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1.
Chinese Journal of Preventive Medicine ; (12): 95-98, 2022.
Article in Chinese | WPRIM | ID: wpr-935255

ABSTRACT

Exploring a new teaching mode of CHB laboratory diagnostics to improve the teaching quality through establishment a teaching model covered the whole process of CHB disease diagnosis and differential diagnosis, treatment, drug selection, the toxicity and side effects prediction, effect monitoring, and prognosis evaluation. According to the CHB clinical diagnosis and treatment guidelines, formulated the laboratory examination and detection strategies related to different stages of CHB, and established CHB clinical laboratory diagnostic pathway. Compared the classroom teaching effect by the questionnaire between the 2016 and 2017 eight-year undergraduates from the First Clinical College of Wuhan University. In this study,the CHB clinical laboratory diagnostic pathway was established and approved by clinicians, which covered the whole process of CHB disease diagnosis and differential diagnosis, treatment, drug selection, the toxicity and side effects prediction, effect monitoring, and prognosis evaluation. The teaching quality evaluation indicators and the scores on the class test had been greatly improved with the clinical diagnostic pathway teaching mode in the classroom teaching of 2017 clinical medicine undergraduates compared with the traditional teaching mode in the 2016 clinical medicine undergraduates. In summary, the medical students not only could realize the organic integration of laboratory diagnostics and clinical medicine, but also improves overall understanding of various laboratory tests in CHB diagnosis and treatment from the teaching model of laboratory diagnostics based on the CHB clinical laboratory diagnostic pathway,and the quality of teaching for CHB has been significantly improved.


Subject(s)
Humans , Clinical Laboratory Techniques , Hepatitis B, Chronic , Laboratories , Laboratories, Clinical , Records
2.
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 758-766, 2016.
Article in English | WPRIM | ID: wpr-238440

ABSTRACT

PKHD1 gene mutations are found responsible for autosomal recessive polycystic kidney disease (ARPKD). However, it is inconvenient to detect the mutations by common polymerase chain reaction (PCR) because the open reading frame of PKHD1 is very long. Recently, long-range (LR) PCR is demonstrated to be a more sensitive mutation screening method for PKHD1 by directly sequencing. In this study, the entire PKHD1 coding region was amplified by 29 reactions to avoid the specific PCR amplification of individual exons, which generated the size of 1 to 7 kb products by LR PCR. This method was compared to the screening method with standard direct sequencing of each individual exon of the gene by a reference laboratory in 15 patients with ARPKD. The results showed that a total of 37 genetic changes were detected with LR PCR sequencing, which included 33 variations identified by the reference laboratory with standard direct sequencing. LR PCR sequencing had 100% sensitivity, 96% specificity, and 97.0% accuracy, which were higher than those with standard direct sequencing method. In conclusion, LR PCR sequencing is a reliable method with high sensitivity, specificity and accuracy for detecting genetic variations. It also has more intronic coverage and lower cost, and is an applicable clinical method for complex genetic analyses.


Subject(s)
Humans , DNA Mutational Analysis , Exons , Genetics , Genetic Testing , Genotype , Introns , Genetics , Mutation , Polycystic Kidney, Autosomal Recessive , Diagnosis , Genetics , Polymerase Chain Reaction , Receptors, Cell Surface , Genetics , Sequence Analysis, DNA
3.
Yonsei Medical Journal ; : 428-434, 2014.
Article in English | WPRIM | ID: wpr-19544

ABSTRACT

PURPOSE: To analyze the correlation of polymorphisms of toll-like receptor 7 (TLR7) (rs179009) and toll-like receptor 9 (TLR9) (rs187084) in hepatitis C virus (HCV) infections in the Han population. MATERIALS AND METHODS: The genotypes of TLR7IVS2-151 in HCV infection were detected by Sanger sequencing using polymerase chain reaction-restriction fragment length polymorphism to determine the TLR9 T-1486C single nucleotide polymorphisms (SNP) for all enrolled patients. RESULTS: We found no significant difference between males with spontaneous clearance of HCV versus those chronically infected [chi2=2.71, p=0.10, odd ratios (OR)=0.58, 95% confidence interval (CI) 0.31-1.11]. However, significant differences were found for the distribution of TLR7 (rs179009) in females (chi2=9.46, p=0.01). In females, a significant difference was also found between chronic hepatitis C and those with spontaneous clearance of HCV in terms of TLR7 IVS2-151G/A allele frequencies (chi2=9.50, p=0.00, OR=0.46, 95% CI 0.28-0.75). In HCV-infected patients, no significant association was found between the frequency of TLR9 genotypes and alleles. CONCLUSION: The site of TLR7 IVS2-151 (rs179009) G/A may be a factor for susceptibility of chronic HCV in the female Han population. TLR9T-1486C (rs18084) SNP may not play a major role in HCV infection. However, individual risk profiles for HCV infection did vary by sex and this relationship should be further investigated.


