1.Epithelial-stromal tumor of seminal vesicle: report of a case.
Ai-hua HUANG ; Ya-bo GAO ; Mei JIN
Chinese Journal of Pathology 2010;39(1):55-56
Diagnosis, Differential
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Genital Neoplasms, Male
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metabolism
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pathology
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surgery
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Humans
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Male
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Middle Aged
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Neoplasms, Glandular and Epithelial
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metabolism
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pathology
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surgery
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Neprilysin
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metabolism
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Receptors, Estrogen
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metabolism
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Receptors, Progesterone
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metabolism
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Seminal Vesicles
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Stromal Cells
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pathology
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Vimentin
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metabolism
2.Comparative proteomics study of different processing technology for pilose antler using iTRAQ technology coupled with 2D LC-MS.
Meng-ya JIN ; Ling DONG ; Yuan-ming LUO ; Li YU ; Mei MO ; Cheng-bo HOU ; Zhi-yuan LI
Acta Pharmaceutica Sinica 2015;50(12):1637-1644
This study was designed to use iTRAQ technology coupled with 2D LC-MS/MS to study the comparative proteomics of different processing technology for pilose antler. 1015 proteins were identified with 2D LC combined with MOLDI TOF/TOF mass spectrometry. Comparative analysis with Protein Pilot (Version 4.5) revealed that 87 proteins were changed (P ≤ 0.05, the ratio of > 1.50 or < 0.60 as the threshold selection of difference proteins), of which 24 were up regulated and 33 were down regulated in the traditional frying process (TFP) compared with the fresh pilose antler (P ≤ 0.05). 7 significant different proteins (P ≤ 0.001), most of these significantly changed proteins were found to be involved in calcium ion binding and ATP binding associated with human healthy. Freeze drying with protective agent (FDP) (Trehalose) can improve the content of significantly different proteins (P ≤ 0.001) including Collagen alpha-1 (XII) chain (COL12A1) and Collagen alpha-1 (II) chain (COL2A1). The significant function involves in platelets activating, maintenance of spermatogonium, and disorder expression in tumor cells. The functional annotation by Hierarchical clustering and GO (gene ontology) showed that the main molecule functions of the proteins significantly changed in these processes were involved in binding (52.7%), catalytic (25.3%), structural molecule and transporter (6.6%).
Animals
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Antlers
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chemistry
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Chromatography, Liquid
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Collagen
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chemistry
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Down-Regulation
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Freeze Drying
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Gene Expression Regulation
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Proteomics
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Tandem Mass Spectrometry
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Technology, Pharmaceutical
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methods
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Up-Regulation
3.Correlation analysis between plasma D-dimer levels and orthopedic trauma severity.
Li-Dan ZHANG ; Hong-Bo LIU ; Yu-Neng LI ; Hai-Mei MA ; Ya-Bo LIU ; Man-Yi WANG
Chinese Medical Journal 2012;125(17):3133-3136
BACKGROUNDThe correlation between the plasma D-dimer level and deep vein thrombosis has not been conclusive in various studies. The aim of this research was to study the relationship between plasma D-dimer levels and the severity of orthopedic trauma by retrospective examination of orthopedic trauma cases.
METHODSClinically acute trauma and non-acute trauma patients were selected and their plasma D-dimer levels were measured. Plasma D-dimer levels in patients of these two groups were compared. The relationship between the plasma D-dimer level and the severity of the trauma was also studied.
RESULTSThere were 548 cases in the acute trauma group and 501 cases in the non-acute trauma group. The levels of plasma D-dimer were significantly higher in the acute trauma group than in the non-acute trauma group (P < 0.01). In the acute trauma group, the correlation between the D-dimer level and the number of fractures was a positive linear correlation (r = 0.9532).
CONCLUSIONSElevated plasma D-dimer is common in trauma patients. The D-dimer level and the number of fractures in the trauma patients are closely correlated. D-dimer is not only an indicator for the diagnosis of deep vein thrombosis and pulmonary embolus, but also an indicator of the severity of trauma in acute trauma patients.
Acute Disease ; Adult ; Female ; Fibrin Fibrinogen Degradation Products ; analysis ; Humans ; Male ; Middle Aged ; Pulmonary Embolism ; blood ; Retrospective Studies ; Severity of Illness Index ; Venous Thrombosis ; blood ; Wounds and Injuries ; blood
4.Cloning, purification, and antigenic characterization of three recombinant fragments derived from SARS-CoV S1 domain.
Ya-bo MEI ; Zhi-yong LIAO ; Ya-di WANG ; Li-ya ZHANG ; Hua XU ; Kwok-yung YUEN ; Xiao-yan CHE
Chinese Journal of Experimental and Clinical Virology 2005;19(3):275-278
OBJECTIVEThe present study aimed to clone and express three fragments of genomic RNA derived from SARS associated coronavirus (SARS-CoV) S1 domain and to study its immunogenicity.
