<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(1)</volume><submitter>Xiao Y</submitter><pubmed_abstract>Insufficient immune cell infiltration into the tumor microenvironment (TME) greatly compromises the clinical application of immune-checkpoint inhibitors (ICIs)-based immunotherapy. Recent findings have shown that activation of the cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS-STING) pathway can enhance natural immunity and increase lymphocyte infiltration into the TME, which presents a promising strategy for cancer immunotherapy. In this study, we constructed hydroxyapatite nanoparticles co-loaded with curcumin and L-oxaliplatin (Cur/L-OHP@HAP NPs). We analyzed the particle-size distribution, zeta potential, spectral characteristics (Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, ultraviolet-visible spectroscopy), and drug-release properties of th</pubmed_abstract><journal>Bioengineering &amp; translational medicine</journal><pagination>e10610</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10771561</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Curcumin/L-OHP co-loaded HAP for cGAS-STING pathway activation to enhance the natural immune response in colorectal cancer.</pubmed_title><pmcid>PMC10771561</pmcid><pubmed_authors>Jiang Z</pubmed_authors><pubmed_authors>Zhang F</pubmed_authors><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Peng B</pubmed_authors><pubmed_authors>Xiao Y</pubmed_authors><pubmed_authors>Guo G</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Liang M</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Li B</pubmed_authors><pubmed_authors>Qu G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Curcumin/L-OHP co-loaded HAP for cGAS-STING pathway activation to enhance the natural immune response in colorectal cancer.</name><description>Insufficient immune cell infiltration into the tumor microenvironment (TME) greatly compromises the clinical application of immune-checkpoint inhibitors (ICIs)-based immunotherapy. Recent findings have shown that activation of the cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS-STING) pathway can enhance natural immunity and increase lymphocyte infiltration into the TME, which presents a promising strategy for cancer immunotherapy. In this study, we constructed hydroxyapatite nanoparticles co-loaded with curcumin and L-oxaliplatin (Cur/L-OHP@HAP NPs). We analyzed the particle-size distribution, zeta potential, spectral characteristics (Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, ultraviolet-visible spectroscopy), and drug-release properties of th</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2025-04-05T10:45:17.544Z</modification><creation>2025-02-19T03:18:06.719Z</creation></dates><accession>S-EPMC10771561</accession><cross_references><pubmed>38193125</pubmed><doi>10.1002/btm2.10610</doi></cross_references></HashMap>