Cancers (Apr 2021)

Development of a microRNA Panel for Classification of Abnormal Mammograms for Breast Cancer

  • Ruiyang Zou,
  • Sau Yeen Loke,
  • Veronique Kiak-Mien Tan,
  • Swee Tian Quek,
  • Pooja Jagmohan,
  • Yew Chung Tang,
  • Preetha Madhukumar,
  • Benita Kiat-Tee Tan,
  • Wei Sean Yong,
  • Yirong Sim,
  • Sue Zann Lim,
  • Eunice Png,
  • Shu Yun Sherylyn Lee,
  • Mun Yew Patrick Chan,
  • Teng Swan Juliana Ho,
  • Boon Kheng James Khoo,
  • Su Lin Jill Wong,
  • Choon Hua Thng,
  • Bee Kiang Chong,
  • Yik Ying Teo,
  • Heng-Phon Too,
  • Mikael Hartman,
  • Ngiap Chuan Tan,
  • Ern Yu Tan,
  • Soo Chin Lee,
  • Lihan Zhou,
  • Ann Siew Gek Lee

DOI
https://doi.org/10.3390/cancers13092130
Journal volume & issue
Vol. 13, no. 9
p. 2130

Abstract

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Mammography is extensively used for breast cancer screening but has high false-positive rates. Here, prospectively collected blood samples were used to identify circulating microRNA (miRNA) biomarkers to discriminate between malignant and benign breast lesions among women with abnormal mammograms. The Discovery cohort comprised 72 patients with breast cancer and 197 patients with benign breast lesions, while the Validation cohort had 73 and 196 cancer and benign cases, respectively. Absolute expression levels of 324 miRNAs were determined using RT-qPCR. miRNA biomarker panels were identified by: (1) determining differential expression between malignant and benign breast lesions, (2) focusing on top differentially expressed miRNAs, and (3) building panels from an unbiased search among all expressed miRNAs. Two-fold cross-validation incorporating a feature selection algorithm and logistic regression was performed. A six-miRNA biomarker panel identified by the third strategy, had an area under the curve (AUC) of 0.785 and 0.774 in the Discovery and Validation cohorts, respectively, and an AUC of 0.881 when differentiating between cases versus those with benign lesions or healthy individuals with normal mammograms. Biomarker panel scores increased with tumor size, stage and number of lymph nodes involved. Our work demonstrates that circulating miRNA signatures can potentially be used with mammography to differentiate between patients with malignant and benign breast lesions.

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