ReviewInternational journal of nanomedicine2025
Nanomaterial-Driven Regulated Cell Death: Mechanistic Insights and Novel Strategies for Tumor Therapy.
Review in International journal of nanomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Anticancer Activity of Green Synthesized ZnO Nanoparticles fromNanomaterials (Basel, Switzerland) · 2026Article
- Regulated cell death in ovarian cancer: molecular mechanisms and therapeutic targets.Frontiers in cell and developmental biology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The rapid development of nanomaterials (NMs) and nanotechnology has profoundly impacted the biomedical field. Due to their unique physicochemical properties, NMs can interact with biological molecules, including proteins and DNA, to induce regulated cell death (RCD). Recent studies have demonstrated that NMs trigger RCD by promoting reactive oxygen species generation, activating signaling proteins, and disrupting intracellular ion homeostasis. Among the various forms of RCD, necroptosis, pyroptosis, ferroptosis, and cuproptosis have garnered significant research attention. Increasing evidence suggests that these emerging RCD pathways are crucial for tumor proliferation and migration, tumor microenvironment (TME) remodeling, and drug resistance mitigation. Accordingly, leveraging NM-driven RCD's effects in designing multifunctional drug delivery systems holds great promise for cancer therapy. NMs can also serve as versatile drug carriers in synergistic treatments with targeting agents, photothermal/photodynamic therapy, and immunomodulators, thereby overcoming the limitations of conventional treatments. Collectively, this review systematically summarizes recent advancements in NM-induced RCD in cancer cells and discusses the diverse roles of RCD in tumor pathology. We highlight the innovative potential of NMs in inducing RCD through precise targeting and synergistic therapy, offering novel strategies to overcome tumor resistance and reshape the immunosuppressive TME.
Indexed as
Identifiers
What Socratic holds
Registered trials
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 Socratic graph.