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The Hyaluronan/CD44 Axis: A Double-Edged Sword in Cancer

Hyaluronic acid (HA) receptor CD44 is widely used for identifying cancer stem cells and its activation promotes stemness. Recent evidence shows that overexpression of CD44 is associated with poor prognosis in most human cancers and mediates therapy resistance. For these reasons, in recent years, CD4...

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Detalles Bibliográficos
Autor principal: Cirillo, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10649834/
https://www.ncbi.nlm.nih.gov/pubmed/37958796
http://dx.doi.org/10.3390/ijms242115812
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author Cirillo, Nicola
author_facet Cirillo, Nicola
author_sort Cirillo, Nicola
collection PubMed
description Hyaluronic acid (HA) receptor CD44 is widely used for identifying cancer stem cells and its activation promotes stemness. Recent evidence shows that overexpression of CD44 is associated with poor prognosis in most human cancers and mediates therapy resistance. For these reasons, in recent years, CD44 has become a treatment target in precision oncology, often via HA-conjugated antineoplastic drugs. Importantly, HA molecules of different sizes have a dual effect and, therefore, may enhance or attenuate the CD44-mediated signaling pathways, as they compete with endogenous HA for binding to the receptors. The magnitude of these effects could be crucial for cancer progression, as well as for driving the inflammatory response in the tumor microenvironment. The increasingly common use of HA-conjugated drugs in oncology, as well as HA-based compounds as adjuvants in cancer treatment, adds further complexity to the understanding of the net effect of hyaluronan-CD44 activation in cancers. In this review, I focus on the significance of CD44 in malignancy and discuss the dichotomous function of the hyaluronan/CD44 axis in cancer progression.
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spelling pubmed-106498342023-10-31 The Hyaluronan/CD44 Axis: A Double-Edged Sword in Cancer Cirillo, Nicola Int J Mol Sci Review Hyaluronic acid (HA) receptor CD44 is widely used for identifying cancer stem cells and its activation promotes stemness. Recent evidence shows that overexpression of CD44 is associated with poor prognosis in most human cancers and mediates therapy resistance. For these reasons, in recent years, CD44 has become a treatment target in precision oncology, often via HA-conjugated antineoplastic drugs. Importantly, HA molecules of different sizes have a dual effect and, therefore, may enhance or attenuate the CD44-mediated signaling pathways, as they compete with endogenous HA for binding to the receptors. The magnitude of these effects could be crucial for cancer progression, as well as for driving the inflammatory response in the tumor microenvironment. The increasingly common use of HA-conjugated drugs in oncology, as well as HA-based compounds as adjuvants in cancer treatment, adds further complexity to the understanding of the net effect of hyaluronan-CD44 activation in cancers. In this review, I focus on the significance of CD44 in malignancy and discuss the dichotomous function of the hyaluronan/CD44 axis in cancer progression. MDPI 2023-10-31 /pmc/articles/PMC10649834/ /pubmed/37958796 http://dx.doi.org/10.3390/ijms242115812 Text en © 2023 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Cirillo, Nicola
The Hyaluronan/CD44 Axis: A Double-Edged Sword in Cancer
title The Hyaluronan/CD44 Axis: A Double-Edged Sword in Cancer
title_full The Hyaluronan/CD44 Axis: A Double-Edged Sword in Cancer
title_fullStr The Hyaluronan/CD44 Axis: A Double-Edged Sword in Cancer
title_full_unstemmed The Hyaluronan/CD44 Axis: A Double-Edged Sword in Cancer
title_short The Hyaluronan/CD44 Axis: A Double-Edged Sword in Cancer
title_sort hyaluronan/cd44 axis: a double-edged sword in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10649834/
https://www.ncbi.nlm.nih.gov/pubmed/37958796
http://dx.doi.org/10.3390/ijms242115812
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