Skip to content
Review

Silver nanoparticles in tumor microenvironment modulation: Mechanistic insights, preclinical evidence, and translational challenges.

Aug 2026 · Seminars in Oncology · Vol 53 5, pp. 152537 · 0 citations · 175 references
Medicine

TL;DR

This review elucidates not only the features and components of the TME, but also explains the synthesis and mechanisms of action of AgNPs and puts in context their various applications in nanomedicine and cancer treatment.

Abstract

One of the world's major health challenges is cancer, which arises from sequential genetic and epigenetic alterations leading to tumor development and progression. The tumor microenvironment (TME), which consists of heterogeneous stroma and immune cells, is central to cancer progression, angiogenesis, immune evasion, and metastasis. TME modulation has become a potential strategy for cancer prevention and therapy. Nanoparticles of silver (AgNPs) possess distinct physicochemical characteristics that make them attractive candidates for therapeutic use via their capacity to generate oxidative stress, impair intracellular mechanisms, and impact immune signaling. This review elucidates not only the features and components of the TME, but also explains the synthesis and mechanisms of action of AgNPs, and puts in context their various applications in nanomedicine and cancer treatment. Although AgNPs show promising anticancer activity, toxicity, environmental risk, and clinical translation are still dominant areas for future research.

View source

Similar papers

Review Aug 2026

Mechanistic and Translational Insights into Gold Nanoparticle-based Cancer Immunotherapy: A Quantitative Comparative Review of Opportunities and Toxicological Challenges

Advances in nanotechnology have produced a range of strategies for cancer treatment. Among the materials under investigation, Gold Nanoparticles (AuNPs) are attractive candidates for immunotherapy because of their distinctive physicochemical properties and biocompatibility. This narrative review draws on stu...

V. R. Jallepalli, Angum M. M. Ibrahim, Anasuya Patil et al. · 0 citations
Review Open access Jul 2026

Zinc oxide nanoparticles as a plausible alternative to overcome contemporary chemotherapeutic challenges

The dysregulated mechanisms involved in carcinogenesis, the anti-proliferative activity of ZnO NPs, and their proficiency in target drug delivery to tumour cells are explored, using Google Scholar®, SciFinder® and PubMed® as search engines.

Badmus Jelili Abiodun, O. Afolabi · 0 citations
Review Open access Jul 2026

Metal-based nanodrugs for cancer immunotherapy: smart nanosystems, immunomodulatory mechanisms, and translational perspectives

This paper integrates metallobiology, nanomedicine, and tumor immunology to provide a theoretical framework for the precise design of smart metal immunotherapeutics, while identifying key challenges for clinical translation, such as the therapeutic safety window and metal homeostasis compensation mechanisms.

Shuyong Yan, Fei Zhou · 0 citations
Review Jul 2026

Mechanistic advances in nanomedicine, nucleic acid therapies, and AI-driven research on cervical cancer.

A translational framework for overcoming key barriers in pharmaceutical intervention design for oncology applications is outlined, integrating drug delivery engineering, molecular biopharmaceutics, and computational optimization.

Manoj Dalabehera, Shubham K. Chaudhari, Jatin Kumar et al. · 0 citations
Review Open access Aug 2026

Selenium nanoparticles for breast cancer: mechanisms, delivery strategies, and translational challenges

It is highlighted that future progress will depend on standardized formulations, rigorous in vivo validation, and biomarker-informed clinical development rather than unselected selenium use, with particular emphasis on selenium nanoparticles (SeNPs) as engineerable platforms for breast cancer therapy.

Hui-Jia Ni, Xu Fu, Xiaoyu Chen et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.