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1.
Chinese Journal of Gastrointestinal Surgery ; (12): 1077-1080, 2016.
Article in Chinese | WPRIM | ID: wpr-323531

ABSTRACT

The death of patients with gastric cancer is mainly due to its recurrence and metastasis, and circulating tumor cell (CTC) is the necessary condition of metastasis. As liquid biopsy, CTC detection has its certain clinical significance. The detection is required after enrichment because circulating tumor cells are rare. Many enrichment methods have been developed: methods based on physical characteristics of TCT, like density, size and dielectric properties and so on; immunogenicity, like Cell Search System; and microfluidic chip technology. The immunofluorescence is commonly used to identify CTC in gastric cancer and the isolated CTC can also be used for the following analysis on the level of nucleic acid, protein and gene regulation. Detection of CTC in gastric cancer is helpful to judge the prognosis, assess staging, monitor the curative effect and guide the development of drug. There are many challenges for clinical transformation of CTC: the lower enrichment efficiency, the less specific surface markers, the uncertain diagnostic efficiency and so on, but it also has the good research prospect because it is non-invasive, repeatable and can real-time monitor the condition and guide the clinical treatment compared with pathological biopsy. In this paper, the detection and identification methods, and clinical value of CTC in gastric cancer patients are reviewed.


Subject(s)
Humans , Biomarkers, Tumor , Biopsy , Cell Separation , Methods , Cytodiagnosis , Methods , Flow Cytometry , Methods , Fluorescent Antibody Technique , Methods , Microchip Analytical Procedures , Methods , Neoplasm Recurrence, Local , Neoplasm Staging , Methods , Neoplastic Cells, Circulating , Metabolism , Pathology , Prognosis , Secondary Prevention , Stomach Neoplasms , Blood , Diagnosis , Genetics , Therapeutics , Treatment Outcome
2.
Chinese Journal of Medical Instrumentation ; (6): 355-357, 2013.
Article in Chinese | WPRIM | ID: wpr-264190

ABSTRACT

Biochip analytical technology shows high throughput property for multi-samples measurement, so can reduce the required amount of samples and time used for determination. The technology quickly developed in recent years and has been applied in medical diagnosis and other analytical areas including gene chip, protein chip, lab-on-a-chip, tissue microarray, cell microarray, carbohydrate microarray and so on. This paper overviewed the current development of biochip technology, and explored the perspective of its application.


Subject(s)
Diagnostic Techniques and Procedures , Microchip Analytical Procedures , Methods
3.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 920-923, 2013.
Article in Chinese | WPRIM | ID: wpr-359315

ABSTRACT

<p><b>OBJECTIVE</b>To study the expression changes of tumor necrosis factor-alpha (TNF-(alpha), interleukin-6 (IL-6), C-reactive protein (CRP), monocyte chemotactic protein 1 (MCP-1), and their correlation with obesity in 20 -50 years old population of phlegm-damp constitution (PDC) and of normal constitution (NC) using Luminex technique.</p><p><b>METHODS</b>Totally 101 population were recruited from Health Examination Center of Puren Hospital from April to December 2011. Based on body mass index (BMI), the subjects were assigned to four groups, i.e., the obesity of PDC group (Group OBT, BMI > or = 24 kg/m2, 30 cases), the non-obesity of PDC group (Group NOBT, BMI < 24 kg/m2, 25 cases), the obesity of non-PDC group (Group OBNT, BMI > or = 24 kg/m2, 28 cases), the NC group (Group P, BMI < 24 kg/m2, 18 cases). The BMI and body fat percent (FAT%) were compared among the 4 groups. Serum levels of TNF-alpha, IL-6, CRP, and MCP-1 were measured with Luminex technique.</p><p><b>RESULTS</b>BMI was significantly higher in Group OBT and Group OBNT than in Group NOBT and Group P (all P < 0.05). The FAT% was significantly higher in Group OBT and Group OBNT than in Group P (P < 0.01). The serum TNF-alpha level in Group OBT was higher than in Group P (P < 0.01). The serum CRP and MCP-1 levels were significantly higher in Group OBT, NOBT, and OBNT than in Group P (P < 0.05, P < 0.01). The score for PDC was positively correlated with TNF-alpha, IL-6, and MCP-1 levels (P < 0.05).</p><p><b>CONCLUSIONS</b>Abnormal higher levels of inflammatory factors exist in 20 -50 years old population of PDC. Chronic inflammation exists in population of PDC and obesity people.</p>


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Young Adult , Body Mass Index , C-Reactive Protein , Metabolism , Case-Control Studies , Chemokine CCL2 , Blood , Inflammation , Interleukin-6 , Blood , Medicine, Chinese Traditional , Microchip Analytical Procedures , Obesity , Blood , Diagnosis , Tumor Necrosis Factor-alpha , Blood
4.
Journal of Zhejiang University. Medical sciences ; (6): 75-80, 2012.
Article in Chinese | WPRIM | ID: wpr-247180

