1.Progressive huge epidermoid cyst of distal femur in chronic osteomyelitis: a case report and review of literature.
Wei-Feng JI ; Pei-Jian TONG ; Zhen-Chuan MA ; Gui-Bao NI ; Gou-Hua SHEN ; Hai-Long ZHOU ; Xiao-Dong YAO ; Lu-Wei XIAO
China Journal of Orthopaedics and Traumatology 2011;24(12):1027-1029
Bone Diseases
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etiology
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surgery
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Chronic Disease
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Epidermal Cyst
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etiology
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surgery
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Femur
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Humans
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Male
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Middle Aged
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Osteomyelitis
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complications
2.Bmi-1-siRNA Regulates the Proliferation of K562 Leukemia Cells in vitro and in vivo by PTEN/pAKT Pathway.
Yu-Jiao LIU ; Kai ZHANG ; Ben LIU ; Dan-Dan LIU ; Bao-Xia ZHAO ; Xiao-Li FU ; Rong GOU ; Xiu-Xiang MENG
Journal of Experimental Hematology 2019;27(3):685-691
OBJECTIVE:
To investigate the effect of Bmi-1 gene silence on the proliferation ability of K562 cells in vitro and in vivo, and to explore the relation of molecular mechanism between proliferation ability of K562 cells in vitro and in vivo with PTEN/pAKT signaling pathway.
METHODS:
The Bmi-1 small interference RNA (siRNA) sequences were transfected into K562 cells for decreasing Bmi-1 expression. The effect of Bmi-1 siRNA on the proliferation of K562 cells in vitro and in vivo was detected by MTT method and colony-forming test, the effect of Bmi-1 siRNA on the tumorogenicity of K562 cells was observed by subcutaneous inoculation of K562 cells, LY294002 and Bpv treated K562 cells in nude mice, the expression of Bmi-1, PTEN and pAKT proteins were detected by Western blot.
RESULTS:
The Bmi-1 siRNA could inhibit the proliferation activity, colony-forming and tumor-forming abilities of K562 cells. After the silence of Bmi-1 gene, the PTEN expression in Bmi-1 gene-silenced group was significantly enhanced. While the pAKT expression in Bmi-1 gene-silenced group was significantly reduced; after the K562 cells were treated with LY294002 (an inhibitor of pAKT), the pAKT expression colony-forming and tumor forming abilities were reduced in comparison with untreated K562 cells; after the K562-S1 cells were treated with Bpv (an inhibitor of PTEN), the PTEN expression decreased, while the pAKT expression, colony forming and tumor-forming abilities were restored.
CONCLUSION
The Bmi-1 gene possibly involves in regulation of K562 proliferation in vivo and in vitro, the effect of PTEN/pAKT signaling pathway maybe one of molecular mechanisms mediating this regulation.
Animals
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Apoptosis
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Cell Proliferation
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Humans
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K562 Cells
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Leukemia
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Mice
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Mice, Nude
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PTEN Phosphohydrolase
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Polycomb Repressive Complex 1
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Proto-Oncogene Proteins c-akt
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RNA, Small Interfering
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Signal Transduction
3.Variant of Associated with Increasing Risk in Chinese Patients with Relapsing-remitting Multiple Sclerosis.
Sheng CHEN ; Juan ZHANG ; Qi-Bing LIU ; Jing-Cong ZHUANG ; Lei WU ; Yong-Feng XU ; Hong-Fu LI ; Zhi-Ying WU ; Bao-Gou XIAO
Chinese Medical Journal 2018;131(6):643-647
BackgroundMultiple sclerosis (MS) is a common central nervous system autoimmune disorder. Increasing number of genome-wide association study (GWAS) analyses hint that MS is strongly associated with genetics. Unfortunately, almost all the GWAS analyses were Caucasian population based. Numbers of risk loci might not be replicated in Chinese MS patients. Hence, we performed a MassArray Assay to genotype the previously reported variants located in the transcription regulation genes in order to elucidate their role in the Chinese MS patients.
MethodsOne hundred and forty-two relapsing-remitting MS (RRMS) patients and 301 healthy controls were consecutively collected from September 2, 2008, to June 7, 2013, as stage 1 subjects. Eight reported transcription regulation-related single-nucleotide polymorphisms (SNPs) were genotyped using the Sequenom MassArray system. In stage 2, another 44 RRMS patients and 200 healthy controls were consecutively collected and Sanger sequenced from April 7, 2015, to June 29, 2017, for the validation of positive results in stage 1. Differences in allele and genotype frequencies between patients and healthy controls, odds ratios, and 95% confidence intervals were calculated with the Chi-square test or Fisher's exact test. Hardy-Weinberg equilibrium was tested also using the Chi-square test.
ResultsIn stage 1 analysis, we confirmed only one previously reported risk variant, rs11129295 in EOMES gene. We found that the frequency of T/T genotype was much higher in MS group (χ = 10.251, P = 0.005) and the T allele of rs11129295 increased the risk of MS (χ = 10.022, P = 0.002). In stage 2 and combined analyses, the T allele of rs11129295 still increased the risk of MS (χ = 4.586, P = 0.030 and χ = 16.378, P = 5.19 × 10, respectively).
ConclusionsThis study enhances the knowledge that the variant of EOMES is associated with increasing risk in Chinese RRMS patients and provides a potential therapeutic target in RRMS.
Adolescent ; Adult ; Aged ; Alleles ; Asian Continental Ancestry Group ; Female ; Gene Frequency ; genetics ; Genetic Predisposition to Disease ; genetics ; Genome-Wide Association Study ; Genotype ; Humans ; Male ; Middle Aged ; Multiple Sclerosis ; genetics ; Odds Ratio ; Polymorphism, Single Nucleotide ; genetics ; T-Box Domain Proteins ; genetics ; Young Adult