共查询到19条相似文献,搜索用时 218 毫秒
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目的分析血清中miR-155的表达水平,探讨其与乳腺癌临床病理特征之间的关系。方法收集2010年12月至2011年4月入院的67例女性患者(乳腺癌45例,非乳腺癌22例)的血液标本,分离血清并提取miRNA,通过荧光实时定量PCR法检测血清中miR-155的表达水平,分析其与乳腺癌临床病理特征间的相关性。结果乳腺癌患者相比非乳腺癌患者,腋窝淋巴结转移阳性乳腺癌患者相比阴性患者血清中miR-155表达水平均上调(均P〈0.05);在乳腺癌患者中,肿瘤大小为T1的相比T2和r乃患者,I、Ⅱ期相比Ⅲ期患者,ER、PR阳性相比阴性患者血清中的miR-155表达水平均下调(均P〈0.05)。结论血清中miR.155的表达水平与乳腺癌及其临床病理特征密切相关。miR-155可成为新-代的乳腺癌标志物,并为乳腺癌发病机制及治疗和预后判断研究提供-个新方向。 相似文献
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摘 要:[目的] 研究结肠癌患者血浆、组织中小分子非编码RNA (microRNA,miRNA) 100/200c表达水平与临床病理的相关性。[方法] 用实时定量PCR方法测定确诊为结肠癌的80例患者血浆miRNA 100、结肠癌组织中miRNA 200c表达水平并与其在正常人群血浆及癌旁正常组织中的表达进行比较。[结果] 结肠癌患者血浆中miRNA 100的表达水平显著性低于正常人群(P=0.014),结肠癌组织中miRNA 200c表达量显著性低于癌旁正常组织(P=0.0002);结肠癌患者血浆中miRNA 100相对表达量与肿瘤分化程度、发生转移、临床分期显著性相关(P<0.05),且miRNA 100表达高低与患者的肿瘤直径,临床分期、淋巴结转移相关(P<0.05);结肠癌组织中miRNA 200c表达量与发生转移、临床分期显著性相关(P<0.05),miRNA2000表达高低与肿瘤直径大小相关(P<0.05)。[结论] 与在正常组织或血浆中相比,miRNA 100/200c在结肠癌中表达量降低,与肿瘤远处转移、淋巴结转移、临床分期等病理参数密切相关。 相似文献
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乳腺癌端粒酶活性及多项生物学指标表达与临床相关性分析研究 总被引:1,自引:0,他引:1
目的研究乳腺癌组织中端粒酶活性的表达,探讨端粒酶活性与ER、PR、CerbB-2、PCNA及Cath-D的相关性,分析其与乳腺癌肿瘤大小、临床分期、病理组织学分型及淋巴结转移的关系.方法采用PCR-ELISA法和免疫组化技术,检测乳腺癌组织中的端粒酶活性,ER、PR、CerbB-2、PCNA及Cath-D的蛋白表达水平.结果在乳腺癌组织中端粒酶活性、ER、PR、CerbB-2、PCNA及Cath-D阳性表达率分别为82.0%、67.5%、65.0%、65.0%、77.5%、52.5%.端粒酶活性与乳腺癌肿瘤大小、临床分期、淋巴结转移有相关性,与病理组织学分型无相关性.端粒酶活性与ER有相关性,与PR、CerbB-2、PCNA 、Cath-D的表达无相关性.结论端粒酶活性与ER水平、肿瘤大小、临床分期、淋巴结转移有相关性,可作为评估乳腺癌预后的分子生物学指标. 相似文献
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MicroRNAs and their target gene networks in breast cancer 总被引:1,自引:0,他引:1
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The purpose of this study was to identify and validate circulating microRNAs (miRNAs) in human plasma for use as breast cancer (BC) biomarkers and to analyze their relationship to clinicopathologic features and its preliminary biological function. Genome-wide expression profiling of miRNAs in BC was investigated by microarray analysis. miR-155 was up-regulated greater than two-fold in BC compared with Normal Adjacent Tissue (NAT), whereas let-7b, miR-381, miR-10b, miR-125a-5p, miR-335, miR-205 and miR-145 were down- regulated greater than two-fold. Our hypothesis was that circulating miRNAs are also present and differentially expressed in the serum of BC patients compared to controls. Using real-time PCR (RT-PCR), we analyzed miR-205 and miR-155 in archived serum from 30 participants, 20 with breast cancer and 10 healthy people. miR-205 was down-regulated in BC patient serum while miR-155 was up-regulated. Furthermore, we analyzed the relationship between the expression levels of these two miRNAs and the clinicopathologic parameters of BC patients. High expression of miR155 was associated with clinical stage, molecular type, Ki-67 and p53 in BC patients (P<0.05). By contrast, we found no significant correlation between miR-205 and BC patient clinicopathologic parameters. Functional analysis showed that ectopic expression of miR-205 significantly inhibits cell proliferation and promotes apoptosis. miR-205 was down-regulated and miR-155 was up-regulated in BC patient serum. miR-155 was positive correlated with clinical stage and ki-67 and negatively correlated with p53 status. 相似文献
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Wang G Chan ES Kwan BC Li PK Yip SK Szeto CC Ng CF 《Clinical genitourinary cancer》2012,10(2):106-113
BackgroundMicroRNAs (miRNA) have been implicated to play an important role in the pathogenesis of a variety of cancers. We studied the levels of miRNAs related to epithelial-mesenchymal transition (EMT) in the urine of patients with bladder cancer.MethodThe expression of the miR-200 family, miR-205, miR-192, miR-155, and miR-146a in the urine sediment and supernatant of 51 patients with bladder cancer and in 24 controls was determined by real-time quantitative polymerase chain reaction.ResultsCompared with controls, the patients with bladder cancer had a lower expression of the miR-200 family, miR-192, and miR-155 in the urinary sediment; lower expression of miR-192; and higher expression of miR-155 in the urinary supernatant. The expression of the miR-200 family, miR-205, and miR-192 in the urine sediment significantly correlated with urinary expression of EMT markers, including zinc finger E-box-binding homeobox 1, vimentin, transforming growth factor β1, and Ras homolog gene family, member A. Furthermore, the levels of miR-200c and miR-141 in the urine sediment became normalized after surgery.ConclusionWe found that the urinary miR-200 family, miR-155, miR-192, and miR-205 levels are depressed in patients with bladder cancer. The level of these miRNA targets in urine has the potential to be developed as noninvasive markers for bladder cancer. 相似文献
