Plasma miR-221 as a predictive biomarker for chemoresistance in breast cancer patients who previously received neoadjuvant chemotherapy

Onkologie. 2011;34(12):675-80. doi: 10.1159/000334552. Epub 2011 Nov 23.

Abstract

Background: Neoadjuvant chemotherapy (NAC) is increasingly being used in breast cancer treatment. Research has revealed an elevated expression of miR-221 in adriamycinresistant MCF-7/ADR cells. This study aimed to explore the potential role of miR-221 as a biomarker for chemosensitivity in breast cancer patients who previously received NAC.

Patients and methods: The expression levels of circulating miR-221 in the plasma of 93 breast cancer patients who previously received NAC and in 32 healthy individuals were assessed. The correlations between miR-221 and clinicopathological features and chemosensitivity were also analysed.

Results: The expression level of miR-221 was significantly associated with hormone receptor (HR) status (p = 0.008). Patients with higher plasma miR-221 levels tended to be HR-negative. Patients with different miR-221 levels had significant differences in the overall response rate (p = 0.044) but not in the pathologic complete response rate (p = 0.477).

Conclusion: Our results indicate that plasma miR-221 may be a predictive biomarker for sensitivity to NAC in breast cancer patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anthracyclines / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Biomarkers, Tumor / blood*
  • Breast Neoplasms / blood*
  • Breast Neoplasms / diagnosis
  • Breast Neoplasms / drug therapy*
  • Bridged-Ring Compounds / therapeutic use
  • Chemotherapy, Adjuvant / statistics & numerical data
  • China / epidemiology
  • Drug Resistance, Neoplasm*
  • Female
  • Humans
  • MicroRNAs / blood*
  • Neoadjuvant Therapy / statistics & numerical data
  • Prevalence
  • Prognosis
  • Reproducibility of Results
  • Risk Assessment
  • Risk Factors
  • Sensitivity and Specificity
  • Taxoids / therapeutic use
  • Treatment Outcome

Substances

  • Anthracyclines
  • Biomarkers, Tumor
  • Bridged-Ring Compounds
  • MIRN221 microRNA, human
  • MicroRNAs
  • Taxoids
  • taxane