4.6 Review

GARP: A Key Target to Evaluate Tumor Immunosuppressive Microenvironment

Journal

BIOLOGY-BASEL
Volume 10, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/biology10090836

Keywords

GARP; TGF-beta; cancer; biomarker; immunosuppression

Categories

Funding

  1. French Government by the French National Research Agency under the program Investissements d'Avenir [ANR- 11-LABX-0021, ANR-10-EQPX-05-01/IMAPPI Equipex, ANR-15-IDEX-0003]
  2. Centre George-Francois Leclerc

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GARP is widely expressed in cancer and plays a crucial role in the TGF-beta pathway, promoting cancer progression and contributing to immune evasion. Its potential as a predictive and therapeutic biomarker in real time assessment through molecular imaging is also highlighted.
Glycoprotein-A repetitions predominant (GARP) is the docking receptor for latent transforming growth factor (LTGF-beta) and promotes its activation. In cancer, increased GARP expression has been found in many types of cancer. GARP is expressed by regulatory T cells and platelets in the tumor microenvironment (TME) and can be also expressed by tumor cells themselves. Thus, GARP can be widely present in tumors in which it plays a major role in the production of active TGF-beta, contributing to immune evasion and cancer progression via the GARP-TGF-beta pathway. The objective of this review is to highlight GARP expression and function in cancer and to evaluate the potential of membrane GARP as a predictive and therapeutic follow-up biomarker that could be assessed, in real time, by molecular imaging. Moreover, as GARP can be secreted, a focus will also be made on soluble GARP as a circulating biomarker.

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