2.Research Progress of circRNA and Its Significance in Forensic Science.
Ya-qi ZHANG ; Cheng-chen SHAO ; Cheng-tao LI ; Zi-qin ZHAO ; Jian-hui XIE
Journal of Forensic Medicine 2016;32(2):131-133
RNA has received more attention in the field of forensic medicine and the development of the new biological markers based on RNA shows great significance in the analysis of complex cases. circular RNA (circRNA) is a kind of non-coding RNA which is widely reported recently. Although the regulatory mechanisms of generation and expression are not fully clear, the existing research indicates that circRNA has important biological functions. CircRNA has a cell-type-specific expression with great stability and a high expression level, which makes it meaningful in forensic applications potentially. In this paper, the research progress, the generation and regulation of circRNA as well as its biological characteristics and functions are summarized, which will provide references for related studies and forensic applications.
Forensic Sciences
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Humans
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RNA
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RNA, Circular
3.Comparative study between MRI and echocardiography in noncompaction of ventricular myocardium
Zi-Yan SUN ; Li-Ming XIA ; Cheng-Yuan WANG ; Jing-Jing YAO ; Wei-Hui SHENTU ;
Chinese Journal of Radiology 2001;0(08):-
Objective To investigate the MRI and echocardiography manifestations of noncompaction of ventricular myocardium(NVM)and assess the role of MRI in the diagnosis of NVM by comparing it with echocardiography.Methods Fourteen cases of NVM diagnosed by echocardiography were examined with MRI,including scanning of black-blood sequences,double inversion recovery fast spin echo (DIRFSE)and triple inversion recovery fast spin echo(TIRFSE),and white blood sequence:fast imaging employ steady state acquisition(FIESTA).Scanning plane includes short axis view,four-chamber view and long axis view.Results Both MRI and echocardiography displayed involvement of left ventricles in thirteen cases and involvement of double ventricles in one case.Apexes of heart and the intermedius are commonly affected.MRI showed 54 segments and echocardiography showed 53 segments affected,and there is no significant difference between the capability of MRI and echocardiography(P=1.000).The affected myocardium consisted of two layers:subendoeardial noncompacted myocardium and epicardial compacted myocardium,and the ratio measurement of N/C by MRI was 3.37?0.89 and it was 3.19?0.82 by echocardiography.Noncompacted myocardium was characterized by prominent and excessive myocardial trabeculations and deep intratrabecular recesses,in which the blood flow was communicated with the ventricle.One case was complicated with ventricular aneurysm,and coronary arteriography was performed with unremarkable findings.One case underwent heart transplantation because of progressive heart failure, Gross findings demonstrated prominent muscular trabeculations with deep intratrabecular recesses,which coincided well with MRI findings.Conclusion The MRI manifestation of NVM is characteristic,and MRI with multiple series and planes is helpful in the diagnose of NVM.Compared with echoeardiography,MRI could display the pathological cardiac muscle more clearly,because of its high soft-tissue resolution and spatial resolution.
4.Performance test and evaluation on Halcyon medical linear accelerator
PENG Jun zhe ZHAI He zheng CHEN Dong hui ZHAI Zi po LONG Hui jia CHENG Yan meng
China Occupational Medicine 2022;52(04):458-
Abstract: Objective
To evaluate the key quality control and protective performance test of Halcyon medical linear accelerator.
Methods WS 674-2020Specification for Testing of Quality Control in Medical Linear Accelerator(
According to the hereinafter
WS 674-2020) ,
referred to and the manufacturer´s manual the performance of the first Halcyon medical linear accelerator in
Results , ,
Hunan Province was tested. The results showed that all ten indicators of the accelerator including dose deviation
, , ( , , , -
repeatability linearity daily stability and symmetry the results were 0.10% 0.03% 0.04% 0.50% and 100.50% 100.80%
), - -
respectively met the requirements of WS 674 2020. The results of manufacturer quality control indicators such as dose rate
, ,
stability in beam gantry rotation isocenter and mechanical position accuracy megavolt image parameters and cone beam
computer tomography image parameters met the requirements of the manufacturer´s regulations. Due to the special structure and
, - :
function of the accelerator it is difficult to detect the parameter required by WS 674 2020 as below the radiation leakage
- , , , ,
outside the M zone the uniformity the indicators related to the light field the offset of the radiation beam axis the zero scale
Conclusion -
position of the rotating motion scale and others. It is difficult to carry out complete testing according to WS 6742020
for Halcyon medical linear accelerator and it is urgent for the state to issue relevant testing standards to standardize and
strengthen the quality control testing of various accelerators.
5.Application of calcium ionophore A23187 in ICSI for globozoospermia: A report of 2 cases and review of the literature.
