Evidence map›Paper›PMID 21817116›Full record

ArticleMolecular cancer therapeutics2011

Identification of a natural compound by cell-based screening that enhances interferon regulatory factor-1 activity and causes tumor suppression.

Jinbo Gao, Yujun Wang, Quanhua Xing, Jin Yan, Maheswari Senthil, Yasir Akmal, Claudia M Kowolik, Julia Kang, David M Lu, Ming Zhao and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 19 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

14 authors at 6 institutions in 2 countries.

Jinbo GaoDepartment of Surgery, Union Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, PR China.
Yujun Wang
Quanhua Xing
Jin Yan
Maheswari Senthil
Yasir Akmal
Claudia M Kowolik
Julia Kang
David M Lu
Ming Zhao
Zhixiu Lin
Christopher H K Cheng
M L Richard Yip
John H Yim
City Of Hope National Medical Center · USLoma Linda University · USChinese University of Hong Kong · CNHuazhong University of Science and Technology · CNUnion Hospital · CNCity of Hope · US

Funding

Role of IRF-1 in Tumor Suppression of Breast CancerK08CA098403 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI YIM, JOHN H · 2004 to 2008
$660k
NCI NIH HHS K08 CA098403NCI NIH HHS K08CA098403
6 · The paper itself

Abstract

The transcription factor interferon regulatory factor-1 (IRF-1) is induced by many tumor-suppressive stimuli and can mediate antiproliferative and proapoptotic effects in cancer cells. Thus, identifying agents that enhance IRF-1 activity may be an effective approach to cancer therapy. A cell-based screening assay was developed to identify extracts and compounds that could enhance IRF-1 activity, using an IRF-1-dependent luciferase reporter cell line. Through this approach, we identified a natural product extract and a known active component of this extract, baicalein, which causes a marked increase in IRF-1-dependent reporter gene expression and IRF-1 protein, with modulation of known IRF-1 targets PUMA and cyclin D1. Baicalein causes suppression of growth in vitro in multiple cancer cell lines in the low micromolar range. IRF-1 plays a role in this growth suppression as shown by significant resistance to growth suppression in a breast cancer cell line stably transfected with short hairpin RNA against IRF-1. Finally, intraperitoneal administration of baicalein by repeated injection causes inhibition of growth in both xenogeneic and syngeneic mouse models of cancer without toxicity to the animals. These findings indicate that identifying enhancers of IRF-1 activity may have utility in anticancer therapies and that cell-based screening for activation of transcription factors can be a useful approach for drug discovery.

Indexed as

AnimalsCell Growth ProcessesCell Line, TumorDisease Models, AnimalFemaleFlavanonesHumansInterferon Regulatory Factor-1MiceMice, SCIDNeoplasmsRandom AllocationTranscription FactorsTransfectionUp-RegulationXenograft Model Antitumor AssaysbaicaleinFlavanonesInterferon Regulatory Factor-1IRF1 protein, humanTranscription Factors

Identifiers

PMID21817116
PMCPMC3191301
OpenAlexW2152799867

What OpenQuestion holds

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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.