Skip to main content

Table 1 Transcriptomic and proteomic classifiers of triple negative breast cancer

From: Heterogeneity of triple negative breast cancer: Current advances in subtyping and treatment implications

TNBC

Classifier

Year

Number of TNBC cases

Subtypes

Biological level information

Key clinical findings

Transcriptomic profiling

Lehmann et al.[4]

Lehmann et al. [57]

2011

Refined in

2016

587

6 main subtypes:

Basal-like 1

Basal-like 2 Immunomodulatory

Luminal androgen receptor

Mesenchymal

Mesenchymal stem-like

RNA expression

Basal-like 1 had a higher pathologic complete response rate after neoadjuvant chemotherapy and a better overall survival

   

4 main subtypes:

Basal-like 1

Basal-like 2

Luminal androgen receptor

Mesenchymal

  

Burstein et al. [7]

2015

198

4 main subtypes:

Basal-like immune activated

Basal-like immune suppressed

Luminal androgen receptor

Mesenchymal

RNA expression and DNA copy number

Four clinically distinct subtypes

Survival outcomes were most favorable for basal-like immune activated

and worst for basal-like immune suppressed

Jiang et al.[6]

2019

504

4 main subtypes:

Immunomodulatory

Basal-like immune suppressed

Luminal androgen receptor

Mesenchymal

RNA expression, DNA copy number and somatic mutations

Distinct patterns related to the Chinese TNBC population: higher frequencies of PIK3CA mutations and luminal androgen receptor subtype

Basal-like immune suppressed with high-homologous recombination deficiency scores had a better prognosis when compared to those with low scores

Bareche et al. [35]

2018

550

5 main subtypes:

Basal-like 1

Immunomodulatory

Luminal androgen receptor

Mesenchymal

Mesenchymal stem-like

RNA expression, DNA copy number and somatic mutations

Immunomodulatory subtype was significantly associated with a better prognosis

Luminal androgen receptor

and mesenchymal stem-like subtypes were associated with low grade tumors

Proteomic profiling

Gong et al. [76]

2022

90 fresh- frozen

4 main subtypes

Immunomodulatory

Basal-like immune suppressed

Luminal androgen receptor

Mesenchymal

Global proteomics and phospho-proteomics

RNA expression, DNA copy number and somatic mutations

Four clinically distinct subtypes

The proteome subtype that resembled immunomodulatory had the best survival

while the proteome subtype that resembled luminal androgen receptor had the worst survival

Potential therapeutic targets involved in fatty acid metabolism (e.g. FASN) specifically for the proteome subtype that resembled luminal androgen receptor

A potential therapeutic target of NAE1 for the proteome subtype that resembled basal-like immune suppressed

Asleh et al. [60]

2022

88 Formalin- fixed paraffin-

embedded

4 main subtypes:

Basal-like immune activated

Basal-like immune suppressed

Luminal androgen receptor

Mesenchymal

Global proteomics

Four clinically distinct subtypes

Survival outcomes were most favorable for the proteome subtype that resembled basal-like immune activated

and worst for basal-like immune suppressed

Potential therapeutic targets involved in antigen presentation (e.g., TAP1, HLA-DQA1) for the proteome subtype that resembled basal-like immune activated

Potential therapeutic targets involved in fatty acid metabolism (e.g., FASN) for the proteome subtype that resembled luminal androgen receptor

  1. Abbreviations: TNBC triple negative breast cancer