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微小RNA谱在Ta和T1期膀胱癌预后进展预测中的作用。

The role of microRNA profiling in prognosticating progression in Ta and T1 urinary bladder cancer.

作者信息

Segersten Ulrika, Spector Yael, Goren Yaron, Tabak Sarit, Malmström Per-Uno

机构信息

Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.

Rosetta Genomics Ltd, Rehovot, Israel.

出版信息

Urol Oncol. 2014 Jul;32(5):613-8. doi: 10.1016/j.urolonc.2013.11.001. Epub 2014 Jan 14.

Abstract

OBJECTIVE

To analyze microRNA profile in Ta and T1 urinary bladder cancers in combination and separately and to relate this to the risk of later developing higher-stage disease.

MATERIALS AND METHODS

Formalin-fixed, paraffin-embedded samples of 44 Ta and 42 T1 bladder cancers representing cases with and without stage progression during follow-up were collected and microRNA expression levels were measured by microarray analysis.

RESULTS

In a comparison between the progressors and controls, in the Ta/T1 group, miR-10a-5p and miR-31-5p were differentially expressed. miR-10a-5p was also correlated to time to progression (P = 0.00012). In the subgroup analysis, 3 microRNAs, miR-10a-5p, miR-31-5p, and miR-130a-3p, were differentially expressed among Ta tumors and had a fold change of more than 1.5 (P<0.038). The comparison concerning microRNA expression between the progressors and controls in category T1 cancers revealed no significant differences.

CONCLUSIONS

Profiling revealed that certain microRNAs predicted the risk of developing higher-stage disease among patients with Ta cancers. Lower miR-10a-5p expression in Ta progressing tumors indicates that this microRNA could be important for later malignant potential among this group of patients.

摘要

目的

联合及分别分析Ta期和T1期膀胱癌中的微小RNA谱,并将其与后期发展为更高分期疾病的风险相关联。

材料与方法

收集44例Ta期和42例T1期膀胱癌的福尔马林固定、石蜡包埋样本,这些样本代表随访期间有或无分期进展的病例,并通过微阵列分析测量微小RNA表达水平。

结果

在进展组与对照组的比较中,在Ta/T1组中,miR-10a-5p和miR-31-5p存在差异表达。miR-10a-5p也与进展时间相关(P = 0.00012)。在亚组分析中,3种微小RNA,即miR-10a-5p、miR-31-5p和miR-130a-3p,在Ta期肿瘤中存在差异表达,且倍数变化大于1.5(P<0.038)。T1期癌症进展组与对照组之间微小RNA表达的比较未发现显著差异。

结论

分析表明,某些微小RNA可预测Ta期癌症患者发展为更高分期疾病的风险。Ta期进展性肿瘤中miR-10a-5p表达较低表明,这种微小RNA可能对该组患者后期的恶性潜能具有重要意义。

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