Evidence map›Paper›PMID 27010507›Full record

ReviewProtein science : a publication of the Protein Society2016

From amino acid sequence to bioactivity: The biomedical potential of antitumor peptides.

Aitor Blanco-Míguez, Alberto Gutiérrez-Jácome, Martín Pérez-Pérez, Gael Pérez-Rodríguez, Sandra Catalán-García, Florentino Fdez-Riverola, Anália Lourenço, Borja Sánchez

Open access · bronzeAbstract readReview
In one paragraph

Review in Protein science : a publication of the Protein Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.7field-weighted citation impact, top 7% of its field
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

32 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Peptide-Based Therapeutics in Cancer Therapy.Molecular biotechnology · 2024
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Peptides as multifunctional players in cancer therapy.Experimental & molecular medicine · 2023
    Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. 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 at 4 institutions in 2 countries.

Aitor Blanco-MíguezESEI - Escuela Superior De Ingeniería Informática, Edificio Politécnico, Campus Universitario as Lagoas S/N, Universidad De Vigo, Ourense, 32004, Spain.
Alberto Gutiérrez-JácomeESEI - Escuela Superior De Ingeniería Informática, Edificio Politécnico, Campus Universitario as Lagoas S/N, Universidad De Vigo, Ourense, 32004, Spain.
Martín Pérez-PérezESEI - Escuela Superior De Ingeniería Informática, Edificio Politécnico, Campus Universitario as Lagoas S/N, Universidad De Vigo, Ourense, 32004, Spain.
Gael Pérez-RodríguezESEI - Escuela Superior De Ingeniería Informática, Edificio Politécnico, Campus Universitario as Lagoas S/N, Universidad De Vigo, Ourense, 32004, Spain.
Sandra Catalán-GarcíaAsturias, INDRA Software Labs, C/Jimena Fernández De La Vega, 140 P. Científico Tecnológico, Ed, Gijón, 33203, Spain.
Florentino Fdez-RiverolaESEI - Escuela Superior De Ingeniería Informática, Edificio Politécnico, Campus Universitario as Lagoas S/N, Universidad De Vigo, Ourense, 32004, Spain.
Anália LourençoESEI - Escuela Superior De Ingeniería Informática, Edificio Politécnico, Campus Universitario as Lagoas S/N, Universidad De Vigo, Ourense, 32004, Spain.
Borja SánchezDepartment of Microbiology and Biochemistry of Dairy Products, Instituto De Productos Lácteos De Asturias (IPLA), Consejo Superior De Investigaciones Científicas (CSIC), Villaviciosa, Asturias, Spain.
Universidade de Vigo · ESInstituto de Productos Lácteos de Asturias · ESSoftware (Spain) · ESUniversity of Minho · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemoprevention is the use of natural and/or synthetic substances to block, reverse, or retard the process of carcinogenesis. In this field, the use of antitumor peptides is of interest as, (i) these molecules are small in size, (ii) they show good cell diffusion and permeability, (iii) they affect one or more specific molecular pathways involved in carcinogenesis, and (iv) they are not usually genotoxic. We have checked the Web of Science Database (23/11/2015) in order to collect papers reporting on bioactive peptide (1691 registers), which was further filtered searching terms such as "antiproliferative," "antitumoral," or "apoptosis" among others. Works reporting the amino acid sequence of an antiproliferative peptide were kept (60 registers), and this was complemented with the peptides included in CancerPPD, an extensive resource for antiproliferative peptides and proteins. Peptides were grouped according to one of the following mechanism of action: inhibition of cell migration, inhibition of tumor angiogenesis, antioxidative mechanisms, inhibition of gene transcription/cell proliferation, induction of apoptosis, disorganization of tubulin structure, cytotoxicity, or unknown mechanisms. The main mechanisms of action of those antiproliferative peptides with known amino acid sequences are presented and finally, their potential clinical usefulness and future challenges on their application is discussed.

Indexed as

Antineoplastic AgentsDatabases, ProteinNeoplasmsNeovascularization, PathologicPeptidesAnimalsCell MovementCell ProliferationHumansAntineoplastic AgentsPeptidesantiproliferativeantitumoralbioactive peptidecancertumor

Identifiers

PMID27010507
PMCPMC4941772
OpenAlexW2418939562

What OpenQuestion holds

Textmetadata
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.