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甲状腺癌患者组织miR表达的变化探究
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作者 徐雪瑶 《中国医药指南》 2020年第3期22-22,共1页
目的探究与观察甲状腺癌患者组织miR表达的变化情况。方法选取2016年1月至2017年11月本院就诊的52例甲状腺癌患者为观察组,同时期的52例甲状腺良性疾病患者为对照组。检测与比较两组的组织miR表达情况,并比较不同分期甲状腺癌患者的组织... 目的探究与观察甲状腺癌患者组织miR表达的变化情况。方法选取2016年1月至2017年11月本院就诊的52例甲状腺癌患者为观察组,同时期的52例甲状腺良性疾病患者为对照组。检测与比较两组的组织miR表达情况,并比较不同分期甲状腺癌患者的组织miR表达情况。结果观察组的组织miR表达高于对照组,分期较高的甲状腺癌患者的组织miR表达高于分期较低者,差异有统计学意义(P<0.05)。结论甲状腺癌患者的组织miR呈现高表达的情况,且分期较高者的表达也相对较高,因此在甲状腺癌患者中的检测价值较高。 展开更多
关键词 甲状腺癌 组织 mir表达
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化瘀散结方对晚期非小细胞肺癌患者CEA、CYFRA211、miR及MMP表达的影响 被引量:17
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作者 段铮 周庆伟 孙宏新 《辽宁中医杂志》 CAS 2020年第1期89-92,共4页
目的研究化瘀散结方对晚期非小细胞肺癌患者癌胚抗原(CEA)、细胞角蛋白19片段(CYFRA21-1)、miR及基质金属蛋白酶(MMP)表达的影响。方法以2015年10月—2017年11月本院收治的70例晚期非小细胞肺癌患者作对象,按电脑数字表法随机分组,每组... 目的研究化瘀散结方对晚期非小细胞肺癌患者癌胚抗原(CEA)、细胞角蛋白19片段(CYFRA21-1)、miR及基质金属蛋白酶(MMP)表达的影响。方法以2015年10月—2017年11月本院收治的70例晚期非小细胞肺癌患者作对象,按电脑数字表法随机分组,每组各35例,对照组施予常规化疗,实验组于此基础施予化瘀散结方治疗,对比分析两组患者CEA、CYFRA21-1、miR及MMP表达。结果治疗后,实验组CEA是(20.05±4.29)ng/m L,比对照组(26.29±5.27)ng/m L低,且实验组CYFRA21-1是(3.10±2.07)ng/m L,比对照组(4.27±2.10)ng/m L低,差异有统计学意义(P<0.05);实验组miR-21、miR-31及miR-155表达均比对照组低,差异有统计学意义(P<0.05);实验组MMP-2、MMP-9及MMP-11表达也比对照组低,差异有统计学意义(P<0.05)。结论化瘀散结方治疗晚期非小细胞肺癌有助于改善患者CEA、CYFRA211、miR及MMP表达,值得推广。 展开更多
关键词 化瘀散结方 晚期非小细胞肺癌 癌胚抗原 细胞角蛋白19片段 mir表达 基质金属蛋白酶
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Construction and Preliminary Identification of Eukaryotic Expression Vector of Cryptosporidium parvum miR-2980
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作者 呼高伟 程天印 +5 位作者 米荣升 秦培兰 黄燕 周鹏 曹薇 陈兆国 《Agricultural Science & Technology》 CAS 2012年第5期1093-1096,共4页
[Objective] This study aimed to construct and preliminarily identify the eu- karyotic expression vector of Cryptosporidium parvum miR-2980. [Method] The cp-miR- 2980 precursor was amplified from C. parvum genomic DNA ... [Objective] This study aimed to construct and preliminarily identify the eu- karyotic expression vector of Cryptosporidium parvum miR-2980. [Method] The cp-miR- 2980 precursor was amplified from C. parvum genomic DNA and cloned into pMD18- T vector. The amplified precursor was then subcloned into pVAX I vector and identi- fied with restriction endonuclease digestion and sequencing. The recombinant plasmid pVAX-miR2980 was transfected into HCT-8 cells. Total RNA was extracted and the expression of cp-miR-2980 was evaluated by RT-PCR detection. [Result] The results showed that the recombinant eukaryotic expression vector pVAX-miR2980 was suc- cessfully constructed, which can express cp-miR-2980 in HCT-8 cell. [Conclusion] This study laid the foundation for further exploring the biological function of cp-miR-2980. 展开更多
关键词 cp-mir-2980 PRECURSOR Eukaryotic expression vector RT-PCR
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Overlapping expression of microRNAs in human embryonic colon and colorectal cancer 被引量:32
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作者 Mariano Monzo Alfons Navarro +10 位作者 Eva Bandres Rosa Artells Isabel Moreno Bemat Gel Rafael Ibeas Jose Moreno Francisco Martinez Tania Diaz Antonio Martinez Olga Balague Jesus Garcia-Foncillas 《Cell Research》 SCIE CAS CSCD 2008年第8期823-833,共11页
MicroRNAs (miRNAs) are essential for regulating cell differentiation and maintaining the pluripotent state of stem cells. Although dysregulation of specific miRNAs has been associated with certain types of cancer, t... MicroRNAs (miRNAs) are essential for regulating cell differentiation and maintaining the pluripotent state of stem cells. Although dysregulation of specific miRNAs has been associated with certain types of cancer, to date no evidence has linked miRNA expression in embryonic and tumor tissues. We assessed the expression of mature miRNAs in human embryonic colon tissue, and in colorectal cancer and paired normal colon tissue. Overlapping miRNA expression was detected between embryonic colonic mucosa and colorectal cancer. We have found that the miR-17-92 cluster and its target, E2F1, exhibit a similar pattern of expression in human colon development and colonic carcinogenesis, regulating cell proliferation in both cases. In situ hybridization confirmed the high level of expression of miR-17-5p in the crypt progenitor compartment. We conclude that miRNA pathways play a major role in both embryonic development and neoplastic transformation of the colonic epithelium. 展开更多
关键词 mirNA colorectal cancer development mirNA in situ hybridization mir-17-5p cluster mir-17-92
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