Evidence map›Paper›PMID 35768871›Full record

ArticleMolecular cancer2022

Ceritinib is a novel triple negative breast cancer therapeutic agent.

Shengli Dong, Hassan Yousefi, Isabella Van Savage, Samuel C Okpechi, Maryl K Wright, Margarite D Matossian, Bridgette M Collins-Burow, Matthew E Burow, Suresh K Alahari

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  7. Multi-omics profile of exceptional long-term survivors of AJCC stage III triple-negative breast cancer.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2025
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  16. YB-1 activating cascades as potential targets in KRAS-mutated tumors.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2023
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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 3 institutions in 1 country.

Shengli Dong *TYK Medicines, Inc, Zhejiang, People's Republic of China, 313100.
Hassan Yousefi *Department of Biochemistry and Molecular Biology, LSUHSC School of Medicine, New Orleans, LA, 70112, USA.
Isabella Van SavageTulane University School of Medicine, New Orleans, Louisiana, 70118, USA.
Samuel C OkpechiDepartment of Biochemistry and Molecular Biology, LSUHSC School of Medicine, New Orleans, LA, 70112, USA.
Maryl K WrightTulane University School of Medicine, New Orleans, Louisiana, 70118, USA.
Margarite D MatossianDepartment of Medicine, The University of Chicago, Chicago, IL, 60637, USA.
Bridgette M Collins-BurowTulane University School of Medicine, New Orleans, Louisiana, 70118, USA.
Matthew E BurowTulane University School of Medicine, New Orleans, Louisiana, 70118, USA.
Suresh K AlahariDepartment of Biochemistry and Molecular Biology, LSUHSC School of Medicine, New Orleans, LA, 70112, USA. salaha@lsuhsc.edu.ORCID 0000-0002-9651-6727
Louisiana State University Health Sciences Center New Orleans · USTulane University · USUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTriple-negative breast cancers (TNBCs) are clinically aggressive subtypes of breast cancer. TNBC is difficult to treat with targeted agents due to the lack of commonly targeted therapies within this subtype. Androgen receptor (AR) has been detected in 12-55% of TNBCs. AR stimulates breast tumor growth in the absence of estrogen receptor (ER), and it has become an emerging molecular target in TNBC treatment.

methodsCeritinib is a small molecule inhibitor of tyrosine kinase and it is used in the therapy of non-small lung cancer patients. Enzalutamide is a small molecule compound targeting the androgen receptor and it is used to treat prostate cancer. Combination therapy of these drugs were investigated using AR positive breast cancer mouse xenograft models. Also, combination treatment of ceritinib and paclitaxel investigated using AR

resultsWe screened 133 FDA approved drugs that have a therapeutic effect of AR

conclusionsTo improve the response of AR antagonist in AR positive TNBC, we designed a novel combinational strategy comprised of enzalutamide and ceritinib to treat AR

Indexed as

Triple Negative Breast NeoplasmsAndrogensAnimalsCell Line, TumorHumansMicePaclitaxelPyrimidinesReceptors, AndrogenSulfonesAndrogensceritinibPaclitaxelPyrimidinesReceptors, AndrogenSulfonesAndrogen receptorCeritinibEnzalutamidePaclitaxelRTK/ACK/AR

Identifiers

PMID35768871
PMCPMC9241294
OpenAlexW4283697159

What OpenQuestion holds

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Registered trials

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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.