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Breast cancer tumor antigens

Molecular classification
Receptor, Growth factor receptor, Transmembrane protein, Glycoprotein
01

Overview

Breast cancer tumor antigens are proteins expressed on breast cancer cells that can be targeted by the immune system or therapeutic interventions. The most well-characterized breast cancer antigen is Human Epidermal Growth Factor Receptor 2 (HER2), which is overexpressed in approximately 15-20% of breast cancers[5][6]. HER2 is a 185-kDa protein receptor with tyrosine kinase activity that plays a crucial role in cell proliferation and survival[1]. Other important breast cancer antigens include Carcinoembryonic Antigen (CEA), Mucin 1 (MUC-1), carbohydrate antigens (Tn, TF, STn), p53, telomerase reverse transcriptase (TERT), and Wilms' tumor 1 (WT1)[1]. These antigens can be classified as tumor-associated antigens (TAAs), which are self-proteins abnormally expressed in cancer cells, or tumor-specific antigens (TSAs), which are unique to cancer cells[3]. Neoantigens, a type of TSA arising from somatic mutations, are particularly important in breast cancer immunotherapy. Triple-negative breast cancers (TNBC) typically have a higher neoantigen burden compared to hormone receptor-positive (HR+) breast cancers, which correlates with increased immune infiltration and better response to immunotherapy[4]. Targeted therapies against breast cancer antigens include monoclonal antibodies like trastuzumab, which binds to the extracellular domain of HER2 and blocks its activation[5][6]. These targeted approaches have significantly improved outcomes for patients with HER2-positive breast cancer. The molecular classification of breast cancer based on antigen expression (HER2, ER, PR, Ki-67) helps guide treatment decisions and predict prognosis[6].

Other names
Tumor-associated antigens (TAAs)Tumor-specific antigens (TSAs)Breast cancer neoantigens
02

Mechanism of action

Antibody-dependent cell-mediated cytotoxicity; Blocking of signaling pathways; Inhibition of cell proliferation; Enhancement of immune recognition; Induction of cancer cell death

03

Biological functions

Cell proliferationCell signalingCell survivalMetastasisImmune evasion
04

Disease associations

CancerBreast cancer progressionMetastatic breast cancer
05

Safety considerations

Autoimmune reactionsLimited specificity for some antigensResistance developmentVariable expression across patients
06

Interacting drugs

6 more in the full profile.

07

Biomarkers

HER2 overexpressionEstrogen receptor (ER) statusProgesterone receptor (PR) statusKi-67 expressionTumor mutational burden (TMB)

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