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Cancer immortality represents high plasticity and tolerance, and incomplete treatment methods such as microwave ablation (MWA) remodel the residual cancer microenvironment to further potentiate cancer resistance. Nanomedicine is a solution, but the serum protein corona and abnormal intratumoral blood vessels attenuate their delivery efficiency. Herein, protein corona-detachable MWA amplifiers consisting of O-binding mesoporous silica nanoparticles and doxorubicin (DOX) have been engineered. Such MWA amplifiers can achieve MWA-triggered O release to assist in detaching the adsorbed protein corona and reoxygenate MWA-aggravated hypoxic tumor to normalize intratumoral blood vessels, respectively, which favor amplifier delivery into tumor, addressing the above two delivery hurdles. Their multiple action mechanisms actuate the nonclassical pyroptosis pathway to activate premature cellular senescence, which dampens inherent and MWA-aggravated cancer stemness, plasticity, and DOX chemoresistance especially after uniting with MWA-aggravated hypoxic microenvironment reversion. Additionally, the above action rationales promote O bubble-mediated inertial cavitation to boost MWA outcome with repressed tumor residues after MWA. Collectively, such MWA amplifiers successfully target protein corona detachment, vascular normalization, cancer immorality repolarization into senescence, pyroptosis activation, and hypoxic microenvironment attenuation, thereby providing more enlightenment and insights into incomplete cancer therapy.
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http://dx.doi.org/10.1021/acsnano.5c08379 | DOI Listing |
ACS Nano
September 2025
State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
Nanoparticles bind to proteins in cells selectively and form a protein corona around them. However, the mechanisms of protein conformational changes underlying the interactions between nanoparticles and protein coronas remain poorly understood. In this study, we prepared small molecule self-assembled nanoparticles (Aloin NPs) as a research tool to investigate the allosteric mechanism of protein coronas.
View Article and Find Full Text PDFJ Appl Toxicol
September 2025
School of Engineering and Technology, National Forensic Science University, Gandhinagar, India.
Microplastics and nanoplastics (MNPs) are common pollutants that engage with proteins, lipids, nucleic acids, and other biomolecules, damaging cell structure. This review goes beyond simply listing where MNPs are found to explore how they cause harm, detailing mechanisms such as oxidative stress, endocrine disruption, genotoxicity, protein misfolding, lipid membrane destabilization, and epigenetic changes. Propose an integrated mechanistic hypothesis connecting these processes via oxidative epigenetic feedback loops, size-dependent organelle targeting, and pollutant corona effects, with potential implications for cellular aging and transgenerational outcomes.
View Article and Find Full Text PDFJ Comput Chem
September 2025
Johnson & Johnson, Beerse, Belgium.
Herein we report the in silico discovery of 13 novel micromolar potent inhibitors of the SARS-CoV-2 NSP13 helicase validated in cellular antiviral and biophysical ThermoFluor assays. The compounds, discovered using a novel fragment-based pharmacophore virtual screening workflow named FragmentScout, enable the advancement of novel antiviral agents. FragmentScout uses publicly accessible structural data of the SARS-CoV-2 NSP13 helicase, which was previously generated at the Diamond LightSource by XChem high-throughput crystallographic fragment screening.
View Article and Find Full Text PDFEur J Pain
October 2025
Headache Science and Neurorehabilitation Unit, IRCCS Mondino Foundation, Pavia, Italy.
Background: Although robust genetic markers for episodic migraine (EM) have been identified, variants associated with chronic migraine (CM) are still unknown. Given the potential pathophysiologic overlap between EM and CM, we investigated whether six single nucleotide polymorphisms (SNPs), robustly associated with EM susceptibility (LRP1 rs11172113, PRDM16 rs10797381, FHL5 rs7775721, TRPM8 rs10166942, near TSPAN2 rs2078371 and MEF2D rs1925950) also play a role in the risk of developing CM.
Methods: A total of 200 EM and 202 CM participants were prospectively included.
Adv Sci (Weinh)
September 2025
Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, 266003, P. R. China.
Protein corona alters the biological identities and interactions of nanoparticles with cells, needing to be thoroughly scrutinized before in vivo applications. Importantly, protein corona is evolving as nanoparticles cross different microenvironments, leading to unpredictable biological behaviors. Unveiling how physiological conditions change, especially pH changes associated with tumor-targeted delivery, affect protein corona composition and subsequent bio-interactions, is thus essential for understanding the bio-fate and therapeutic efficacy of nanomedicines.
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