Evidence map›Paper›PMID 33449292›Full record

ArticleMedical oncology (Northwood, London, England)2021

Combined crizotinib and endocrine drugs inhibit proliferation, migration, and colony formation of breast cancer cells via downregulation of MET and estrogen receptor.

Nehad M Ayoub, Amer E Alkhalifa, Dalia R Ibrahim, Ahmed Alhusban

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. The Impact of the Coexpression ofThe breast journal · 2024
    Article
  2. Article
  3. Article
  4. Receptor tyrosine kinase inhibitors in cancer.Cellular and molecular life sciences : CMLS · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. 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

4 authors at 1 institution in 1 country.

Nehad M AyoubDepartment of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology (JUST), Irbid, 22110, Jordan. nmayoub@just.edu.jo.ORCID http://orcid.org/0000-0002-6643-8553
Amer E AlkhalifaDepartment of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology (JUST), Irbid, 22110, Jordan.
Dalia R IbrahimDepartment of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology (JUST), Irbid, 22110, Jordan.
Ahmed AlhusbanDepartment of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology (JUST), Irbid, 22110, Jordan.
Jordan University of Science and Technology · JO

Funding

Deanship of Research, Jordan University of Science and Technology 20180279
6 · The paper itself

Abstract

Hormone-dependent breast cancer is the most abundant molecular subtype of the disease. Despite the availability of endocrine treatments, the use of these drugs is limited by their serious adverse reactions and development of acquired resistance often mediated by growth factor receptors. The hepatocyte growth factor receptor, MET, is a receptor tyrosine kinase known for its oncogenic activity and mediating resistance to targeted therapies. Crizotinib is a small-molecule tyrosine kinase inhibitor of MET. In this study, the anticancer effects of combined crizotinib and endocrine drugs were investigated in breast cancer cells in vitro along with the molecular mechanisms associated with these effects. Results showed that crizotinib inhibited growth of MCF7 and T-47D breast cancer cells in a dose-dependent manner with IC

Indexed as

Antineoplastic Agents, HormonalBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationCrizotinibDrug SynergismEstrogen Receptor alphaFulvestrantHumansInhibitory Concentration 50Ki-67 AntigenProtein Kinase InhibitorsProto-Oncogene Proteins c-metTamoxifenafimoxifeneAntineoplastic Agents, HormonalCrizotinibEstrogen Receptor alphaFulvestrantKi-67 AntigenMET protein, humanMKI67 protein, humanProtein Kinase InhibitorsProto-Oncogene Proteins c-metTamoxifenBreast cancerCrizotinibEstrogen receptorMETSynergismTamoxifen

Identifiers

PMID33449292
OpenAlexW3120763681

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.