Citrullination in tumor immunity and therapy

Peptidyl arginine deiminases (PADs) catalyze the conversion of arginine residues into peptidyl citrulline, a posttranslational modification known as protein citrullination (or arginine deimination). This process alters the charge of proteins from positive to neutral, thereby affecting their folding, stability, conformation, and function. PAD2 and PAD4 can translocate into the nucleus and citrullinate both cytoplasmic and nuclear proteins. In this Review, we focus on PAD2- and PAD4-mediated citrullination in immune cell subsets within the tumor microenvironment. We discuss how citrullination regulates immune cell function and tumor immunity and explore the potential of targeting citrullination as a strategy for cancer immunotherapy.

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Publication Details

Journal
Journal of Clinical Investigation
Published
2025-10-14
DOI
https://doi.org/10.1172/jci196348
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
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article

Citrullination in tumor immunity and therapy

Michael Pitter, Weiping Zou
Journal of Clinical Investigation
Glycosylation and Glycoproteins Research
article

Citrullination in tumor immunity and therapy

Michael Pitter, Weiping Zou
article en

Abstract

Peptidyl arginine deiminases (PADs) catalyze the conversion of arginine residues into peptidyl citrulline, a posttranslational modification known as protein citrullination (or arginine deimination). This process alters the charge of proteins from positive to neutral, thereby affecting their folding, stability, conformation, and function. PAD2 and PAD4 can translocate into the nucleus and citrullinate both cytoplasmic and nuclear proteins. In this Review, we focus on PAD2- and PAD4-mediated citrullination in immune cell subsets within the tumor microenvironment. We discuss how citrullination regulates immune cell function and tumor immunity and explore the potential of targeting citrullination as a strategy for cancer immunotherapy.

Journal of Clinical InvestigationVol. 135(20)
University of Michigan (US)
Openalex Percentile: Top 74%
Glycosylation and Glycoproteins Research
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