Subject(s)
Female , Humans , Male , Alleles , China , Confidence Intervals , Gene Frequency , Genotype , Hepacivirus , Hepatitis C , Hepatitis C, Chronic , Hepatitis , Methods , Polymorphism, Single Nucleotide , Toll-Like Receptor 7 , Toll-Like Receptor 9 , Toll-Like Receptors
4.
Chinese Journal of Cancer ; (12): 842-852, 2011.
Article in English | WPRIM | ID: wpr-294451

ABSTRACT

Our previous study revealed that spaceflight induced biological changes in human cervical carcinoma Caski cells. Here, we report that 48A9 cells, which were subcloned from Caski cells, experienced significant growth suppression and exhibited low tumorigenic ability after spaceflight. To further understand the potential mechanism at the transcriptional level, we compared gene expression between 48A9 cells and ground control Caski cells with suppression subtractive hybridization (SSH) and reverse Northern blotting methods, and analyzed the relative gene network and molecular functions with the Ingenuity Pathways Analysis (IPA) program. We found 5 genes, SUB1, SGEF, MALAT-1, MYL6, and MT-CO2, to be up-regulated and identified 3 new cDNAs, termed B4, B5, and C4, in 48A9 cells. In addition, we also identified the two most significant gene networks to indicate the function of these genes using the IPA program. To our knowledge, our results show for the first time that spaceflight can reduce the growth of tumor cells, and we also provide a new model for oncogenesis study.


Subject(s)
Female , Humans , Blotting, Northern , Methods , Cell Line, Tumor , Cell Proliferation , Gene Expression Profiling , Gene Expression Regulation, Neoplastic , Gene Library , Gene Regulatory Networks , Nucleic Acid Hybridization , Methods , Space Flight , Up-Regulation , Uterine Cervical Neoplasms , Genetics , Pathology
5.
Journal of Central South University(Medical Sciences) ; (12): 233-237, 2008.
Article in Chinese | WPRIM | ID: wpr-814090

ABSTRACT

OBJECTIVE@#To investigate whether there are autoantibodies to nasopharyngeal carcinoma (NPC) in the sera of patients and to find new NPC biomarkers.@*METHODS@#Cell plate of Epstein Barr virus negative NPC cell line CNE1 was prepared, and difference between 32 NPC patient sera and 54 normal sera was analyzed by ELISA. We extracted the total protein of CNE1, and analyzed whether there were specific proteins to react with NPC sera by Western blot.@*RESULTS@#The average absorbance values of serum antibody in NPC patients (0.904+/-0.032) were significantly higher than those of normal serum antibody absorbance values (0.736+/-0.028) (P< 0.01). The analysis with Western blot showed there were positive bands,and some of these were unanimous bands, but the intensity increased, and some of these were new bands compared with the normal sera. These positive bands may be NPC tumor-associated antigens or NPC tumor-specific antigens.@*CONCLUSION@#Autoantibodies that react with NPC exist in the sera of NPC patients, but they do not react with Epstein-Barr virus. It provides the basis to seek the tumor biomarkers in NPC sera.


Subject(s)
Humans , Antigens, Neoplasm , Allergy and Immunology , Autoantibodies , Blood , Biomarkers, Tumor , Blood , Nasopharyngeal Neoplasms , Diagnosis , Allergy and Immunology
6.
Chinese Journal of Stomatology ; (12): 353-354, 2007.
Article in Chinese | WPRIM | ID: wpr-333322

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the periodontal conditions after the wedge-shaped defect was restored by gingival retraction technique.</p><p><b>METHODS</b>A total of 138 mandibular premolars with wedge-shaped defect were selected and divided into A, B groups. Group A was restored with Dyract after using retraction cord. Group B was directly restored with Dyract. Clinical parameters including plaque index (PLI), gingival index (GI), sulcus bleeding index (SBI), probing depth (PD), volumes of gingival crevicular fluid (GCF) and levels of aspartate aminotransferases (AST) of gingival crevicular fluid were measured at baseline, 1 week, 1 month, 3 months and 6 months after operation.</p><p><b>RESULTS</b>There was no difference in PLI, GI, SBI, PD between group A and B during 6 months after operation, while the difference of GCF and AST was significant between group A and B at 3 months and 6 months after operation (P < 0.05, P < 0.01).</p><p><b>CONCLUSIONS</b>Gingival retraction technique applied in wedge-shaped defect restoration can reduce the damage to the periodontal tissue.</p>


Subject(s)
Adolescent , Adult , Female , Humans , Male , Young Adult , Aspartate Aminotransferases , Dental Plaque Index , Dental Restoration, Permanent , Methods , Gingival Crevicular Fluid , Periodontal Index
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