Hui-jun YANG ; Mei LI ; Shui-ying MA ; Cheng LI ; Yuan-yuan FAN ; Jiao-jing LIU ; Zi-jiang CHEN
National Journal of Andrology 2015;21(4):338-341
OBJECTIVETo investigate the pathogenesis of globozoospermia, fertilization ability of round-headed sperm, and the application value of assisted oocyte activation in intracytoplasmic sperm injection (ICSI) for the wives of glohozoospermia men.
METHODSWe collected oocytes from the wives of 2 globozoospermia patients and randomly divided them into two groups after ICSI to receive calcium ionophore A23187-activation and conventional treatment, respectively. We reviewed the relevant literature published at home and abroad, and discussed the etiology of globozoospermia, fertilization ability of round-headed sperm, and treatment options for this disease.
RESULTSQuality embryos were obtained in the A23187-activation group while no fertilized oocytes, oocyte cleavage, quality embryos, or blastular formation were found in the conventional treatment group. Both women achieved pregnancy and gave birth to healthy neonates after transfer of the quality embryos from the A23187-activation group.
CONCLUSIONCalcium ionophore A23187 can be applied to ICSI for the wives of globozoospermia men and bring about desirable clinical outcomes. Meanwhile, attention should be paid to its safety.
Calcimycin ; therapeutic use ; Calcium Ionophores ; therapeutic use ; Female ; Humans ; Infertility, Male ; drug therapy ; Male ; Oocytes ; Pregnancy ; Sperm Injections, Intracytoplasmic ; Spermatozoa ; abnormalities
6.A qualitative study on the change of practice of ICU advanced practice nurses be-fore and after training program
Chinese Journal of Nursing 2017;52(12):1427-1431
Objective To describe the change of practice of ICU advanced practice nurses after attending ICU Clinical Nurse Specialist(CNS) training program in Shanghai. Methods A purposive sampling method was used to recruit 15 ICU advanced practice nurses and semi-structured interviews were conducted. Thematic analysis was used for data analysis. Results Four themes regarding practice change were extracted,including extension of scope of practice,transformation of emphasis in work,promotion of clinical reforms and improvement of self-development. Conclusion The practice of ICU advanced practice nurses has changed after training,while the degree of change varies in different themes. Further quantitative researches should be conducted to provide more information for the development of ICU advanced practice nurses.
7.Development of duplex TaqMan PCR assay for detection of specific gene sequence from Bacillus anthracis
Shi-Kui WANG ; Ji-Hong HU ; Ming HOU ; Cheng GONG ; Zi-Yu SHEN ; Hui GUO ; Jian-Ping CAI ;
Chinese Journal of Laboratory Medicine 2003;0(09):-
Objective To establish a rapid assay with high sensitivity and specificity based on the sequences for group specific gene (GS) and pathogenicity island pag A gene.Methods The PCR primers and probes were designed after the whole sequence was systemically analyzed with bio-informafion tools and blasted with Genebank database.The amplicons were inserted into plasmids so that they could be used as the standard templates to evaluate the sensitivity of the diagnostic system.This assay was based on TaqMan probes and portable Smartcycle PCR machine.Results The detection level was approximately 100 copies per reaction.There was no cross-reaction with other species of Bacillus.This assay could be completed in one hour in laboratory.Conclusion The duplex TaqMan PCR assay could be used to detect Bacillus anthracis rapidly with high sensitivity and specificity.
8.Association of schizophrenia with a promoter polymorphism in the dopamine D2 receptor gene.
Dai-hui PENG ; Gao-hua WANG ; Zi-li CHENG ; De-xin ZHANG ; Kai-da JIANG
Chinese Journal of Medical Genetics 2005;22(1):94-95
OBJECTIVETo investigate the association of -141C insert/delete polymorphism with schizophrenia in Wuhan of Hubei province.
METHODSA case-control study was conducted to analyze the polymorphism in the D(2) receptor gene promoter region with schizophrenia. A total of 120 cases of schizophrenia diagnosed according to CCMD-II R criteria and 100 normal controls were recruited in the study.
RESULTSIn this sample, the allele and genotype showed statistically significant differences between patients and normal controls (P<0.05).Especially, the frequency of -141C del was 11% in patients and 18% in control(OR 0.55, 95% CI 0.30-0.96; P<0.05). This allele was less common in schizophrenia than in normal controls (P<0.05).
CONCLUSIONThe -141C del polymorphism is associated with schizophrenia.The polymorphism may modify the association with other factors. Possibly -141C del in the DRD(2) promoter region is a strong candidate for a protective factor for this trait.
Adult ; Alleles ; Female ; Gene Frequency ; Genotype ; Humans ; Male ; Middle Aged ; Polymerase Chain Reaction ; Polymorphism, Genetic ; Promoter Regions, Genetic ; genetics ; Receptors, Dopamine D2 ; genetics ; Schizophrenia ; diagnosis ; genetics
9.Expression of matrix metalloproteinase-9 in myocardium of mice with viral myocarditis.
