Evidence map›Paper›PMID 41098351›Full record

ReviewOncoTargets and therapy2025

Precision Nanomedicine for Cancer: Innovations, Strategies, and Translational Challenges.

Fuxing Wen, Lishuang Wang, Xian Li, Jiajia Zhao, Tingting Xu, Jingkai Zhu, Lijuan Ma, Xiaodong Wang

Abstract readReview
In one paragraph

Review in OncoTargets and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Bridging bioactive metabolites ofFrontiers in pharmacology · 2026
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
4 · The record

Corrections and comments

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

8 authors.

Fuxing WenJilin City Hospital of Chemical Industry, Department of Gastroenterology, Jilin City, Jilin, 132022, People's Republic of China.
Lishuang WangJilin City Hospital of Chemical Industry, Department of Cardiology, Jilin City, Jilin, 132022, People's Republic of China.
Xian LiJilin City Hospital of Chemical Industry, Hematology Department, Jilin City, Jilin, 132022, People's Republic of China.
Jiajia ZhaoThe Second Affiliated Hospital of Shaoyang University, Department of Gastroenterology, Shaoyang, Hunan, 422000, People's Republic of China.
Tingting XuJilin City Hospital of Chemical Industry, Department of Gastroenterology, Jilin City, Jilin, 132022, People's Republic of China.
Jingkai ZhuJilin City Hospital of Chemical Industry, Department of Gastroenterology, Jilin City, Jilin, 132022, People's Republic of China.
Lijuan MaJilin City Hospital of Chemical Industry, Department of Gastroenterology, Jilin City, Jilin, 132022, People's Republic of China.
Xiaodong WangThe Second Hospital of Jilin University, Gastroenteric Medicine and Digestive Endoscopy Center, Changchun, Jilin, 130041, People's Republic of China.ORCID 0000-0001-5924-4649

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As nanotechnology advances rapidly, it has propelled nanomedicine into a revolutionary frontier for anticancer therapy. This review comprehensively analyzes the core principles, key innovations, and strategic approaches driving the development of targeted nanotherapeutics against tumors. We elucidate the distinctive properties of nanoscale drug delivery systems (eg, liposomes, polymeric nanoparticles, inorganic nanoparticles, and hybrid systems) and their capacity to be designed to surmount the constraints of traditional cancer treatments by potentially augmenting drug specificity, bioavailability, and minimizing systemic toxicity, with some nanocarriers (eg, liposomal doxorubicin) already approved for clinical use. With a focus on both the enhanced permeability and retention (EPR) effect-mediated passive targeting and ligand-based active targeting mechanisms employing peptides, aptamers, and antibodies, we investigate how these nanocarriers are engineered for efficient tumor-targeted drug delivery. The review further delves into the understanding of nano-bio interactions (eg, size-dependent cellular uptake) and their interplay with cancer biology. We discuss how this knowledge, alongside the rational design of stimuli-responsive and multifunctional "smart" nanoplatforms, informs the development of more precise and effective therapeutic strategies. Finally, we address the ongoing challenges in clinical translation, such as patient heterogeneity and physiological barriers, and emphasize that comprehending these aspects is pivotal for guiding future translational research towards the realization of truly patient-centric nanomedicines.

Indexed as

active and passive targetingcancer therapydrug delivery systemsnanocarrierstargeted nanomedicine

Identifiers

PMID41098351
PMCPMC12520008

What OpenQuestion holds

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Registered trials

None linked

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.