p><p><b>RESULTS</b>(1) The positive expression of TSP-1 protein was 57.78% (26/45). Most positive staining for TSP-1 was found in the cytoplasm of the cancer cells, while some staining occurred in the extracellular matrix. The mean MVD in 45 cases of mucoepidermoid carcinoma was 58.17 +/- 19.77 per 100 visual fields. Tumors with a high expression of TSP-1 showed a low MVD value, and the TSP-1 immunocompetence and microvessel density showed a significant negative correlation (r(s) = -0.947, P < 0.001). (2) The xenotransplanted tumors with the injection doses of 1.25, 0.75 and 0.25 microg/ml respectively were 36.97%, 53.36% and 73.61% of the size of the control group ((451 +/- 92), (651 +/- 113), (898 +/- 86) and (1220 +/- 157) mm(3) respectively, F = 53.167, P < 0.001), and their weights were respectively 35.14%, 51.35% and 70.27% of the control group ((1.3 +/- 0.5), (1.9 +/- 0.5), (2.6 +/- 0.3), and (3.7 +/- 0.7) g respectively, F = 62.669, P < 0.001). Their MVDs were 25.00%, 45.93%, and 72.20% respectively of the control group and concentration dependent (15.43 +/- 3.45, 28.35 +/- 4.24, 44.57 +/- 3.35 and 61.73 +/- 5.43 per 100 visual fields respectively, F = 54.582, P < 0.001).</p><p><b>CONCLUSIONS</b>The TSP-1 has a higher expression in mucoepidermoid carcinoma and the expression has a significant negative correlation with neovascularization. The TSP-1 inhibits neovascularization and tumor growth, and it might be a new biological therapy for treatment of patients with mucoepidermoid carcinoma.</p>


Subject(s)
Adult , Aged , Animals , Female , Humans , Male , Mice , Middle Aged , Carcinoma, Mucoepidermoid , Chemistry , Pathology , Neoplasm Transplantation , Neovascularization, Pathologic , Pathology , Recombinant Proteins , Pharmacology , Thrombospondin 1 , Pharmacology , Transplantation, Heterologous
5.
West China Journal of Stomatology ; (6): 475-478, 2008.
Article in Chinese | WPRIM | ID: wpr-264384

ABSTRACT

<p><b>OBJECTIVE</b>To study the mechanism of sensitivity variation to cisplatin caused by nm23-H1.</p><p><b>METHODS</b>The samles was divided into two groups: Tca8113 group and Tca8113/nm23-H1 group. Using MTT and flow cytometer, the changes of cell mortality rate, apoptosis and mitochondrial membrane potential were detected. By VG PQ Excell, the changes of the intracellular platinum were detected.</p><p><b>RESULTS</b>In vitro the cell mortality rate and apoptosis were increased in Tca8113/nm23-H1 group, comparing with Tea8113 group. Mitochondrial membrane potential was decreased in Tca8113/nm23-H1 group. The intracellular platinum was increased significantly in Tca8113/nm23-H1 group. This effect could be inhibited by oubain which was an inhibitor of Na+/K+-ATP.</p><p><b>CONCLUSION</b>nm23-H1 can increase the sensitivity of cisplatin on Tca8113 cell line. The mitochondrial membrane potential was decreased by nm23-H1 so that intracellular platinum was increased and finally increased the apoptosis or necrosis.</p>


Subject(s)
Humans , Apoptosis , Cell Line , Cell Line, Tumor , Cisplatin , In Vitro Techniques , NM23 Nucleoside Diphosphate Kinases , Transfection
6.
West China Journal of Stomatology ; (6): 500-503, 2007.
Article in Chinese | WPRIM | ID: wpr-348008

