检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
出 处:《交通医学》2016年第2期103-106,共4页Medical Journal of Communications
基 金:国家自然科学基金面上项目(21175075);江苏省医学创新团队与领军人才项目(LJ201136);南通市社会事业科技创新与示范-临床医学科技专项(HS2013067)
摘 要:目的:研究慢性髓细胞白血病(CML)患者中GFI-1的表达情况及其与BCR-ABL定量之间的关系,以探讨GFI-1在CML中的意义。方法:收集82例CML患者的骨髓标本,其中初诊慢性期50例,急变期6例,加速期6例,经伊马替尼治疗后细胞遗传学缓解期20例。以20例正常人的外周血或骨髓标本作为正常对照。应用实时定量PCR、Western blot等方法检测CML患者GFI-1、BCR-ABL的表达情况,分析两者基因表达量之间的关系。结果:(1)CML慢性期、急变期/加速期GFI-1的表达均明显高于正常对照组(P<0.05);慢性期与急变期/加速期患者GFI-1的表达差异无统计学意义(P>0.05);慢性期患者的GFI-1较缓解期表达高,差异有统计学意义(P<0.05)。(2)GFI-1与BCR-ABL定量之间成正相关(r2=0.7647,P<0.01)。结论 :CML患者GFI-1表达水平异常,可能参与CML的发生发展。Objective:Study the expression an d significance of GFI-1 in patients of chronic myeloid leukemia(CML),and evaluate the relationship of GFI-1m RNA and BCR-ABL m RNA,to explore the significance of GFI-1 in CML.Methods:Collect the bone marrow samples of 82 patients of CML which includes 50 cases of chronic phase,6 cases of CML-accelerated phase(AP),6 cases of blastic phase(BP),20 cases of Cytogenetics response by Imatinib. And 20 cases of normal peripheral blood or bone marrow samples as controls.Real-time quantitative PCR,Western blot were used to detect the expression of GFI-1、BCR-ABL in CML patients and normal,to further research the ocurrence and progress of CML.Results:(1)GFI-1 expression in CP,AP/BP in CML was significantly higher than controls(P〈0.05);expresion in CML CP and AP/BP patients was not statistically significant(P〉 0.05);CP was higher than remission expression and the difference was statistically significant(P〈0.05).(2)GFI-1m RNA expression was significantly related to BCR-ABL m RNA(r2=0.7647,P〈0.01). Conclusion: The GFI-1 expression in CML patients was significantly higher than in normal, which may be involved in the development of CML.
关 键 词:独立生长因子1 慢性髓细胞白血病 BCR-ABL融合基因
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.148