Evidence map›Paper›PMID 41541913›Full record

ReviewCancer pathogenesis and therapy2026

Arthropod venom peptides: Pioneering nanotechnology in cancer treatment and drug delivery.

Sara K Ghodeif, Nadia A El-Fahla, Mohamed A Abdel-Rahman, Nahla S El-Shenawy

Abstract readReview
In one paragraph

Review in Cancer pathogenesis and therapy, 2026. 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. Evaluation of the Cytotoxic Effects ofJournal of arthropod-borne diseases · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
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

4 authors.

Sara K GhodeifZoology Department, Faculty of Science, Suez Canal University, Ismailia, 41522, Egypt.
Nadia A El-FahlaZoology Department, Faculty of Science, Suez Canal University, Ismailia, 41522, Egypt.
Mohamed A Abdel-RahmanZoology Department, Faculty of Science, Suez Canal University, Ismailia, 41522, Egypt.
Nahla S El-ShenawyZoology Department, Faculty of Science, Suez Canal University, Ismailia, 41522, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is the second leading cause of death globally, claiming >10 million lives in 2020 and a projected increase to 13 million by 2030. Traditional treatments such as chemotherapy, radiation, and surgery can be effective but often lead to systemic toxicity and drug conflict due to their lack of selectivity. Nanotechnology is a promising alternative that targets cancer cells and reduces harm to healthy tissues. We aimed to conduct a review to present an inclusive examination of nanotechnology, macromolecules, and related methodologies, focusing on therapeutic strategies utilizing arthropod venom peptides and nanotechnological approaches. Nanoparticles (NPs) ranging from 1 to 100 nm improve drug delivery and treatment outcomes by enhancing bioavailability, controlling drug release, and exploiting tumor-specific features. However, biocompatibility, manufacturing complexity, and regulatory hurdles have hindered their widespread clinical use. Arthropod venom contains bioactive compounds that primarily target ion channels, which play a role in cancer progression. Venom-derived peptides are emerging as promising anticancer agents, and nanotechnology offers an effective strategy for their delivery. NPs have enhanced therapeutic potential by improving controlled release, stability, and cellular uptake while minimizing toxicity. Liposomal- and lipid-based NPs and organic carriers such as chitosan show particular promise for targeted drug delivery. Combining nanotechnology with venom-derived peptides, particularly those from arthropods such as scorpions, may enhance the selectivity and efficacy of cancer treatments. These peptides selectively target cancer cells, minimize toxicity, and improve therapeutic outcomes. This review highlights the potential of venom-derived peptides combined with NPs in cancer therapy, as well as their benefits, challenges, and future research directions for innovative treatment approaches. Future studies should focus on optimizing venom peptide formulations with NPs to enhance efficacy, reduce systemic toxicity, and develop safer and more effective cancer treatments.

Indexed as

AnticancerArthropodsDrug deliveryNanotechnologyVenom peptide

Identifiers

PMID41541913
PMCPMC12800701

What OpenQuestion holds

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Registered trials

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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.