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the differently expressed Homeobox genes between lingual squmaous cell carcinoma and normal mucosa.</p><p><b>METHODS</b>Seven paired specimens including lingual squmaous cell carcinoma and its surrounding normal tissue were obtained from 7 patients. Customized Oligo microarray which contains numerous probes of 232 human Homeobox genes was used to analyse the results. All datas were scanned by Agilent scanner and differentiately expressed genes were sorted out.</p><p><b>RESULTS</b>Homeobox gene NANOG was found up-regulated in 5 samples. PHTF2 was found down-regulated in 7 samples, and CRX, PITX1, OTEX was found down-regulated in 5 samples.</p><p><b>CONCLUSION</b>As the key gene to cellular proliferation and differentiation, Homeobox genes is closely releverant to the oncogenesis of lingual squmaous cell carcinoma.</p>


Subject(s)
Humans , Cell Differentiation , Gene Expression Regulation, Neoplastic , Genes, Homeobox , Mucous Membrane
7.
West China Journal of Stomatology ; (6): 508-512, 2007.
Article in Chinese | WPRIM | ID: wpr-348006

ABSTRACT

<p><b>OBJECTIVE</b>To approach the effects on induction of differentiation of Tca8113 cells affected by abscisic acid.</p><p><b>METHODS</b>The changes of surface differentiation markers, cell configuration, restrain of cell growth and the expression of Caspase-3 mRNA were examined by using inverted-phase contrast microscope, immunohistochemistry (IHC) and in situ hybridization in vitro. The dependablity between the surface differentiation markers and Caspase-3 mRNA was analysed.</p><p><b>RESULTS</b>The restraint of cell growth in ABA groups was higher than that of the control group (P<0.05). There was a trend that the tumor cell had transformed the normal cell. Furthermore, the time-dosage dependent relationship existed in the inhibition rate of tumor cells. The results showed that the expressions of Involucrin protein, retinoic acid receptor beta (RARbeta) and Caspase-3 mRNA in experimental group had been higher than that of control group. There was a significance between the different concentration experimental groups at 24 h (P<0.05). Moreover, the positive correlation existed among the Involucrin, RARbeta and Caspase-3 mRNA at the time of 12 hour and 24 hour (P<0.05).</p><p><b>CONCLUSION</b>The possible mechanism is that abscisic acid acted on the tumor cell and raised the level of RARbeta gene through combining the correlative receptors so that increased the expression of Involucrin protein and promoted the activity of Caspase-3 and resulted in apoptosis of tumor cell.</p>


Subject(s)
Abscisic Acid , Apoptosis , Cell Differentiation , Cell Division , Cell Proliferation , In Vitro Techniques , RNA, Messenger , Receptors, Retinoic Acid
8.
Chinese Journal of Stomatology ; (12): 284-287, 2007.
Article in Chinese | WPRIM | ID: wpr-333342

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the evidences of the presence of tumor stem cells and its impact on the tumorigenesis of adenoid cystic carcinoma cell (ACC)-2 cell line by analyzing the biologic characteristics of different sub-clones of adenoid cystic carcinoma cell line.</p><p><b>METHODS</b>In vitro individual cell culture was employed to observe the proliferating character of ACC-2 cells. The expression of CD44(+) and CD24(-) of ACC-2 cells were investigated by immunohistochemical. Immunomagnetic isolation of different phenotype of ACC-2 cells, followed by cell culture, was used to study the proliferating abilities of different clusters of the cell line. The hetero-transplanted tumor mold was established using BALB/C nude mice by subcutaneous injection of tumor cells. The tumorigenic and differentiating properties of the different cluster were investigated.</p><p><b>RESULTS</b>Only 4.41% of cultured ACC-2 cell had ability of division, proliferation and establishment of cell clone. CD44(+)-CD24(-) cluster accounted for about 8.1% of total ACC-2 cells, among which, 25.71% cells could divide and proliferate. All of CD44 and CD44(+)-CD24(+) cells were failure to be eternal alive in the condition of in vitro individual cell culture. According to the results of in vivo tumorigenic study, the minimal cell quantity to develop a subcutaneous transplanted tumor by CD44(+)-CD24(-) cells was 1 x 10(3), where as the needed cell amount were 1 x 10(5) and 1 x 10(4) as to non-isolated ACC-2 cells and CD44(+) cells, respectively. The CD44(-) and CD44(+)-CD24(+) did not develop transplanted tumors. CD44(+)-CD24(-) ACC-2 cell could differentiate into cells of other phenotypes.</p><p><b>CONCLUSIONS</b>CD44(+)-CD24(-) ACC-2 cells consist of a very small portion of all ACC-2 cells (about 4%). They have remarkable proliferating ability and can bear special phenotypes, The tumorogenic ability of CD44(+)-CD24(-) cells are stronger than that of CD44(+) and non-isolated ACC-2 cells. Eliminating of this cluster from ACC-2 would actually deprive the tumorogenic ability of the cell line.</p>