METHODSThe S1 domain gene was amplified by PCR with specific primers and was inserted into the prokaryotic expression vector pQE-30. Three fragments (40-751, 746-1344 and 746-2001 bp) derived from S1 domain produced after the recombinant plasmid (pQE-30/S1) was digested by restriction endonucleases. The three fragments were cloned into pQE-30 and expressed in M15 strains of Escherichia coli. The expression products, designated S1a, S1b and S1c respectively, were purified by Ni affinity chromatography. The immunogenicity was analyzed by Western Blot and ELISA using serologically confirmed sera from SARS patients and the sera from healthy donors was used as control at the same assay.
RESULTSThree recombinant plasmids (pQE-30/S1a, pQE-30/S1b, pQE-30/S1c) were constructed.Fusion proteins with relative molecular mass of 26,700, 22,500 and 46,000 dalton were successfully expressed with amounts of 35%, 35% and 30% of total cell protein and purified by Ni affinity chromatography, respectively. Western Blot and ELISA analysis showed that the S1c protein could be specifically recognized by the sera from SARS patients.
CONCLUSIONThe recombinant S1c protein was a good immunogen and has the potential to be used as a vaccine against SARS-CoV infection.
Antibodies, Viral ; blood ; Antigens, Surface ; genetics ; immunology ; metabolism ; Blotting, Western ; Electrophoresis, Polyacrylamide Gel ; Enzyme-Linked Immunosorbent Assay ; Humans ; Immunoglobulin G ; blood ; Immunoglobulin M ; blood ; Plasmids ; genetics ; Polymerase Chain Reaction ; Recombinant Proteins ; immunology ; isolation & purification ; metabolism ; SARS Virus ; genetics ; immunology ; metabolism ; Severe Acute Respiratory Syndrome ; blood ; virology ; Viral Envelope Proteins ; genetics ; immunology ; metabolism
5.Study of serological biochemistry index of chronic periodontitis.
Xue ZHAO ; Ya-ping PAN ; Dong-mei ZHANG ; Jing-bo LIU
West China Journal of Stomatology 2010;28(6):584-598
OBJECTIVETo investigate the effect of serum biochemistry on the development of periodontitis.
METHODS225 participants without any system disease were involved in the study. Case group consist of 145 chronic peri-odontitis and was divided into gentle group (clinical attachment loss < 3 mm), moderate and severe group(clinical attachment loss > or = 3 mm). Control group consist of 80 periodontal healthy persons. Peripheral blood sample was obtained from each subject by venipuncture. Serum chemistry variables including glucose, lipid and calcium were analyzed. SPSS 12.0 software package was adopted to analyze the investigation results.
RESULTSThere's no statistically significant difference of serum, lipid and calcium between case group and control group (P > 0.05). But case group had a higher percentage of people with abnormal glucose, lipid and calcium than control group (P < 0.05). Moderate and severe group had a significantly higher serum glucose, triglyceride and lipoproteins-cholesterol than gentle group (P < 0.05).
CONCLUSIONAbnormal level of serum glucose, lipid and calcium may increase the affectability of host to periodontitis and promote the inflammation in paradentium.
Cholesterol ; Chronic Periodontitis ; Female ; Humans ; Lipids ; Lipoproteins ; Periodontitis ; Triglycerides
6.Analysis of the differences in the expression of HSP27 and c-kit between benign prostatic hyperplasia and prostatic cancer tissues.
Bo ZHEN ; Ya SHEN ; Yue-Mei ZHANG ; Chang-Hong ZHU ; Zi-Long LIU
National Journal of Andrology 2006;12(5):416-420
OBJECTIVETo examine the differences in the expression of HSP27 and c-kit between benign prostatic hyperplasia (BPH) and prostatic cancer (PCa) tissues and to analyse the relationship between their expression and BPH and PCa, especially the relationship with the occurrence, development, prognosis and treatment of PCa.
METHODSAn immunohistochemical staining (SP method) for HSP27 and c-kit was undertaken on 40 BPH and 40 PCa tissues samples.
RESULTSConsistent patterns of cytoplasmic staining for HSP27 were seen in all sections of tissue from BPH. The glandular epithelium stained very strongly positively and the stroma stained positively. The staining for HSP27 in PCa tissues was located in the cytoplasm of glandular epithelia, but the expression of HSP27 in PCa was higher than BPH (P < 0.05). The staining for c-kit in BPH tissues was located in the cytoplasm of smooth muscle cells, and in PCa tissues was located in epithelial cells. The expression of c-kit in PCa tissues was lower than BPH (P < 0.05). The expression level of both HSP27 and c-kit were decreased with the development of grade of PCa (P < 0.05); HSP27 was increased with the development of clinical stage of PCa (P < 0.05 ); c-kit was decreased with the development of clinical stage of PCa (P < 0.05).
