Leukocyte immunoglobulin-like receptor subfamily B: therapeutic targets in cancer

Author:

Deng Mi1ORCID,Chen Heyu1,Liu Xiaoye1,Huang Ryan1,He Yubo1,Yoo Byounggyu1,Xie Jingjing1,John Samuel2,Zhang Ningyan3,An Zhiqiang3ORCID,Zhang Cheng Cheng1

Affiliation:

1. Department of Physiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

2. Department of Pediatrics, Pediatric Hematology-Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

3. Texas Therapeutics Institute, Brown Foundation Institute of Molecular Medicine, University of Texas Houston Health Science Center, Houston, TX 77030, USA

Abstract

Abstract Inhibitory leukocyte immunoglobulin-like receptors (LILRBs 1–5) transduce signals via intracellular immunoreceptor tyrosine-based inhibitory motifs that recruit phosphatases to negatively regulate immune activation. The activation of LILRB signaling in immune cells may contribute to immune evasion. In addition, the expression and signaling of LILRBs in cancer cells especially in certain hematologic malignant cells directly support cancer development. Certain LILRBs thus have dual roles in cancer biology—as immune checkpoint molecules and tumor-supporting factors. Here, we review the expression, ligands, signaling, and functions of LILRBs, as well as therapeutic development targeting them. LILRBs may represent attractive targets for cancer treatment, and antagonizing LILRB signaling may prove to be effective anti-cancer strategies.

Funder

National Cancer Institute

Cancer Prevention and Research Institute of Texas

Immune-Onc Therapeutics

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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