Subject(s)
Animals , Humans , Mice , Carcinoma, Adenoid Cystic , Pathology , Cell Differentiation , Cell Line, Tumor , Cell Proliferation , Mice, Inbred BALB C , Mice, Nude , Mouth Neoplasms , Pathology , Neoplastic Stem Cells , Pathology , Xenograft Model Antitumor Assays
9.
West China Journal of Stomatology ; (6): 64-66, 2007.
Article in Chinese | WPRIM | ID: wpr-249754

ABSTRACT

<p><b>OBJECTIVE</b>To assess the clinical and histological features and therapeutic efficacy of 30 cases of malignant sublingual salivary gland tumors.</p><p><b>METHODS</b>The clinicopathologic data of 30 patients with malignant sublingual salivary gland tumor were obtained from West China Hospital of Stomatology, Sichuan University from 1955 to 2005.</p><p><b>RESULTS</b>There were 18 male and 12 female, and the average age of patients was 50.6 years old. Seventeen cases were adenoid cystic carcinoma, accounting for 56.7%. There were 17 cases clinically staged as III, accounting for 56.7%. Distant metastasis and tumor recurrence were the main death reasons. The overall local recurrence rate was 30.0%, and distant metastasis rate was 26.7%.</p><p><b>CONCLUSION</b>Sublingual gland malignant tumors are rare and most of them are adenoid cystic carcinoma. Surgery is the main treatment option. The resection of the tumor accompanying with the neck dissection is the key method to achieve good therapeutic effect. The postoperative radiotherapy and chemotherapy should be adjuvant.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Carcinoma, Adenoid Cystic , China , Retrospective Studies , Salivary Gland Neoplasms , Sublingual Gland
10.
Chinese Journal of Stomatology ; (12): 550-552, 2007.
Article in Chinese | WPRIM | ID: wpr-359698

ABSTRACT

<p><b>OBJECTIVE</b>To search for specific serum biomarkers associated with tongue cancer by means of the serum proteomics technology.</p><p><b>METHODS</b>The tongue cancer cells of human tongue cancer cell line Tca8113 were subcutaneously inoculated into nude mice, while control nude mice were injected with phosphate-buffered saline. Serums from these two group of mice were collected for proteomic analysis using two-dimensional gel electrophoresis (2-DE) and mass spectrometry (MS).</p><p><b>RESULTS</b>Comparing the serum 2-DE maps from the tumor-bearing mice with those produced from control mice, we found that squamous cell carcinoma antigen 1 was over expressed only in the serum of tumor-bearing mice.</p><p><b>CONCLUSIONS</b>The squamous cell carcinoma antigen 1 may be of great potential as the biomarker of tongue cancer and as the potential therapeutic target for gene therapy.</p>


Subject(s)
Animals , Humans , Mice , Biomarkers, Tumor , Blood , Carcinoma, Squamous Cell , Blood , Pathology , Cell Line, Tumor , Electrophoresis, Gel, Two-Dimensional , Mass Spectrometry , Mice, Inbred BALB C , Mice, Nude , Proteomics , Methods , Tongue Neoplasms , Blood , Pathology , Xenograft Model Antitumor Assays
11.
West China Journal of Stomatology ; (6): 170-172, 2006.
Article in Chinese | WPRIM | ID: wpr-288975

