Target intelligence / Profile preview

TCR gamma alternate reading frame protein (TARP) (TARP)

Target
TARP
Molecular classification
Tumor-associated antigen, Intracellular protein
01

Overview

TCR gamma alternate reading frame protein (TARP) is a 58-amino acid tumor-associated antigen encoded by an alternative reading frame of the T-cell receptor gamma (TRG) locus [1, 2]. It is predominantly expressed in the mitochondria of over 95% of prostate cancers and approximately 50% of breast cancers, while its expression in normal tissues is largely restricted to the prostate and salivary glands [2, 3]. As a tumor-associated antigen, TARP is processed into immunogenic peptides, most notably the TARP(27-35) epitope, which is presented on the cell surface by the HLA-A*0201 major histocompatibility complex [3, 4]. This specific presentation makes TARP an ideal target for immunotherapeutic interventions, including peptide-based vaccines and T-cell receptor (TCR) engineered T-cell therapies [4, 5]. Clinical trials have demonstrated that TARP-targeted vaccines can induce robust cytotoxic T-lymphocyte responses, which are associated with a decrease in PSA velocity in patients with biochemical recurrence of prostate cancer [3, 6].

Other names
T-cell receptor gamma alternate reading frame proteinTARP antigenTRG alternate reading frame protein
02

Mechanism of action

Activation of the immune system to recognize and destroy tumor cells by targeting specific TARP-derived peptides presented on the HLA-A*0201 major histocompatibility complex.

03

Biological functions

Immune responseCell proliferationMitochondrial regulation
04

Disease associations

Prostate cancerBreast cancer
05

Safety considerations

On-target off-tumor toxicity to normal prostate or salivary gland tissueImmune escape via HLA downregulation or antigen lossPotential for autoimmune reactions
06

Interacting drugs

TARP peptide vaccine

3 more in the full profile.

07

Biomarkers

HLA-A*0201 genotypeTARP mRNA expressionProstate-specific antigen (PSA) doubling time

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