Type 2 Cystatins and Their Roles in the Regulation of Human Immune Response and Cancer Progression

Author:

Zhang Zijun1,Zhan Fenghuang1

Affiliation:

1. Myeloma Center, Winthrop P. Rockefeller Cancer Institute, Department of Internal Medicine, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA

Abstract

Cystatins are a family of intracellular and extracellular protease inhibitors that inhibit cysteine cathepsins—a group of lysosomal cysteine proteases that participate in multiple biological processes, including protein degradation and post-translational cleavage. Cysteine cathepsins are associated with the development of autoimmune diseases, tumor progression, and metastasis. Cystatins are categorized into three subfamilies: type 1, type 2, and type 3. The type 2 cystatin subfamily is the largest, containing 10 members, and consists entirely of small secreted proteins. Although type 2 cystatins have many shared biological roles, each member differs in structure, post-translational modifications (e.g., glycosylation), and expression in different cell types. These distinctions allow the type 2 cystatins to have unique biological functions and properties. This review provides an overview of type 2 cystatins, including their biological similarities and differences, their regulatory effect on human immune responses, and their roles in tumor progression, immune evasion, and metastasis.

Funder

National Cancer Institute

U.S. Department of Defense

Myeloma Crowd Research Initiative Award

Paula and Rodger Riney Foundation

UAMS Winthrop P. Rockefeller Cancer Institute (WRCRI) Fund

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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