ABSTRACT

<p><b>OBJECTIVE</b>To study the effect of protein-cisplatin and nm23-H1 therapy on the tumor of nude mouse.</p><p><b>METHODS</b>The 15 BALB/C female mice were divided into three groups, control group, protein-cisplatin group and protein-cisplatin+nm23-H1 plasmid group. Tca8113 were injected into the mice subcutaneously with the concentration of 3.1 x 10(6) cells/mL. After two weeks, the mixture of lipofectin and nm23-H1 was injected around xenograft of nude mouse. After three days, the protein-cisplatin was injected around xenograft. The weight of mouse, the volume and the weight of xenograft were measured.</p><p><b>RESULTS</b>The weight of mouse was lightest in control group. The volume and weight of the transplanted tumor were lightest in nm23-H1 +protein-cisplatin group.</p><p><b>CONCLUSION</b>The combination therapy of nm23-H1 and protein-cisplatin can effectively inhibites the growth of xenograft in nude mouse.</p>


Subject(s)
Animals , Female , Mice , Cisplatin , Heterografts , Mice, Inbred BALB C , Mice, Nude , NM23 Nucleoside Diphosphate Kinases , Neoplasm Transplantation , Transfection
12.
West China Journal of Stomatology ; (6): 357-361, 2006.
Article in Chinese | WPRIM | ID: wpr-288928

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the ectopic osteogenesis potential of human natural bone derived material combined with human bone marrow mesenchymal stem cells (MSCs).</p><p><b>METHODS</b>Cell-scaffold complexes were implanted subcutaneously into the left back of the nude mice, and human natural bone derived material were implanted into the right back as control group. The mice were killed respectively on the postoperative 2 weeks, 4 weeks and 8 weeks. The macroscopic, histopathological, alkaline phosphatase (ALP) activity assay methods were performed to assess the ectopic osteogenesis potential.</p><p><b>RESULTS</b>The cartilaginous osteogenesis were observed in both deproteinated bone and decalcified bone, and the more new bone tissue formed gradually as the time went by after implantation. ALP activity become stronger followed with the time (P < 0.05), and compared with the decalcified bone, deproteinated bone displayed stronger ALP activity (P < 0.05).</p><p><b>CONCLUSION</b>The MSCs and human natural bone derived material can be used as good seed cells and scaffold materials respectively to construct tissue-engineered bone, and as the scaffold material, deproteinated bone has better osteogenesis ability than decalcifed bone.</p>


Subject(s)
Animals , Humans , Mice , Bone and Bones , Cells, Cultured , Mesenchymal Stem Cells , Mice, Nude , Osteogenesis , Tissue Engineering
13.
West China Journal of Stomatology ; (6): 49-52, 2005.
Article in Chinese | WPRIM | ID: wpr-329988

ABSTRACT

<p><b>OBJECTIVE</b>The relationship between the mode of tumor invasion in the tumor-host borderline and the frequency of cervical lymph node metastasis was investigated in squamous cell carcinoma of the oral cavity.</p><p><b>METHODS</b>200 cases with histologically proven squamous cell carcinoma of the oral cavity were studied by histological method with HE stained. The mode of invasion in the tumor-host relationship was classified into five grades by Yamamoto's criteria.</p><p><b>RESULTS</b>With regard to the relationship between the mode of invasion and metastasis, the more invasive the tumor tissue was, the more frequent the metastasis formed (P < 0.001). The frequency of metastasis in grades 1 and 2 was low (0 and 5.9%, respectively), The frequency of metastasis in grades 3 was moderate (14.3%), and that in grades 4c and 4d was highly rapid (63.0% and 82.9%, respectively). Single node metastases were frequent in grade 3 and grade 4c (66.7% and 58.8%, respectively), while plural node metastases were frequent in grade 4d (70.6%, P < 0.05). Moreover, the distribution of metastasized lymph nodes was focused on level 1 (41.2%) or level 1 and 2 (79.4%) in grade 4c and was dispersed from level 1 to 4 in grade 4d (P < 0.05). In the present study, the degree of differentiation did not correlate well with the frequency of metastasis.</p><p><b>CONCLUSION</b>These results indicate that the more invasive the tumor cells were to the host, the more frequent the metastasis formed. The different mode of invasion would accompany with different frequency of metastasis, different number and distribution of metastasized lymph nodes.</p>