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Plasma Circulating Mirnas Profiling for Identification of Potential Breast Cancer Early Detection Biomarkers 下载免费PDF全文
A Rashid JusohSivanesan Vijaya MohanTan Lu PingTengku Ahmad Damitri Al Astani Bin Tengku DinJuhara Haron Roslini Che RomliHasnan JaafarSiti Norasikin NafiTuan Ismail Tuan SalwaniMaya Mazuwin Yahya 《Asian Pacific journal of cancer prevention》2021,22(5):1375-1381
Objective: This study aimed to characterize the miRNA expression profiles from plasma samples of our local breast cancer patients in comparison to healthy control by using miRNA PCR Array. Methods: In this study, plasma miRNA profiles from eight early-stage breast cancer patients and nine age-matched (± 2 years) healthy controls were characterized by miRNA array-based approach, followed by differential gene expression analysis, Independent T-test and construction of Receiver Operating Characteristic (ROC) curve to determine the capability of the assays to discriminate between breast cancer and the healthy control. Results: Based on the 372-miRNAs microarray profiling, a set of 40 differential miRNAs was extracted regarding to the fold change value at 2 and above. We further sub grouped 40 miRNAs of breast cancer patients that were significantly expressed at 2-fold change and higher. In this set, we discovered that 24 miRNAs were significantly upregulated and 16 miRNAs were significantly downregulated in breast cancer patients, as compared to the miRNA expression of healthy subjects. ROC curve analysis revealed that seven miRNAs (miR-125b-5p, miR-142-3p, miR-145-5p, miR-193a-5p, miR-27b-3p, miR-22-5p and miR-423-5p) had area under curve (AUC) value > 0.7 (AUC p-value < 0.05). Overlapping findings from differential gene expression analysis, ROC analysis, and Independent T-Test resulted in three miRNAs (miR-27b-3p, miR-22-5p, miR-145-5p). Cohen’s effect size for these three miRNAs was large with d value are more than 0.95. Conclusion: miR-27b-3p, miR-22-5p, miR-145-5p could be potential biomarkers to distinguish breast cancer patients from healthy controls. A validation study for these three miRNAs in an external set of samples is ongoing. 相似文献
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Zheng SR Guo GL Zhang W Huang GL Hu XQ Zhu J Huang QD You J Zhang XH 《Oncology reports》2012,27(4):1149-1155
Accumulating evidence shows that mircroRNAs (miRNAs) play a vital role in tumorigenesis. miR-155 is one of the most multifunctional miRNAs whose overexpression has been found to be associated with different types of cancer including breast cancer. To further determine the potential involvement of miR-155 in breast cancer, we evaluated the expression levels of miR-155 by real-time PCR and correlated the results with clinicopathological features. Matched non-tumor and tumor tissues of 42 infiltrating ductal carcinomas and 3 infiltrating lobular carcinomas were analyzed for miR-155 expression by real-time PCR. Further, we used an antisense technique to inhibit miR-155 expression in vitro. WST-8 test was performed to evaluate cell viability and apoptosis assay was used to investigate the effect of the miR-155 antisense oligonucleotide (miR-155 ASO) on HS578T cell death. The expression levels of miR-155 were significantly higher in tumor tissues than the levels in matched non-tumor tissues (P<0.001). Up-regulated miR-155 expression was associated with lymph node positivity (P=0.034), higher proliferation index (Ki-67 >10%) (P=0.019) and advanced breast cancer TNM clinical stage (P=0.002). Interestingly, we next found that miR-155 expression levels had close relations with ER status (P=0.041) and PR status (P=0.029). Transfection efficiency detected by flow cytometry was higher than 70%, the WST-8 test showed that viability of HS578T cells was greatly reduced after transfection with miR-155 ASO compared with the scramble (SCR) group or the liposome group. The Annexin V-FITC/PI assay also indicated that transfection with miR-155 ASO promoted apoptosis. 相似文献
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