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Analysis of circulating microRNA biomarkers for breast cancer detection: a meta-analysis.

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      Abstract

      Circulating microRNAs (miRNAs) have been reported to be aberrantly expressed in patients with breast cancer (BC) and thus may serve as potential diagnostic biomarkers. This meta-analysis aimed to assess the potential diagnostic value of using circulating miRNAs for BC. The summary receiver operator characteristic (SROC) curve was used to assess the overall diagnostic performance of circulating miRNA. All analyses were performed using STATA 12.0 software. Thirty-one studies from 16 publications with a total of 1,668 BC patients and 1,111 healthy controls were included in this meta-analysis. Our results showed that the pooled sensitivity (SEN) for miRNAs assays was 0.77 (95 % CI 0.69-0.84), specificity (SPE) was 0.88 (95 % CI 0.79-0.93), positive likelihood ratio (PLR) was 4.2 (95 % CI 3.0-6.0), negative LR (NLR) was 0.29 (95 % CI 0.21-0.40), and diagnostic odds ratio (DOR) was 18 (95 % CI 10-32). The area under the SROC curve (AUC) was 0.89 (95 % CI 0.86-0.91). Subgroup analysis suggested that employing a combination of multiple miRNAs was better than using a single miRNA in SEN (0.88 vs. 0.69), SPE (0.88 vs. 0.89), PLR (6.3 vs. 3.3), NLR (0.14 vs. 0.41), DOR (48 vs. 10), and AUC (0.94 vs. 0.83). In conclusion, our meta-analysis suggested that the expression profiles of circulating miRNAs, especially using a combination of them, have potential to facilitate accurate breast tumor detection. However, there are still challenges that need to be addressed to establish these new biomarkers before they can be applied to routine clinical procedures.

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      Author and article information

      Affiliations
      [1 ] Institute of Hospital Management and Research, Chinese PLA General Hospital, Beijing, 100853, China, liulihua_pla@yeah.net.
      Journal
      Tumour Biol.
      Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine
      Springer Nature
      1423-0380
      1010-4283
      Dec 2014
      : 35
      : 12
      25195131
      10.1007/s13277-014-2533-5

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