Subject(s)
Aged , Female , Humans , Middle Aged , Carcinoma, Squamous Cell , Cell Differentiation , Lymph Nodes , Lymphatic Metastasis , Mouth Neoplasms , Neck , Neoplasm Invasiveness
14.
West China Journal of Stomatology ; (6): 69-71, 2005.
Article in Chinese | WPRIM | ID: wpr-329982

ABSTRACT

<p><b>OBJECTIVE</b>The aim of this study was to prepare Pingyangmycin Albumin Microspheres (PYM-AMS) for arteriovenous malformations treatment.</p><p><b>METHODS</b>PYM-AMS was prepared at 140 degrees C by the method of emulsification-heat solidification and its characteristics were evaluated, such as morphosis, particle size, drug loading (DL%), encapsulation efficiency (EE%), stability and drug sustained-releasing in vitro. After being packaged, PYM-AMS were sterilized with 13.7 kGy of 60Co. Small samples of PYM-AMS were packaged in small bottles and stored at 3 - 5 degrees C, 15 - 25 degrees C, 37 degrees C for 3 months, then checked the change of morphology, DL, EE and the release rate.</p><p><b>RESULTS</b>The surface of particles was smooth and integrated. The average diameter of PYM-AMS particles was 139.422 microm and 80% was in the range of 56 - 251 microm. The mean DL% and EE% were 26.47% and 84.3%, respectively. PYM released fast in 5 h, but then released slowly. 88.65% drugs were released in 24 h, and t50 was 1.5 h. There was no obvious change of the morphology, DL,EE and the release rate of PYM-AMS stored at 3 - 5 degrees C 15 - 25 degrees C, 37 degrees C for 3 months.</p><p><b>CONCLUSION</b>PYM-AMS prepared in this study had sustained-release effect, high drug loading and high stability. Albumin is a good carrier of PYM embolization agent.</p>


Subject(s)
Albumins , Bleomycin , Delayed-Action Preparations , Microspheres , Particle Size
15.
West China Journal of Stomatology ; (6): 128-135, 2005.
Article in Chinese | WPRIM | ID: wpr-329968

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the microbial contents presented on the surface of mucosa in the oral cavity of patients who accepted radiotherapy, and to provide the evidences of controlling post-radiotherapeutic infections.</p><p><b>METHODS</b>32 patients (19 males and 13 females) aged from 37 - 72 received radiotherapy after oral squamous cell carcinomas operation were selected. Samples of saliva were obtained from the radiated center and opposite mucosa before and after radiotherapy. The detective amount, detective ratio and constituent ratio were analysed by cultivation and identification.</p><p><b>RESULTS</b>Streptococci, Candida albicans and Pseudomonas aeruginosa significantly increased on both sides of the oral mucosa while Neisseria and Actinobacillus decreased on radiated region after the radiotherapy.</p><p><b>CONCLUSION</b>Radiotherapy has great effects on oral bacteria and pathogenic organism may play a role in post-radiotherapy infections. It is necessary to do bacteria culture and choose sensitive antibiotics regularly for post-radiotherapeutic patients.</p>


