Evidence map›Paper›PMID 41496895›Full record

ArticleThe journal of venomous animals and toxins including tropical diseases2025

Cnidarian toxins: omics approaches and recombinant proteins.

Jesús Eduardo Vega-Tamayo, Esteban de Jesús Alcantar-Orozco, Ramiro Arturo Mendoza-Ramírez, Luna Gabriela Silva-Díaz, Jorge Alberto Aguilar-Salazar, Diego Hermilo Salvador-Aguilar, Alejandra Rojas-Molina

Abstract read
In one paragraph

Article in The journal of venomous animals and toxins including tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Jesús Eduardo Vega-TamayoSchool of Chemistry, Autonomous University of Querétaro, Cerro de las Campanas, Querétaro, Qro, Mexico.ORCID https://orcid.org/0009-0000-6560-2086
Esteban de Jesús Alcantar-OrozcoSchool of Chemistry, Autonomous University of Querétaro, Cerro de las Campanas, Querétaro, Qro, Mexico.ORCID https://orcid.org/0009-0005-2743-3652
Ramiro Arturo Mendoza-RamírezSchool of Chemistry, Autonomous University of Querétaro, Cerro de las Campanas, Querétaro, Qro, Mexico.
Luna Gabriela Silva-DíazSchool of Chemistry, Autonomous University of Querétaro, Cerro de las Campanas, Querétaro, Qro, Mexico.
Jorge Alberto Aguilar-SalazarSchool of Chemistry, Autonomous University of Querétaro, Cerro de las Campanas, Querétaro, Qro, Mexico.
Diego Hermilo Salvador-AguilarSchool of Chemistry, Autonomous University of Querétaro, Cerro de las Campanas, Querétaro, Qro, Mexico.
Alejandra Rojas-MolinaSchool of Chemistry, Autonomous University of Querétaro, Cerro de las Campanas, Querétaro, Qro, Mexico.ORCID https://orcid.org/0000-0001-6131-9013

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cnidarian venom toxins have attracted increasing interest due to their remarkable molecular diversity and pharmacological potential. Omics technologies - such as genomics, transcriptomics, proteomics, and metabolomics - have facilitated the identification of toxin-encoding genes, providing key insights into their evolutionary trajectories and structure-function relationships, which are essential for understanding their mechanisms of action and therapeutic value. Nevertheless, the functional validation and production of complex toxins remain challenging, particularly for those requiring intricate folding or post-translational modifications. Recombinant expression has emerged as a strategic alternative to traditional purification methods, enabling controlled toxin production and the possibility of modifying their properties through genetic engineering. In parallel, advances in synthetic biology, such as cell-free protein synthesis systems, are creating new opportunities for toxin characterization, although their industrial scalability remains limited. Computational tools, including those based on artificial intelligence, are beginning to support the prioritization and functional analysis of toxins identified through omics approaches. This review provides an updated overview of the advances, limitations, and future perspectives in cnidarian toxin research, highlighting their promising role as a valuable source of bioactive compounds with therapeutic and biotechnological applications.

Indexed as

CnidariansOmics sciencesRecombinant proteinsToxins

Identifiers

PMID41496895
PMCPMC12767216

What OpenQuestion 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 OpenQuestion graph.