CONCLUSIONThe expression level of HSP27 and c-kit was highly correlated with the process of the development from BPH to PCa, and also correlated with tumor grades and stages. The expression of HSP27 and c-kit may be used as an important pathological index and may be helpful for the treatment of PCa.
Aged ; Aged, 80 and over ; HSP27 Heat-Shock Proteins ; Heat-Shock Proteins ; biosynthesis ; Humans ; Immunohistochemistry ; Male ; Middle Aged ; Neoplasm Proteins ; biosynthesis ; Prostatic Hyperplasia ; metabolism ; pathology ; Prostatic Neoplasms ; metabolism ; pathology ; Proto-Oncogene Proteins c-kit ; biosynthesis
7.A case report of propionic academia.
Ya-Bo MEI ; Hai-Hong LIU ; Chun-Zhi WANG ; Xi-Yu HE ; Zhi-Chun FENG
Chinese Journal of Contemporary Pediatrics 2010;12(10):838-839
Female
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Humans
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Infant
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Propionic Acidemia
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diagnosis
8.Health condition of workers exposed to silica dust in 6 quartz processing industry enterprises in Lianyungang city.
Ya-ping HUO ; Ri-hui ZHOU ; Bo SUN ; Bao-li ZHU ; Ru-yan YNAG ; Fang-wen GONG ; Li-zhuang XIE ; Bang-mei DING
Chinese Journal of Industrial Hygiene and Occupational Diseases 2013;31(11):849-850
Adolescent
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Adult
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Dust
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analysis
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Female
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Health Status
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Humans
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Industry
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Male
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Middle Aged
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Occupational Exposure
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analysis
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Quartz
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Young Adult
9.Genotype and sequence analysis on G2 segments of hantavirus from HFRS patients in Hebei Province.
Qi LI ; Ya-mei WEI ; Zhan-ying HAN ; Yan-bo ZHANG ; Shun-xiang QI ; Yong-gang XU
Chinese Journal of Experimental and Clinical Virology 2008;22(1):15-17
OBJECTIVETo know the genotype and subtype of hantavirus (HV) which infected persons in Hebei province.
METHODSAccording to G2 coding region of 76-118 and R22 strains, specific type primers were designed to detect and identity the types of HV in HFRS patients' sera with RT-nested PCR. Nucleotides were assayed from partial products after purification and reclaim. Then, gene analysis was done with DNAStar package.
RESULTS17 out of 69 positive serum specimens were successfully detected by RT-PCR and the detection rate was 24.64%, among which,
CONCLUSIONSEO was the major type of HV from HFRS patients in Hebei province, S3 was the major subtype and S1 was also existed. In a certain area, the HV which belonged to the same type was correspondingly conservative, and had the characteristic of regional stability.
China ; Genotype ; Hantavirus ; classification ; genetics ; Hemorrhagic Fever with Renal Syndrome ; diagnosis ; prevention & control ; therapy ; virology ; Humans ; Phylogeny ; Reverse Transcriptase Polymerase Chain Reaction ; Sequence Analysis, DNA ; Viral Envelope Proteins ; genetics
10.Morphological study and Ca/P ratio analysis of Er, Cr:YSGG laser irradiation on periodontal diseased root surfaces.
Shu-ping SUN ; Ya-ping PAN ; Dong-mei ZHANG ; Bo ZOU
West China Journal of Stomatology 2006;24(5):444-446
OBJECTIVETo observe the morphological transformation and Ca/P changes of the periodontally disease root surfaces irradiated by Er, Gr:YSGG Laser.
METHODS18 periodontally diseased teeth and 6 wisdom teeth were collected in vitro. After 18 periodontally diseased teeth were planed, 12 teeth were randomly selected as the laser treatment group, the others as the acid treatment group. The 6 wisdom teeth were selected as the healthy control. Then the evaluation for root surfaces morphological transformation was conducted by SEM. An energy spectrum analyzer was used to analyze the Ca/P ratio of root surfaces.
RESULTSThe root surfaces were clean and even in the laser treatment group. Smear layer could also be effectively eliminated in the laser treatment group and the acid treatment group, but the SEM results were different. Atom content analysis showed that the Ca/P ratio of the laser treatment group and the acid treatment group had no distinct difference.
CONCLUSIONIt is effective to remove smear layers and infected cementum of surface layers with Er, Cr:YSGG irradiating on the planed periodontal root surfaces.
Cell Adhesion ; Dental Cementum ; Humans ; Lasers, Solid-State ; Microscopy, Electron, Scanning ; Periodontal Diseases ; Root Planing ; Smear Layer ; Tooth Root