Subject(s)
Humans , Anti-Bacterial Agents , Bacteria , Candida albicans , Carcinoma, Squamous Cell , Microbiology , Radiotherapy , Mouth Mucosa , Microbiology , Mouth Neoplasms , Microbiology , Radiotherapy , Postoperative Period , Saliva
16.
West China Journal of Stomatology ; (6): 471-473, 2005.
Article in Chinese | WPRIM | ID: wpr-300269

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the feasibility of plasmid nm23-h1 transfection on high metastatic potential adnoid cystic carcinoma (ACC-M) cell line mediated by cationic lipid.</p><p><b>METHODS</b>ACC-M cell were implanted in the maxillofacial region in each of 40 BALB/c nude mice. After the tumor growth to 1 cm in diameter, 0.1 ml Lipofctamine-nm23-hl plasmid complex were injected intratumorally in 10 mice, 3 days after the first injection, 10 mices injected for twice, 10 mice as plamid-blank control, another 10 mice were injected 0.2 ml complex, 2, 3, 7days after the injection, the mice were killed and the specimen for HE and immunohistological chemistry study.</p><p><b>RESULTS</b>nm23-h1 expression initiated in the tumor cells 3 days after the complex injection, 7 days later, the expression level increased accompanying with extracellular matrix increase, twice injection and multiple channel injection would gain better nm23-h1 expression than once injection and single-channel injection respectively.</p><p><b>CONCLUSION</b>Cationic lipid mediated nm23-h1 plamid transfecting adnoid cystic carcinoma can gain small range positive expression, but the results give little prospect for further clinical treatment in such a manner.</p>


Subject(s)
Animals , Humans , Mice , Carcinoma, Adenoid Cystic , Lipids , Mice, Nude , NM23 Nucleoside Diphosphate Kinases , Nucleoside-Diphosphate Kinase , Plasmids , Transfection
17.
West China Journal of Stomatology ; (6): 362-365, 2004.
Article in Chinese | WPRIM | ID: wpr-330047

ABSTRACT

<p><b>OBJECTIVE</b>To look for the best carrier for cultivating oral tissue engineered mucosa.</p><p><b>METHODS</b>A series of membrane of scaffold materials of polycleclide-co-plycoclide (PLGA) were studied on their weight and biocompatibility after they had been implanted subcutaneously in rabbits for 1, 2, 3, 4 weeks respectively.</p><p><b>RESULTS</b>PLGA I , II, III degraded completely in rabbits after 2, 3, 4 weeks respectively. The other PLGA membrane degraded about 50% after 4 weeks. Histologically, the reactions of PLGA I, II, III with surrounding tissues were normal and membranes had a good biocompatibility.</p><p><b>CONCLUSION</b>The biodegrading rate of PLGA II is suitable for clinic practice. PLGA II was a promising carrier for oral tissue-engineered mucosa due to its excellent biocompatibility and biodegrading rate.</p>


Subject(s)
Animals , Female , Male , Rabbits , Absorbable Implants , Biocompatible Materials , Cells, Cultured , Lactic Acid , Metabolism , Mouth Mucosa , Cell Biology , Metabolism , Polyglycolic Acid , Metabolism , Polymers , Metabolism , Tissue Engineering
18.
West China Journal of Stomatology ; (6): 373-389, 2004.
Article in Chinese | WPRIM | ID: wpr-330044

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the variety of proliferating ability of umbilical endothelia (UE) transfected by plasmid pBABE-HYGR-hTERT.</p><p><b>METHODS</b>UE was identified from two aspects: morphology and CD34 labeling technique. The plasmid was obtained and identified by alkali splitting and gel electrophoresis. Liposomes were used to transfect UE. RT-PCR based telomeric repeat amplification protocol (TRAP) assay was used to measure the telomerase activity of endothelia.</p><p><b>RESULTS</b>UE arranged as "cobblestone" and were positive of CD34 labeling. Endothelia transfected by pBABE-HYGR-hTERT(HC) had an raised absorbance of 0.889. The shape of growth curve of HC was similar to UE. But the absorbance of MTT test and the amount of HC were prior to UE at every measuring time and the amount of HC increased four times within 8 days (P < 0.05).</p><p><b>CONCLUSION</b>The transfection of pBABE-HYGRO-hTERT had greatly improved the proliferating abilities and activated the telomerase of UE.</p>


