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The nature of triple-negative breast cancer classification and antitumoral strategies

  • Kim, Songmi (Department of Nanobiomedical Science, Dankook University) ;
  • Kim, Dong Hee (Department of Anesthesiology and Pain Management, Dankook University Hospital) ;
  • Lee, Wooseok (Center for Bio-Medical Engineering Core Facility, Dankook University) ;
  • Lee, Yong-Moon (Department of Pathology, Dankook University School of Medicine) ;
  • Choi, Song-Yi (Department of Pathology, Chungnam National University School of Medicine) ;
  • Han, Kyudong (Center for Bio-Medical Engineering Core Facility, Dankook University)
  • Received : 2020.11.13
  • Accepted : 2020.12.10
  • Published : 2020.12.31

Abstract

Identifying the patterns of gene expression in breast cancers is essential to understanding their pathophysiology and developing anticancer drugs. Breast cancer is a heterogeneous disease with different subtypes determined by distinct biological features. Luminal breast cancer is characterized by a relatively high expression of estrogen receptor (ER) and progesterone receptor (PR) genes, which are expressed in breast luminal cells. In ~25% of invasive breast cancers, human epidermal growth factor receptor 2 (HER2) is overexpressed; these cancers are categorized as the HER2 type. Triple-negative breast cancer (TNBC), in which the cancer cells do not express ER/PR or HER2, shows highly aggressive clinical outcomes. TNBC can be further classified into specific subtypes according to genomic mutations and cancer immunogenicity. Herein, we discuss the brief history of TNBC classification and its implications for promising treatments.

Keywords

Acknowledgement

This research was supported by the Basic Science Research Capacity Enhancement Project through Korea Basic Science Institute (National Research Facilities and Equipment Center) grant funded by the Ministry of Education (Grant No. 2019R1A6C1010033).

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