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A tumor-associated heparan sulfate-related glycosaminoglycan promotes the generation of functional regulatory T cells

Authors :
Leticia Martín-Cruz
Marcos Viñuela
Ioanna Kalograiaki
Alba Angelina
Paola Oquist-Phillips
Irene Real-Arévalo
Francisco Javier Cañada
José Ignacio Tudela
Luis Moltó
Jesús Moreno-Sierra
José Luis Subiza
Oscar Palomares
Moreno Sierra, Jesús
Martín De La Cruz, Leticia
Angelina Querencias, Alba
Palomares Gracia, Óscar
Leticia Martín-Cruz
Marcos Viñuela
Ioanna Kalograiaki
Alba Angelina
Paola Oquist-Phillips
Irene Real-Arévalo
Francisco Javier Cañada
José Ignacio Tudela
Luis Moltó
Jesús Moreno-Sierra
José Luis Subiza
Oscar Palomares
Moreno Sierra, Jesús
Martín De La Cruz, Leticia
Angelina Querencias, Alba
Palomares Gracia, Óscar
Publication Year :
2024

Abstract

Functional Tregs play a key role in tumor development and progression, representing a major barrier to anticancer immunity. The mechanisms by which Tregs are generated in cancer and the influence of the tumor microenvironment on these processes remain incompletely understood. Herein, by using NMR, chemoenzymatic structural assays and a plethora of in vitro and in vivo functional analyses, we demonstrate that the tumoral carbohydrate A10 (Ca10), a cell-surface carbohydrate derived from Ehrlich’s tumor (ET) cells, is a heparan sulfate-related proteoglycan that enhances glycolysis and promotes the development of tolerogenic features in human DCs. Ca10-stimulated human DCs generate highly suppressive Tregs by mechanisms partially dependent on metabolic reprogramming, PD-L1, IL-10, and IDO. Ca10 also reprograms the differentiation of human monocytes into DCs with tolerogenic features. In solid ET-bearing mice, we found positive correlations between Ca10 serum levels, tumor size and splenic Treg numbers. Administration of isolated Ca10 also increases the proportion of splenic Tregs in tumor-free mice. Remarkably, we provide evidence supporting the presence of a circulating human Ca10 counterpart (Ca10H) and show, for the first time, that serum levels of Ca10H are increased in patients suffering from different cancer types compared to healthy individuals. Of note, these levels are higher in prostate cancer patients with bone metastases than in prostate cancer patients without metastases. Collectively, we reveal novel molecular mechanisms by which heparan sulfate-related structures associated with tumor cells promote the generation of functional Tregs in cancer. The discovery of this novel structural-functional relationship may open new avenues of research with important clinical implications in cancer treatment.<br />MINECO<br />Ministerio de Ciencia e Innovación<br />Depto. de Bioquímica y Biología Molecular<br />Fac. de Ciencias Químicas<br />TRUE<br />pub

Details

Database :
OAIster
Notes :
application/pdf, 2042-0226, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1429623303
Document Type :
Electronic Resource