Subject(s)
Humans , Catalytic Domain , Genetics , Cells, Cultured , Endothelium, Vascular , Cell Biology , Telomerase , Genetics , Transfection , Umbilical Veins , Cell Biology
19.
Chinese Journal of Stomatology ; (12): 277-279, 2004.
Article in Chinese | WPRIM | ID: wpr-263393

ABSTRACT

<p><b>OBJECTIVE</b>To study the growth way of parotid pleomorphic adenoma and the relative factors.</p><p><b>METHODS</b>The histological slides of 97 cases of the primary parotid pleomorphic adenoma were examined for the state of intra-capsule infiltration and extra-infiltration. The relative relationships between the infiltration state and the histological type, relative amount of various components, size and course of the tumor were analysed to investigate the growth way and relative factors.</p><p><b>RESULTS</b>1. There were more chances to develop infiltration of tumor in which the major content was epithelium. The tumor was severer with the increasing of epithelium, and decreasing of mucous content and elongation of course of the disease. 2. The limitation of the extra-envelop infiltration and budding was 0.085 - 0.210 mm, so, the boundary of partial parotidectomy should be away from the 1 cm envelop.</p><p><b>CONCLUSION</b>The growth way of parotid pleomorphic adenoma is related to the histological types and characters, relative amount of various components and the course of the tumor.</p>


Subject(s)
Adolescent , Adult , Aged , Child , Female , Humans , Male , Middle Aged , Adaptation, Physiological , Adenoma, Pleomorphic , Pathology , General Surgery , Oral Surgical Procedures , Methods , Parotid Gland , Pathology , General Surgery , Parotid Neoplasms , Pathology , General Surgery
20.
West China Journal of Stomatology ; (6): 109-111, 2004.
Article in Chinese | WPRIM | ID: wpr-319045

ABSTRACT

<p><b>OBJECTIVE</b>To study the effect of nm23-h1 transfection on proliferation characteristics of adnoid carcinoma cell lines in vitro and in vivo.</p><p><b>METHODS</b>In vitro ACC-M cell lines were incubated after putative anti-metastatic gene nm23-h1 was introduced into the cells with the help of G418 selective incubation base. The ACC-M cells were transplanted into 10 BALB/C nude mices subcutaneously and non-transfected cell lines were taken as control. Immunohisto chemistry and Ki67 antibody were employed to study the proliferation character of cell crawling pieces and paraffin-bedded slice, meanwhile, the solid tumor of both groups were prepared for flow cytometry(FCM).</p><p><b>RESULTS</b>Transfected cells grew slower than non-transfected cells and this trend became more obvious as passages passed on. In vitro the expression of Ki67 of transfected cells was little stronger than non-transfected cells, while the expression of Ki67 in solid slices was almost negative in both groups. Transfected cells presented slower growth than non-transfected cells in the early stage (2 weeks) and 2 weeks later there was no obvious difference in size(P > 0.05). FCM value accorded well with the result.</p><p><b>CONCLUSION</b>Introduction of nm23-h1 into the ACC-M cell lines may have transient inhibitory effects on its proliferation.</p>


Subject(s)
Animals , Female , Mice , Antibodies , Carcinoma, Adenoid Cystic , Genetics , Pathology , Cell Division , Cell Line, Tumor , Genetic Therapy , Ki-67 Antigen , Allergy and Immunology , Mice, Inbred BALB C , Mice, Nude , Mouth Neoplasms , Genetics , Pathology , NM23 Nucleoside Diphosphate Kinases , Neoplasm Transplantation , Nucleoside-Diphosphate Kinase , Proteins , Genetics , Transfection
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