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Integrated multiomic profiling of breast cancer in the Chinese population reveals patient stratification and therapeutic vulnerabilities. | LitMetric

AI Article Synopsis

  • A study was conducted on 773 Chinese breast cancer patients to address the lack of representation in large-scale molecular profiling studies and to analyze their unique biological characteristics.
  • Findings revealed that Asian patients had more targetable AKT1 mutations, a higher prevalence of the HER2-enriched subtype, and increased HER2 protein levels, suggesting a need for anti-HER2 therapy.
  • The comprehensive analysis also identified ferroptosis as a potential therapeutic target for basal-like tumors and established a method for classifying patients based on their recurrence risk, providing valuable insights for precision treatment.

Article Abstract

Molecular profiling guides precision treatment of breast cancer; however, Asian patients are underrepresented in publicly available large-scale studies. We established a comprehensive multiomics cohort of 773 Chinese patients with breast cancer and systematically analyzed their genomic, transcriptomic, proteomic, metabolomic, radiomic and digital pathology characteristics. Here we show that compared to breast cancers in white individuals, Asian individuals had more targetable AKT1 mutations. Integrated analysis revealed a higher proportion of HER2-enriched subtype and correspondingly more frequent ERBB2 amplification and higher HER2 protein abundance in the Chinese HRHER2 cohort, stressing anti-HER2 therapy for these individuals. Furthermore, comprehensive metabolomic and proteomic analyses revealed ferroptosis as a potential therapeutic target for basal-like tumors. The integration of clinical, transcriptomic, metabolomic, radiomic and pathological features allowed for efficient stratification of patients into groups with varying recurrence risks. Our study provides a public resource and new insights into the biology and ancestry specificity of breast cancer in the Asian population, offering potential for further precision treatment approaches.

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Source
http://dx.doi.org/10.1038/s43018-024-00725-0DOI Listing

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