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. 2020 Mar 29;12(4):819. doi: 10.3390/cancers12040819

Table 1.

Classifications of triple negative breast cancer (TNBC).

Subtypes Characteristics
LEHMANN CLASSIFICATION [6]
Basal-like 1 High level of DNA repair proteins and cell-cycle regulation (high rate of tp53 mutations, amplification of MYC, CDK6, CCNE1, deletion of BRCA-2, PTEN, MDM2, RB1).
Basal-like 2 Overexpression of growth factor signaling genes and overexpression of myoepithelial differentiation genes.
Mesenchymal like Expression of genes associated with EMT.
Mesenchymal-stem like Expression of genes associated with EMT;
Enrichment in genes involved in angiogenesis, including VEGFR2 and some components of immune signaling;
High expression of stem cells genes;
Low expression of proliferation genes and epithelial-related genes involved in the maintenance of cellular junction, such as claudin (claudin-low breast cancer).
Immunomodulatory Enrichment in genes involved in regulation of immune response, antigen processing and presentation, immune cells and cytokine signaling pathways.
Luminal androgen receptor (LAR) High level of androgen receptor genes;
Alterations of PI3K pathway genes (PI3KCA, AKT1, NF1, CDH1).
BURSTEIN CLASSIFICATION [7]
Basal-like immunosuppressed (BLIS) Downregulation of B cell, T cell, and natural killer cell immune-regulating pathways, and cytokine pathways;
Expression of multiple SOX family transcription factors.
Basal-like immunoactivated (BLIA) Upregulation of genes involved in immune cell function regulation;
High expression of STAT genes.
Mesenchymal (MES) Expression of genes involved in cell cycle, mismatch repair, and DNA damage networks, and hereditary breast cancer signaling pathways;
Expression of genes normally exclusive to osteocytes (OGN) and adipocytes (ADIPOQ, PLIN1) and important growth factors (IGF1).
Luminal androgen receptor (LAR) Expression of AR, ER, prolactin, and ErbB4 signaling genes.
MICROARRAY-BASED CLASSIFICATION [4,5]
Basal-like Low expression of luminal A signature, high proliferation score, low expression of estrogen signaling related genes (FOXA1, PGR); High expression of cell-cycle related genes (CCNE, FANCA); High expression of EMT (TWIST1, ZEB1).
Claudin-low Low levels of cell adhesion proteins (Claudins 3, 4, 7, Occludin, E-caderin); Low expression of luminal genes; Inconsistent basal genes expression; Elevated expression of immune-related genes (CD4, CD79a).
Molecular apocrine Activation of AR pathways.
Interferon-rich Overexpression of interferon-regulated genes (STAT1, SP110).

Epithelial-mesenchymal transition, EMT; androgen receptor, AR; estrogen receptor, ER.