ABSTRACT

<p><b>OBJECTIVE</b>To screen differentially expressed microRNAs in bone marrow-derived mesenchymal stem cells (BMMSCs) during osteoporosis and their function in stem cell differentiation.</p><p><b>METHODS</b>The osteoporosis model was induced by ovariectomy in mice.The differentially expressed microRNAs in BMMSCs during osteoporosis were screened with microRNA microarray chip and their expressions during osteogenesis and adipogenesis were detected by RT-PCR.</p><p><b>RESULTS</b>Ten differentially expressed microRNAs were detected in BMMSC during osteoporosis. The expression of 5 specific microRNAs altered significantly during osteogenic differentiation and 3 microRNAs altered during adipogenic differentiation.</p><p><b>CONCLUSION</b>A serials of differentially expressed microRNAs may be involved in functional defects of BMMSC during osteoporosis.</p>


Subject(s)
Animals , Female , Mice , Bone Marrow Cells , Cell Biology , Metabolism , Cell Differentiation , Disease Models, Animal , Gene Expression Profiling , Mesenchymal Stem Cells , Cell Biology , Metabolism , Mice, Inbred C57BL , MicroRNAs , Metabolism , Microchip Analytical Procedures , Osteoporosis , Metabolism
5.
Chinese Journal of Hepatology ; (12): 785-788, 2012.
Article in Chinese | WPRIM | ID: wpr-296814

ABSTRACT

<p><b>OBJECTIVE</b>To develop an early and accurate detection method for hepatocellular carcinoma (HCC) based on detection of tumor-associated serum markers using a multiplex quantitative antibody array.</p><p><b>METHODS</b>The double-antibody sandwich principle was used to establish an antibody array composed of eight cancer-related serum markers, including alpha-fetoprotein (AFP), hepatocyte growth factor (HGF), insulin-like growth factor (IGF), interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10 (IL-10), transforming growth factor-beta 1 (TGF-b1), and vascular endothelial growth factor (VEGF). Serum samples from 160 cases of clinically diagnosed HCC and from 58 cases of liver cirrhosis (LC; controls) were obtained to test the array. Sixty percent of the samples were randomly selected for use as the training set (HCC, n = 96; LC, n = 36), and the remaining 40% was used as the test set (HCC, n = 64; LC, n = 22). The SPSS statistical software was used to perform logistic regression analysis and to create a diagnostic model.</p><p><b>RESULTS</b>When used with the training set, the model had sensitivity of 93.3%, specificity of 83.3%, and accuracy of 90.9%. When used with the test set, the model had sensitivity of 89.0%, specificity of 77.3%, and accuracy of 86.0%. The traditional serum AFP value (cut-off value of 20 ng/mL) showed 70.0% diagnostic sensitivity, 59.0% specificity, and 64.0% accuracy.</p><p><b>CONCLUSION</b>The newly developed multiplex quantitative antibody detection system has high sensitivity and specificity. The diagnostic model with AFP and seven other cancer-related factors was superior to the traditional AFP only approach for early diagnosis of liver cancer, indicating its potential clinical value.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult , Biomarkers, Tumor , Blood , Carcinoma, Hepatocellular , Diagnosis , Early Diagnosis , Liver Neoplasms , Diagnosis , Microchip Analytical Procedures , Sensitivity and Specificity , alpha-Fetoproteins , Allergy and Immunology
6.
Journal of Experimental Hematology ; (6): 1602-1604, 2009.
Article in Chinese | WPRIM | ID: wpr-328591

ABSTRACT

MicroRNAs (miRNAs) are small noncoding RNA molecules that negatively regulate gene expression via degradation or translational repression of their targeted mRNAs. MiRNAs are involved in critical biologic processes, including development, cell differentiation, proliferation and the pathogenesis of disease. This review focuses on recent researches on the detection techniques of miRNA including micorarray technique, Northern blot, real-time quantitative PCR, detection technique of miRNA function and so on.


Subject(s)
Blotting, Northern , MicroRNAs , Genetics , Microchip Analytical Procedures , Oligonucleotide Array Sequence Analysis , Polymerase Chain Reaction
7.
Chinese Journal of Medical Instrumentation ; (6): 434-437, 2008.
Article in Chinese | WPRIM | ID: wpr-309557

ABSTRACT

An automatic inspection system for biochip's print quality is presented in this paper. It consists of an automatic mechanical control, a CCD sensor for getting the image of PET boart, and the special computer software for image processing and recognition. Experimental results indicate that this system is capable of providing a precise and effective realtime inspection for biochips' print quality.


