1.A meta analysis of influence of patellar resurfacing on effect of total knee arthroplasty
Xuanming LI ; Quanxing LIU ; Shiwen ZHANG
Chongqing Medicine 2016;45(33):4680-4683
Objective To evaluate the influence of patellar resurfacing and non-patellar resurfacing on the effect of total knee arthroplasty to provide the evidence-based basis for selecting the clinical treatment scheme.Methods The clinical randomized controlled trials(RCT)on the whether having patellar replacement in total knee arthroplasty were retrieved from the databases of Pubmed,Cochrane,Medline,Embase,CNKI and WanFang data.The screening was independently performed by two researchers according to the including and excluding criterion.The related data were extracted.The reoperation rate,knee joint pain score and knee joint score served as the measurement criteria.The RevMan 5.2 software was adopted to conduct the meta analysis.Results Fifteen literatures were included to analyze,involving 1 788 patients,among them 871 cases were in the patellar resurfacing group and 917 case sin the non-patellar resurfacing group.The reoperation rate in the patellar resurfacing group was significantly lower than that in the non-patellar resurfacing group(RR=0.50,95 %CI:0.33-0.76;P =0.001),moreover the knee joint function was significantly improved(WMD=3.04,95%CI:0.41-5.67;P=0.02).However,the anterior knee joint pain(WMD=0.96,95%CI:-0.85-2.76;P=0.30)and knee joint score(RR=0.81,95 % CI:0.50-1.32;P =0.41) had no statistical difference between the two operation modes.Conclusion Conducting patellar resurfacing in total knee arthroplasty can reduce the reoperation risk and improves the postoperative knee joint function,but does not improve postoperative knee joint pain score and knee joint score
2.Genetic diversity of 12 species of germplasm resources for Potentilla discolor based on ISSR analysis
Yueji LUO ; Xianjin WU ; Shuai PENG ; Xuanming LIU
Chinese Traditional and Herbal Drugs 1994;0(05):-
Objective To study the genetic diversity of germplasm resources for Potentilla discolor.Methods Twelve species of germplasm resources for P.discolor were analyzed by ISSR molecular markers.To make up the systematic diagram of genetic relationship by POPGENE 1.32 software,cluster by UPGMA method,and establish the dendrogram.Results A total of 128 ISSR bands were scored for 12 primers,among which 101 were polymorphic bands.The average percentage of polymorphic bands was 78.91%.Genetic similarity coefficient was changed from 0.179 2 to 0.632 5.By cluster analysis,the geographical distribution is mutually related to the relationship of germplasm resources for P.discolor and it was also showed some of P.discolor from the same region were in the same group which presented the rule of geographical distribution in the tested materials.Conclusion The diversity level of the different germplasm resources for P.discolor higher and the relationship of P.discolor correlates with the geographical location in some way.
3.SACSR:a low power BIST method for sequential circuits
Shaochong LEI ; Jun GUO ; Lei CAO ; Zeye LIU ; Xuanming WANG
Journal of Pharmaceutical Analysis 2008;20(3):155-159
A novel built-in-self-test (BIST) method called seeded autonomous cyclic shift register (SACSR) is presented to reduce test power of the sequential circuit. The key idea is to use a pseudorandom pattern generator and several XOR gates to generate seeds that share fewer test vectors. The generated seed is taken XOR operation with a cyclic shift register, and the single input change (SIC) sequence is generated. The proposed scheme is easily implemented and can reduce the switching activities of the circuit under test (CUT) greatly. Experimental results on ISCAS89 benchmarks show that on average more than 63% power reduction can be achieved. It also demonstrates that the generated test vectors attain high fault coverage for stuck-at fault and transition fault coverage with short test length.
4.Influence of DNAzymes against cyclin D1 in tumor cell cycle.
Dan LI ; Junyi ZHU ; Yayan ZHOU ; Xuanming LIU
Journal of Biomedical Engineering 2009;26(2):374-384
In this study, DNAzymes against cyclin D1 (cyclin D1-DRz) were designed according to the secondary structure of cyclin D1 mRNA which was computed with RNAdraw and Mfold. Cyclin D1-DRz were transfected into tumor cell line u251 and HeLa by oligofectamine. The expression of cyclin D1 was detected by RT-PCR. It was shown that the expression of cyclin D1 gene was suppressed obviously, and the expressions of other cell-cycle related genes such as cyclin E1, cyclin A1 and cyclin B1 were also declined. The cell cycle analysis of tumor cells tansfected with cyclin D1-DRz revealed an arrestment in the G0/G1 phase. In conclusion, the approach is effective and feasible for designing DNAzyme. Cyclin D1-DRz is useful for interfering with the cell cycle procession of tumor cells.
Base Sequence
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Cell Cycle
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drug effects
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Cyclin D1
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antagonists & inhibitors
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genetics
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metabolism
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DNA, Catalytic
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genetics
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metabolism
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pharmacology
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HeLa Cells
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Humans
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Molecular Sequence Data
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RNA, Messenger
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genetics
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metabolism
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Transfection
5.Experimental study of inhibition of tumor cell proliferation by a novel gene SPATA12.
Zhiwen LIU ; Yiting LIN ; Xuanming LIU ; Weiwei YU ; Yunsheng ZHANG ; Dan LI
Journal of Central South University(Medical Sciences) 2012;37(3):222-227
OBJECTIVE:
To explore the inhibitory role of spermatogenesis-associated gene 12 (SPATA12) on tumor cell proliferation and its possible mechanism.
METHODS:
The expression pattern of SPATA12 in testicular tumors was investigated by in situ hybridization analysis using tissue microarrays. The effects of SPATA12 on tumor cell proliferation and colony formation was detected by 3-(4.5-dimethylthiazol-2- yl)-2,5-diphenyl tetrazolium bromide (MTT) assay and colonyforming assays, respectively. The changes of expression level of cell cycle genes in tumor cells were detected by reverse transcription polymerase chain reaction(RTPCR).
RESULTS:
In situ hybridization analysis showed that the SPATA12 was highly expressed in normal adult testis, but lacking in testicular tumors such as seminoma. MTT assay and colony-forming assay indicated that the exogenous expression of SPATA12 could suppress both tumor cell proliferation and colony formation. RT-PCR showed that the expression of cyclin A1 gene was markedly suppressed and the level of cyclin D1 was somewhat reduced following SPATA12 transfection. However, no obvious changes were observed in mRNA expression of cyclin B1 or cyclin E1 after SPATA12 transfection.
CONCLUSION
SPATA12 could be an inhibitor during the development of tumor via regulation of cell cycle genes.
Cell Line, Tumor
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Cell Proliferation
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Genes, Tumor Suppressor
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Genes, cdc
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HeLa Cells
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Homeodomain Proteins
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genetics
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metabolism
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Humans
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Male
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Testicular Neoplasms
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genetics
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pathology
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Transfection