Evidence map›Paper›PMID 32333142›Full record

ArticleJournal of cancer research and clinical oncology2020

Afatinib is active in osteosarcoma in osteosarcoma cell lines.

Marlid Cruz-Ramos, Yessica Zamudio-Cuevas, Daniel Medina-Luna, Karina Martínez-Flores, Gabriela Martínez-Nava, Javier Fernández-Torres, Alberto López-Reyes, Flavio Solca

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 4 countries.

Marlid Cruz-Ramos *Oncology Translational Laboratory, Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain. marlid.cruz@gmail.com.
Yessica Zamudio-Cuevas *Laboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación, Mexico City, CDMX, México.
Daniel Medina-LunaLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación, Mexico City, CDMX, México.
Karina Martínez-FloresLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación, Mexico City, CDMX, México.
Gabriela Martínez-NavaLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación, Mexico City, CDMX, México.
Javier Fernández-TorresLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación, Mexico City, CDMX, México.
Alberto López-ReyesLaboratorio de Gerociencias, Instituto Nacional de Rehabilitación, Mexico City, CDMX, México.
Flavio SolcaBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Instituto Nacional de Rehabilitación · MXBoehringer Ingelheim (Austria) · ATHospital Universitario Fundación Jiménez Díaz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOsteosarcoma is the most common bone tumor, mainly affecting adolescents and young adults, and metastatic disease has poor outcomes with a dismal overall survival. Currently, chemotherapy is the standard of care with limited results, finding that new therapies could improve these outcomes. Preclinical and clinical studies have suggested a possible important role of ErbB pathway aberrations in osteosarcoma etiology. The present study shows the effect of afatinib, an irreversible ErbB family blocker in osteosarcoma cell lines.

methodsWithin a panel of human osteosarcoma cell lines, we addressed cell viability assay using afatinib at increasing concentrations. Motility was measured in wound-healing assays and invasion capacity was assessed in Transwell chamber assays. Finally, to monitor ErbB pathway modulation by afatinib and related compounds, we used Western blot analyses.

resultsCell viability inhibition, as well as a reduction of motility and migration of osteosarcoma cell line were observed after treatment with afatinib. Likewise, in the HOS cell line, afatinib decreased phosphorylation of key components in the ErbB signaling pathway.

conclusionsAfatinib shows relevant antitumor effect in several osteosarcoma cell lines, as it causes a significant impact on cell viability, motility, and migration with a significant decrease in the activation of ErbB pathway activity.

Indexed as

AfatinibAnimalsAntineoplastic AgentsCell Line, TumorCell MovementCell ProliferationCell SurvivalDisease Models, AnimalDose-Response Relationship, DrugErb-b2 Receptor Tyrosine KinasesErbB ReceptorsHumansOsteosarcomaProtein Kinase InhibitorsXenograft Model Antitumor AssaysAfatinibAntineoplastic AgentsEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsProtein Kinase InhibitorsAfatinibAntitumoralErbBOsteosarcoma

Identifiers

PMID32333142
PMCPMC11804738
OpenAlexW3018446798

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.