Subject(s)
Biosensing Techniques , Methods , Equipment Design , Image Processing, Computer-Assisted , Methods , Microchip Analytical Procedures , Methods , Pattern Recognition, Automated , Methods , Quality Control , Software
8.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery ; (24): 1081-1084, 2007.
Article in Chinese | WPRIM | ID: wpr-747582

ABSTRACT

OBJECTIVE@#To evaluate the expression of PTEN in squamous cell carcinoma of larynx and its relationship with factors like pathologic fractionation, clinical TNM stage, and prognosis by the tissue chip technology.@*METHOD@#We studied the expression of PTEN gene and its mRNA on a series of 146 cases of primary laryngeal carcinoma patients, 40 cases of precancerous lesion and 26 cases of vocal fold polyp by tissue chip by, immunohistochemistry and in situ hybridization method. The observed data observed and some relevant clinical dada were statistically analyzed.@*RESULT@#The expression of PTEN in vocal fold polyp was negative, and its positive expression in precancerous lesion and laryngeal carcinoma were 40% and 43.15% respectively by immunohistochemistry, and were 72.50 and 59.59% respectively in situ hybridization. The difference between the expression of PTEN in laryngeal carcinoma and its pathological fraction and prognosis was statistically significant, but was not significant between that and location, clinical stage and LN metastasis. The mRNA expression of PTEN was higher than that of the protein expression in precancerous lesion and cancer tissue.@*CONCLUSION@#The tissue microarray technique required shorter time and less expense, and showed higher consistency in our essays. And the present study suggests PTEN was a prognosis factor of the Laryngeal carcinoma.


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Carcinoma, Squamous Cell , Metabolism , Pathology , Laryngeal Neoplasms , Metabolism , Pathology , Larynx , Metabolism , Pathology , Microchip Analytical Procedures , Neoplasm Staging , PTEN Phosphohydrolase , Metabolism
9.
National Journal of Andrology ; (12): 629-632, 2006.
Article in Chinese | WPRIM | ID: wpr-343556

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the expression of gene BRG1 in prostatic intraepithelial neoplasia and adenocarcinoma, and the relationship between gene BRG1 expression and the clinicopathological features of prostate carcinoma.</p><p><b>METHODS</b>Gene BRG1 expression was evaluated in 37 cases of human prostate carcinoma, 13 human prostatic intraepithelial neoplasia (PIN) and 14 human benign prostatic hyperplasia (BPH) by using immunohistochemistry (EnVision method) and tissue microarray.</p><p><b>RESULTS</b>The positive rates of BRG1 protein were 81.08% (30/37), 38.46% (5/13) and 14.28% (2/14) in prostate carcinoma, PIN and BPH, respectively, significantly higher in the first group than in the latter two (P < 0.05). There was no statistically significant difference in BRG1 gene expression either between PIN and BPH (P > 0.05) or between the groups of the moderate differentiation (the Gleason histologic grading: 5-7) and the lower one (the Gleason histologic grading: 8-10) (P > 0.05).</p><p><b>CONCLUSION</b>BRG1 may play an important role in the development of prostate carcinoma. Tissue microarray technology, with the advantages of high throughput, conciseness, rapidity, high efficiency, low cost, and nice reproducibility, has significant practical value and broad application prospects in pathology.</p>


Subject(s)
Aged , Aged, 80 and over , Humans , Male , Middle Aged , DNA Helicases , Immunohistochemistry , Microchip Analytical Procedures , Nuclear Proteins , Prostatic Neoplasms , Metabolism , Pathology , Reproducibility of Results , Transcription Factors
10.
Journal of Biomedical Engineering ; (6): 216-219, 2006.
Article in Chinese | WPRIM | ID: wpr-309850

ABSTRACT

This paper introduces the new research achievement and progress of electro-physiology in olfaction and gustation. Classical implements such as patch-clamp or glass pipette are not appropriate in the dynamic detection of cellular signal transportation. In view of this, we have analyzed the feasibilities and challenges of olfactory or gustatory cell-based biosensors such as field effect transistor (FET) and light addressable potentiometric sensor (LAPS). Finally we present the research work carried our in out lab and a future prospective on the development in this field.


Subject(s)
Humans , Biosensing Techniques , Methods , Electrophysiology , Methods , Microchip Analytical Procedures , Methods , Smell , Physiology , Taste , Physiology
11.
Journal of Biomedical Engineering ; (6): 160-162, 2005.
Article in Chinese | WPRIM | ID: wpr-327110

ABSTRACT

This paper deals with the manufacturing state of the art of biochip, and introduces a new method--laser microtechnology, including its developing procedure, characteristics and function in biochip production.


Subject(s)
Biosensing Techniques , Methods , Computer-Aided Design , Equipment Design , Lab-On-A-Chip Devices , Lasers , Microchip Analytical Procedures , Methods , Micromanipulation
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