Screening circular RNA related to chemotherapeutic resistance in breast cancer

Danfeng Gao1, Xiufen Zhang1, Beibei Liu1

  • 1Oncology Institute, The Affiliated Hospital of Jiangnan University, Wuxi 214062, China.

Epigenomics
|August 15, 2017
PubMed
Abstract

Insights

Circular RNAs (circRNAs) are linked to breast cancer chemoresistance. Hsa_circ_0006528 shows potential as a therapeutic target for overcoming Adriamycin resistance in breast cancer.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genomics

Background:

  • Breast cancer remains a leading cause of cancer-related mortality worldwide.
  • Chemoresistance significantly limits the efficacy of standard breast cancer treatments.
  • Circular RNAs (circRNAs) are emerging as key regulators in various biological processes, including cancer progression and drug resistance.

Purpose of the Study:

  • To identify specific circular RNAs (circRNAs) implicated in breast cancer chemoresistance.
  • To investigate the potential role of circRNAs in Adriamycin (ADM) resistance in MCF-7 breast cancer cells.

Main Methods:

  • CircRNA expression profiling was performed using microarray analysis on ADM-resistant MCF-7 (MCF-7/ADM) and parental MCF-7 cells.
  • Differential circRNA expression was validated using quantitative real-time reverse transcription PCR (qRT-PCR).
  • Bioinformatic analyses, including TargetScan and miRanda, were employed to predict miRNA targets and gene networks of upregulated circRNAs.

Main Results:

  • A total of 3093 circRNAs were detected, with 18 circRNAs showing differential expression between MCF-7/ADM and MCF-7 cells.
  • Seven upregulated circRNAs were identified, and their potential miRNA and target gene interactions were predicted.
  • Bioinformatics analysis highlighted target genes involved in cancer-related signaling pathways.
  • The circ_0006528-miR-7-5p-Raf1 axis was identified as a potential regulatory mechanism in ADM-resistant breast cancer.

Conclusions:

  • Circular RNAs play a significant role in the development of breast cancer chemoresistance.
  • Hsa_circ_0006528 demonstrates potential as a biomarker and therapeutic target for overcoming Adriamycin resistance.
  • Further functional studies are warranted to elucidate the precise mechanisms of hsa_circ_0006528 in breast cancer chemoresistance.