The BAFF-APRIL System in Cancer

Author:

Ullah Md Ashik1ORCID,Mackay Fabienne1234

Affiliation:

1. Laboratory of B-Lymphocytes in Autoimmunity and Malignancies, QIMR Berghofer Medical Research Institute, Herston, QLD 4006, Australia

2. The Department of Microbiology and Immunology, Faculty of Medicine, Dentistry and Health Sciences, School of Biomedical Sciences, University of Melbourne, Parkville, VIC 3010, Australia

3. The Department of Immunology and Pathology, Monash University, Prahran, VIC 3004, Australia

4. Faculty of Medicine, University of Queensland, Brisbane, QLD 4006, Australia

Abstract

B cell-activating factor (BAFF; also known as CD257, TNFSF13B, BLyS) and a proliferation-inducing ligand (APRIL; also known as CD256, TNFSF13) belong to the tumor necrosis factor (TNF) family. BAFF was initially discovered as a B-cell survival factor, whereas APRIL was first identified as a protein highly expressed in various cancers. These discoveries were followed by over two decades of extensive research effort, which identified overlapping signaling cascades between BAFF and APRIL, controlling immune homeostasis in health and driving pathogenesis in autoimmunity and cancer, the latter being the focus of this review. High levels of BAFF, APRIL, and their receptors have been detected in different cancers and found to be associated with disease severity and treatment response. Here, we have summarized the role of the BAFF-APRIL system in immune cell differentiation and immune tolerance and detailed its pathogenic functions in hematological and solid cancers. We also highlight the emerging therapeutics targeting the BAFF-APRIL system in different cancer types.

Funder

National Health and Medical Research Council of Australia

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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