Evidence map›Paper›PMID 33198314›Full record

ReviewInternational journal of molecular sciences2020

Tyrosine Kinase Receptors in Oncology.

Jorge Esteban-Villarrubia, Juan José Soto-Castillo, Javier Pozas, María San Román-Gil, Inmaculada Orejana-Martín, Javier Torres-Jiménez, Alfredo Carrato, Teresa Alonso-Gordoa, Javier Molina-Cerrillo

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 4% 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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 95 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. A Constellation of Fluorescent Biosensors to Illuminate the Galaxy of Protein Kinases.Chembiochem : a European journal of chemical biology · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
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  18. Article
  19. Expression of MutatedVeterinary sciences · 2024
    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

9 authors at 2 institutions in 1 country.

Jorge Esteban-VillarrubiaMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain.
Juan José Soto-CastilloMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain.ORCID 0000-0001-9630-4233
Javier PozasMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain.
María San Román-GilMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain.
Inmaculada Orejana-MartínMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain.
Javier Torres-JiménezMedical Oncology Department, University Hospital Ramon y Cajal, 28034 Madrid, Spain.ORCID 0000-0001-9023-4529
Alfredo CarratoMedical Oncology Department, Ramón y Cajal Health Research Institute (IRYCIS), CIBERONC, Alcalá University, University Hospital Ramon y Cajal, 28034 Madrid, Spain.ORCID 0000-0001-7749-8140
Teresa Alonso-GordoaMedical Oncology Department, Ramón y Cajal Health Research Institute (IRYCIS), CIBERONC, Alcalá University, University Hospital Ramon y Cajal, 28034 Madrid, Spain.ORCID 0000-0002-8966-7236
Javier Molina-CerrilloMedical Oncology Department, Ramón y Cajal Health Research Institute (IRYCIS), CIBERONC, Alcalá University, University Hospital Ramon y Cajal, 28034 Madrid, Spain.ORCID 0000-0003-4616-0598
Hospital Universitario Ramón y Cajal · ESInstituto Cajal · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tyrosine kinase receptors (TKR) comprise more than 60 molecules that play an essential role in the molecular pathways, leading to cell survival and differentiation. Consequently, genetic alterations of TKRs may lead to tumorigenesis and, therefore, cancer development. The discovery and improvement of tyrosine kinase inhibitors (TKI) against TKRs have entailed an important step in the knowledge-expansion of tumor physiopathology as well as an improvement in the cancer treatment based on molecular alterations over many tumor types. The purpose of this review is to provide a comprehensive review of the different families of TKRs and their role in the expansion of tumor cells and how TKIs can stop these pathways to tumorigenesis, in combination or not with other therapies. The increasing growth of this landscape is driving us to strengthen the development of precision oncology with clinical trials based on molecular-based therapy over a histology-based one, with promising preliminary results.

Indexed as

Anaplastic Lymphoma KinaseCarcinogenesisErb-b2 Receptor Tyrosine KinasesErbB ReceptorsHumansImmunotherapyLigandsNeoplasmsNeovascularization, PathologicPhosphorylationPrecision MedicineProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-kitReceptor, Fibroblast Growth Factor, Type 1Receptor Protein-Tyrosine KinasesALK protein, humanAnaplastic Lymphoma KinaseEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFGFR1 protein, humanKIT protein, humanLigandsNTRK1 protein, humanProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-kitReceptor, Fibroblast Growth Factor, Type 1Receptor Protein-Tyrosine KinasesReceptor, trkAROS1 protein, humanresearchtumorigenesistyrosine kinase receptor inhibitorstyrosine kinase receptors

Identifiers

PMID33198314
PMCPMC7696731
OpenAlexW3098654009

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.