Evidence map›Paper›PMID 41965546›Full record

ArticleBMC cancer2026

RGD-modified hollow mesoporous nanoparticles loaded with cisplatin for antitumor therapy in colon cancer.

Xiaohou Xi, Bohao Zhang

Abstract read
In one paragraph

Article in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Xiaohou XiDepartment of Gastroenterology, Jilin Province People´s Hospital, Changchun, Jilin, 130021, People's Republic of China.
Bohao ZhangDepartment of Oncology, Xi'an International Medical Center Hospital, Xi'an, Shaanxi, 710100, People's Republic of China. raida1222@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo develop an Arg-Gly-Asp peptide (RGD)-targeted hollow mesoporous manganese dioxide nanoparticle system loaded with cisplatin (RGD-HMnO₂/CDDP) and evaluate its in vitro antitumor activity, in vivo therapeutic efficacy, and mechanisms in colon cancer.

methodsHollow MnO₂ (HMnO₂) was fabricated using SiO₂ nanospheres as a hard template via KMnO₄ oxidative deposition followed by Na₂CO₃ etching. Cisplatin was loaded and RGD peptides were conjugated to obtain RGD-HMnO₂/CDDP. Morphology and physicochemical properties were characterized by TEM, XRD, XPS, DLS, and zeta potential. In CT26 cells, cytotoxicity (CCK-8), invasion/migration (Transwell), reactive oxygen species (ROS, DCFH-DA), mitochondrial membrane potential (JC-1), DNA damage (γ-H2AX), apoptosis (Western blot; Annexin V-FITC/PI) were assessed. In tumor-bearing mice, antitumor efficacy, serum cytokines (TNF-α, IFN-γ, IL-6, IL-2, IL-10), and hematological indices were evaluated.

resultsRGD-HMnO₂/CDDP showed markedly enhanced cytotoxicity versus free cisplatin and non-targeted HMnO₂/CDDP, and significantly inhibited invasion and migration. Mechanistically, it increased intracellular ROS, induced mitochondrial depolarization, elevated γ-H2AX, and activated apoptosis signaling, resulting in higher apoptotic rates. In vivo, RGD-HMnO₂/CDDP achieved superior tumor growth inhibition, modulated inflammatory/immune cytokines, and maintained favorable hematological profiles, indicating good immunomodulation and biocompatibility.

conclusionRGD-HMnO₂/CDDP enhances cisplatin efficacy against colon cancer by promoting ROS-driven mitochondrial dysfunction and DNA damage–associated apoptosis, with potential improvement of the tumor immune microenvironment and without compromising systemic safety.

Indexed as

Antineoplastic AgentsCisplatinColonic NeoplasmsNanoparticlesOligopeptidesAnimalsApoptosisCell Line, TumorCytokinesDrug CarriersHumansManganese CompoundsMembrane Potential, MitochondrialMiceOxidesPorosityAntineoplastic Agentsarginyl-glycyl-aspartic acidCisplatinCytokinesDrug CarriersManganese Compoundsmanganese dioxideOligopeptidesOxidesReactive Oxygen SpeciesCisplatinColon cancerHollow mesoporous manganese dioxideNanodrug delivery systemRGD peptideTumor immune microenvironment

Identifiers

PMID41965546
PMCPMC13188791

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.