Evidence map›Paper›PMID 30318506›Full record

ArticleBritish journal of cancer2018

An IL13Rα2 peptide exhibits therapeutic activity against metastatic colorectal cancer.

Rubén A Bartolomé, Marta Jaén, J Ignacio Casal

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

27 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Biological Activity of Natural and Synthetic Peptides as Anticancer Agents.International journal of molecular sciences · 2024
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Annals of nuclear medicine · 2022
    Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Involvement of IL-4, IL-13 and Their Receptors in Pancreatic Cancer.International journal of molecular sciences · 2021
    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

3 authors at 1 institution in 1 country.

Rubén A BartoloméDepartment of Molecular Biomedicine, Centro de Investigaciones Biológicas, CSIC, Ramiro de Maeztu 9, 28039, Madrid, Spain.
Marta JaénDepartment of Molecular Biomedicine, Centro de Investigaciones Biológicas, CSIC, Ramiro de Maeztu 9, 28039, Madrid, Spain.
J Ignacio CasalDepartment of Molecular Biomedicine, Centro de Investigaciones Biológicas, CSIC, Ramiro de Maeztu 9, 28039, Madrid, Spain. icasal@cib.csic.es.ORCID http://orcid.org/0000-0003-1085-2840
Centro de Investigaciones Biológicas Margarita Salas · ES

Funding

Ministerio de Economía y Competitividad (Ministry of Economy and Competitiveness) BIO2015-66489-RMinistry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) IPT13/0001-ISCIII-SGEFI/FEDER
6 · The paper itself

Abstract

backgroundInterleukin 13 receptor α2 (IL13Rα2) is overexpressed in metastatic colorectal cancer. Here, we have developed novel strategies to block IL-13 binding to IL13Rα2 in order to reduce metastatic spread.

methodsSynthetic IL13Rα2 D1 peptide (GSETWKTIITKN) was tested for the inhibition of IL-13 binding to IL13Rα2 using ELISA and different cellular assays. Peptide blocking effects on different cell signalling mediators were determined by western blot. An enantiomer version of the peptide (D-D1) was prepared to avoid proteolytic digestion. Nude mice were used for tumour growth and survival analysis after treatment with IL13Rα2 peptides.

resultsIL13Rα2 D1 peptide inhibited migration, invasion, and proliferation in metastatic colorectal and glioblastoma cancer cells treated with IL-13. Residues

conclusionsWe propose that the D-D1 peptide from IL13Rα2 represents a promising therapeutic agent to inhibit metastatic progression in colorectal cancer and, likely, other solid tumours.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsFocal Adhesion Kinase 1GlioblastomaHT29 CellsHumansInterleukin-13Interleukin-13 Receptor alpha2 SubunitMatrix Metalloproteinase 14MiceMice, NudePhosphatidylinositol 3-KinasesAntineoplastic AgentsFocal Adhesion Kinase 1IL13RA2 protein, humanInterleukin-13Interleukin-13 Receptor alpha2 SubunitMatrix Metalloproteinase 14Mmp14 protein, mousePhosphatidylinositol 3-KinasesPtk2 protein, mouseRNA, Small InterferingStat6 protein, mouseSTAT6 Transcription Factor

Identifiers

PMID30318506
PMCPMC6203792
OpenAlexW2897971744

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.