Min YANG ; Chun-Yuan CHEN ; Zi-Li CAI ; Bo-Lin CHEN ; Liang CHENG ; Hui LI
Chinese Journal of Contemporary Pediatrics 2011;13(8):669-673
OBJECTIVETo investigate the dynamic changes of expression of matrix metalloproteinases-9 in myocardium of mice with viral myocarditis (VMC) and its significance in the pathogenesis of viral myocarditis.
METHODSVMC model was prepared by an injection of CVB3 in BALB/C mice. The mice receiving an injection of culture solution without virus were used as the control group. Cardiac tissues were obtained 7, 14, 21 and 28 days after injection and made into paraffin sections. Myocardial histopathologic changes were observed by hematoxylin-eosin staining and Masson staining. The expression of MMP-9, type I collagen and type III collagen in cardiac tissues were quantified by SABC immunohistochemical method.
RESULTSThe expression of MMP-9 in the VMC model group was observed on the 7th day, reached a peak on the 14th day, and was significantly higher than that in the control group at all time points (P<0.05). Compared with the control group, the expression of type I collagen in the VMC model group was up-regulated on the 21st day and reached a peak on the 28th day (P<0.05). The expression of type III collagen in the VMC model group was significantly higher than that in the control group on the 28th day (P<0.05). The expression of MMP-9 was positively correlated with myocardial histopathologic scores (r=0.832, P<0.05) and negatively correlated with type I collagen expression (r=-0.791, P<0.05).
CONCLUSIONSMMP-9 is over-expressed at the early stage in VMC mice, and participates in the pathological process of VMC through mediating the degradation metabolism of type I collagen. It may be an important factor that leads to myocardial collagen remodeling and myocardial fibrosis.
Animals ; Collagen Type I ; analysis ; Collagen Type III ; analysis ; Coxsackievirus Infections ; enzymology ; Enterovirus B, Human ; Immunohistochemistry ; Male ; Matrix Metalloproteinase 9 ; analysis ; Mice ; Mice, Inbred BALB C ; Myocarditis ; enzymology ; pathology ; Myocardium ; enzymology ; pathology
10.Construction and selection of the most efficient siRNA interfering plasmid specific to mouse Qa-1 gene.
Zi-He CHENG ; Jian-Pei FANG ; Hong-Gui XU ; Qiu-Hui PAN
Journal of Experimental Hematology 2008;16(5):1170-1173
This study was purposed to construct three siRNA eukaryotic expression vector specific to mouse Qa-1 gene, to investigate its silencing effect on Qa-1 gene and to select the most efficient siRNA plasmid specific to mouse Qa-1 gene. Three siRNA peptides specific to mouse Qa-1 through siRNA Web design tools of Ambion company were chosed. Jingsai Company helped to complete the siRNA eukaryotic expression vector. The mouse NIH3T3 cells cultured in RPMI 1640 medium with 10% fetal bovine serum were divided into four groups: three groups of the cells were transfected with lipofectamine 2000 reagent and three different siRNA eukaryotic expression vectors, while one group cells were transfected with lipofectamine 2000 reagent alone as negative control. Cells were collected at 24, 48, 72 hours after transfection; the RNA level of Qa-1 was detected by RT-PCR, and the expression position was examined with flow cytometry analysis by using anti-Qa-1 monoclonal antibody. The results indicated that the constructed three siRNA eukaryotic expression vectors were found to be specific to mouse Qa-1 gene. The sequence analysis showed that the sequence was identical to what chosed from web tools. NIH3T3 cells in vitro were adhered in culture that cell shape appeared to change after transfection. RT-PCR and flow cytometry analysis by using anti-Qa-1 monoclonal antibody approved that both Qa-1 RNA and the expression of Qa-1 on cell surface decreased. The decreased levels in the three groups were different. At 24, 48 and 72 hours, the expression of Qa-1 on NIH3T3 cells decreased as in the following: H2-T231: 60.9%, 81.9%, 43.6%; H2-T232: 64.5%, 73.9%, 61.1%; H2-T233: 61.9%, 71.2%, 47.5%. H2-T232 was most efficient one in all three time points. It is concluded that all three siRNA eukaryotic expression vectors selected can successfully suppress the expression of the Qa-1, and from them H2-T232 is most efficient.
Animals
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Base Sequence
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Cells, Cultured
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Gene Silencing
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Genetic Vectors
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Histocompatibility Antigens Class I
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genetics
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Mice
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NIH 3T3 Cells
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Plasmids
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RNA, Small Interfering
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genetics
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Transfection