Evidence map›Paper›PMID 30200768›Full record

ArticleJournal of proteome research2018

Quantitative Proteomic Profiling Reveals Key Pathways in the Anticancer Action of Methoxychalcone Derivatives in Triple Negative Breast Cancer.

Catherine C Going, Dhanir Tailor, Vineet Kumar, Alisha M Birk, Mallesh Pandrala, Meghan A Rice, Tanya Stoyanova, Sanjay Malhotra, Sharon J Pitteri

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

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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 1 institution in 1 country.

Catherine C GoingDepartment of Radiology, Canary Center at Stanford for Cancer Early Detection , Stanford University School of Medicine , Palo Alto , California 94304 , United States.
Dhanir TailorDepartment of Radiation Oncology , Stanford University School of Medicine , Palo Alto , California 94304 , United States.
Vineet KumarDepartment of Radiation Oncology , Stanford University School of Medicine , Palo Alto , California 94304 , United States.
Alisha M BirkDepartment of Radiology, Canary Center at Stanford for Cancer Early Detection , Stanford University School of Medicine , Palo Alto , California 94304 , United States.
Mallesh PandralaDepartment of Radiation Oncology , Stanford University School of Medicine , Palo Alto , California 94304 , United States.
Meghan A RiceDepartment of Radiology, Canary Center at Stanford for Cancer Early Detection , Stanford University School of Medicine , Palo Alto , California 94304 , United States.
Tanya StoyanovaDepartment of Radiology, Canary Center at Stanford for Cancer Early Detection , Stanford University School of Medicine , Palo Alto , California 94304 , United States.
Sanjay MalhotraDepartment of Radiology, Canary Center at Stanford for Cancer Early Detection , Stanford University School of Medicine , Palo Alto , California 94304 , United States.
Sharon J PitteriDepartment of Radiology, Canary Center at Stanford for Cancer Early Detection , Stanford University School of Medicine , Palo Alto , California 94304 , United States.ORCID 0000-0002-3119-873X
Stanford University · US

Funding

Proteolytically Cleaved Receptors as Oncogenes and Therapeutic TargetsR00CA184397 · NCI · STANFORD UNIVERSITY · PI STOYANOVA, TANYA I · 2016 to 2018
$729k
Elucidating Novel Mechanisms Underlying Prostate Cancer DevelopmentR03CA230819 · NCI · STANFORD UNIVERSITY · PI STOYANOVA, TANYA I · 2018 to 2019
$160k
NCI NIH HHS R00 CA184397
6 · The paper itself

Abstract

Triple negative breast cancer is an aggressive, heterogeneous disease with high recurrence and metastasis rates even with modern chemotherapy regimens and thus is in need of new therapeutics. Here, three novel synthetic analogues of chalcones, plant-based molecules that have demonstrated potency against a wide variety of cancers, were investigated as potential therapeutics for triple negative breast cancer. These compounds exhibit IC

Indexed as

Antineoplastic AgentsApoptosisCell LineCell Line, TumorCell ProliferationChalconeFemaleG1 Phase Cell Cycle CheckpointsHumansMetabolic Networks and PathwaysProteomicsTriple Negative Breast NeoplasmsAntineoplastic AgentsChalconechalconemechanism of actiontandem mass tag (TMT)triple negative breast cancerunfolded protein response

Identifiers

PMID30200768
PMCPMC8078626
OpenAlexW2890118867

What OpenQuestion holds

Textmetadata
LicenceTDM
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.