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Article: Hyperbaric Oxygen Regulates Tumor pH to Boost Copper-Doped Hydroxyethyl Starch Conjugate Nanoparticles Against Cancer Stem Cells

TitleHyperbaric Oxygen Regulates Tumor pH to Boost Copper-Doped Hydroxyethyl Starch Conjugate Nanoparticles Against Cancer Stem Cells
Authors
Keywordscancer stem cells
carbonic anhydrase 9
hyperbaric oxygen
nanomedicine
tumor pH
Issue Date1-Aug-2025
PublisherJohn Wiley & Sons
Citation
Exploration, 2025, v. 5, n. 4 How to Cite?
Abstract

An extracellular acidic environment and an intracellular mildly alkaline environment induced by carbonic anhydrase 9 (CA9) play a critical role in self-renewal, invasion, migration, and drug resistance of cancer stem cells (CSCs) within hypoxic solid tumors. Here, we report an antitumor strategy leveraging hyperbaric oxygen therapy (HBO) to regulate tumor pH and boost hydroxyethyl starch-doxorubicin-copper nanoparticles (HHD-Cu NPs) against CSCs. HBO overcomes tumor hypoxia, downregulates pH-regulatory proteins such as CA9, and leads to intracellular accumulation of acidic metabolites. As a result, HBO promotes intracellular acidification of both tumor cells and CSCs, triggering efficient doxorubicin release and the potent copper-mediated chemical dynamic effect of subsequently administered dual-acid-responsive HHD-Cu NPs. The combination of HBO with HHD-Cu NPs not only eliminates tumor cells but also inhibits CSCs, altogether leading to potent tumor inhibition. This study explores a new function of clinical-widely used HBO and establishes a novel combination therapy for treating CSCs abundant hypoxic solid tumors.


Persistent Identifierhttp://hdl.handle.net/10722/360811
ISSN

 

DC FieldValueLanguage
dc.contributor.authorDeng, Qingyuan-
dc.contributor.authorHua, Ao-
dc.contributor.authorLi, Shiyou-
dc.contributor.authorZhang, Zhijie-
dc.contributor.authorChen, Xiang-
dc.contributor.authorWang, Qiang-
dc.contributor.authorWang, Xing-
dc.contributor.authorChu, Zhiqin-
dc.contributor.authorYang, Xiangliang-
dc.contributor.authorLi, Zifu-
dc.date.accessioned2025-09-16T00:30:39Z-
dc.date.available2025-09-16T00:30:39Z-
dc.date.issued2025-08-01-
dc.identifier.citationExploration, 2025, v. 5, n. 4-
dc.identifier.issn2766-8509-
dc.identifier.urihttp://hdl.handle.net/10722/360811-
dc.description.abstract<p>An extracellular acidic environment and an intracellular mildly alkaline environment induced by carbonic anhydrase 9 (CA9) play a critical role in self-renewal, invasion, migration, and drug resistance of cancer stem cells (CSCs) within hypoxic solid tumors. Here, we report an antitumor strategy leveraging hyperbaric oxygen therapy (HBO) to regulate tumor pH and boost hydroxyethyl starch-doxorubicin-copper nanoparticles (HHD-Cu NPs) against CSCs. HBO overcomes tumor hypoxia, downregulates pH-regulatory proteins such as CA9, and leads to intracellular accumulation of acidic metabolites. As a result, HBO promotes intracellular acidification of both tumor cells and CSCs, triggering efficient doxorubicin release and the potent copper-mediated chemical dynamic effect of subsequently administered dual-acid-responsive HHD-Cu NPs. The combination of HBO with HHD-Cu NPs not only eliminates tumor cells but also inhibits CSCs, altogether leading to potent tumor inhibition. This study explores a new function of clinical-widely used HBO and establishes a novel combination therapy for treating CSCs abundant hypoxic solid tumors.</p>-
dc.languageeng-
dc.publisherJohn Wiley & Sons-
dc.relation.ispartofExploration-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectcancer stem cells-
dc.subjectcarbonic anhydrase 9-
dc.subjecthyperbaric oxygen-
dc.subjectnanomedicine-
dc.subjecttumor pH-
dc.titleHyperbaric Oxygen Regulates Tumor pH to Boost Copper-Doped Hydroxyethyl Starch Conjugate Nanoparticles Against Cancer Stem Cells-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1002/EXP.20240080-
dc.identifier.scopuseid_2-s2.0-105002120513-
dc.identifier.volume5-
dc.identifier.issue4-
dc.identifier.eissn2766-2098-
dc.identifier.issnl2766-2098-

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