Characterization of the genomic landscape and actionable mutations in Chinese breast cancers by clinical sequencing

Nat Commun. 2020 Nov 10;11(1):5679. doi: 10.1038/s41467-020-19342-3.

Abstract

The remarkable advances in next-generation sequencing technology have enabled the wide usage of sequencing as a clinical tool. To promote the advance of precision oncology for breast cancer in China, here we report a large-scale prospective clinical sequencing program using the Fudan-BC panel, and comprehensively analyze the clinical and genomic characteristics of Chinese breast cancer. The mutational landscape of 1,134 breast cancers reveals that the most significant differences between Chinese and Western patients occurred in the hormone receptor positive, human epidermal growth factor receptor 2 negative breast cancer subtype. Mutations in p53 and Hippo signaling pathways are more prevalent, and 2 mutually exclusive and 9 co-occurring patterns exist among 9 oncogenic pathways in our cohort. Further preclinical investigation partially suggests that NF2 loss-of-function mutations can be sensitive to a Hippo-targeted strategy. We establish a public database (Fudan Portal) and a precision medicine knowledge base for data exchange and interpretation. Collectively, our study presents a leading approach to Chinese precision oncology treatment and reveals potentially actionable mutations in breast cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian People / genetics*
  • Biomarkers, Tumor / genetics
  • Breast Neoplasms* / genetics
  • Breast Neoplasms* / therapy
  • China
  • Data Management
  • Female
  • Genetic Markers
  • Genomics
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Molecular Targeted Therapy*
  • Mutation*
  • Neurofibromin 2 / genetics
  • Oncogenes
  • Precision Medicine
  • Prospective Studies
  • Signal Transduction / genetics
  • Tumor Suppressor Protein p53 / genetics

Substances

  • Biomarkers, Tumor
  • Genetic Markers
  • NF2 protein, human
  • Neurofibromin 2
  • Tumor Suppressor Protein p53