Evidence map›Paper›PMID 41155199›Full record

ReviewInternational journal of molecular sciences2025

Scorpion Venom as a Source of Cancer Drugs: A Comprehensive Proteomic Analysis and Therapeutic Potential.

Stephanie Santos Suehiro Arcos, Mariana Ramos da Cunha Aguiar, Júlia de Oliveira, Matheus Ramos da Silva, Isabela de Oliveira Cavalcante Pimentel, Nicolas Gamboa Dos Anjos, Gustavo Henrique Rohr Souza Machado, Kimberly Borges Evangelista, Fernanda Calheta Vieira Portaro, Leo Kei Iwai

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Review
  6. 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

10 authors.

Stephanie Santos Suehiro ArcosLaboratory of Applied Toxinology (LETA) and Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo 05503-900, Brazil.
Mariana Ramos da Cunha AguiarLaboratory of Applied Toxinology (LETA) and Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo 05503-900, Brazil.
Júlia de OliveiraLaboratory of Applied Toxinology (LETA) and Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo 05503-900, Brazil.
Matheus Ramos da SilvaLaboratory of Applied Toxinology (LETA) and Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo 05503-900, Brazil.
Isabela de Oliveira Cavalcante PimentelLaboratory of Applied Toxinology (LETA) and Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo 05503-900, Brazil.
Nicolas Gamboa Dos AnjosLaboratory of Applied Toxinology (LETA) and Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo 05503-900, Brazil.
Gustavo Henrique Rohr Souza MachadoLaboratory of Applied Toxinology (LETA) and Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo 05503-900, Brazil.
Kimberly Borges EvangelistaLaboratory of Applied Toxinology (LETA) and Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo 05503-900, Brazil.
Fernanda Calheta Vieira PortaroLaboratory of Structure and Functions of Biomolecules, Butantan Institute, São Paulo 05503-900, Brazil.ORCID 0000-0002-9582-4699
Leo Kei IwaiLaboratory of Applied Toxinology (LETA) and Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo 05503-900, Brazil.ORCID 0000-0002-1571-7763

Funding

CAPES 88887.804166/2023-00, 88882.442313/2019-01CNPq 131408/2019-4FAPESP 2024/16166-0, 2019/20832-7, 2017/17943-6, 2016/04000-3, 2013/07467-1
6 · The paper itself

Abstract

Scorpion venom is a rich source of bioactive compounds with significant potential for anticancer drug development. Its diverse molecular composition, including neurotoxins, antimicrobial peptides, and enzymes, provides a vast library for therapeutic innovation. Proteomic analyses have characterized venom composition in several species, while further functional assays have clarified their anticancer mechanisms. This review synthesizes current knowledge on scorpion venom-derived peptides with demonstrated anticancer activity, which selectively target ion channels, induce apoptosis, or disrupt tumor microenvironments. Where available, we highlight proteomic studies that have identified these components and discuss their structural features relevant to drug design. We also examine clinical applications and the challenges in translating venom peptides into therapies. The crucial and growing role of proteomics in this field, particularly for venom fractionation, component identification, and structural characterization, is critically evaluated.

Indexed as

Antineoplastic AgentsNeoplasmsProteomicsScorpion VenomsAnimalsHumansPeptidesScorpionsAntineoplastic AgentsPeptidesScorpion Venomsanticancer peptidescancerdrug deliverynatural productsproteomicsscorpion venomtargeted therapy

Identifiers

PMID41155199
PMCPMC12564133

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.