Evidence map›Paper›PMID 30655532›Full record

ArticleNature communications2019

Characterization of the Src-regulated kinome identifies SGK1 as a key mediator of Src-induced transformation.

Xiuquan Ma, Luxi Zhang, Jiangning Song, Elizabeth Nguyen, Rachel S Lee, Samuel J Rodgers, Fuyi Li, Cheng Huang, Ralf B Schittenhelm, Howard Chan and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

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  12. Discovery of Herbacetin as a Novel SGK1 Inhibitor to Alleviate Myocardial Hypertrophy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
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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

16 authors at 5 institutions in 3 countries.

Xiuquan MaCancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.ORCID http://orcid.org/0000-0001-7227-1289
Luxi ZhangCancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.
Jiangning SongDepartment of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC, 3800, Australia.ORCID http://orcid.org/0000-0001-8031-9086
Elizabeth NguyenCancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.
Rachel S LeeCancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.
Samuel J RodgersCancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.
Fuyi LiDepartment of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC, 3800, Australia.
Cheng HuangMonash Biomedical Proteomics Facility and Monash Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.
Ralf B SchittenhelmMonash Biomedical Proteomics Facility and Monash Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.
Howard ChanCancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.
Chanly ChheangCancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.
Jianmin WuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Centre for Cancer Bioinformatics, Peking University Cancer Hospital & Institute, Beijing, 100142, China.ORCID http://orcid.org/0000-0002-8876-128X
Kristin K BrownCancer Therapeutics Program and Cancer Metabolism Program, Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia.
Christina A MitchellCancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.
Kaylene J SimpsonSir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC, 3010, Australia.
Roger J DalyCancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia. roger.daly@monash.edu.
Australian Regenerative Medicine Institute · AUDiscovery Institute · USMonash University · AUThe University of Melbourne · AUPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite significant progress, our understanding of how specific oncogenes transform cells is still limited and likely underestimates the complexity of downstream signalling events. To address this gap, we use mass spectrometry-based chemical proteomics to characterize the global impact of an oncogene on the expressed kinome, and then functionally annotate the regulated kinases. As an example, we identify 63 protein kinases exhibiting altered expression and/or phosphorylation in Src-transformed mammary epithelial cells. An integrated siRNA screen identifies nine kinases, including SGK1, as being essential for Src-induced transformation. Accordingly, we find that Src positively regulates SGK1 expression in triple negative breast cancer cells, which exhibit a prominent signalling network governed by Src family kinases. Furthermore, combined inhibition of Src and SGK1 reduces colony formation and xenograft growth more effectively than either treatment alone. Therefore, this approach not only provides mechanistic insights into oncogenic transformation but also aids the design of improved therapeutic strategies.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntineoplastic AgentsBenzodioxolesCell Line, TumorCell Transformation, NeoplasticFemaleGene Knockdown TechniquesHEK293 CellsHumansImmediate-Early ProteinsMass SpectrometryMice, Inbred BALB CMice, NudeOncogenesProtein Interaction MappingAntineoplastic AgentsBenzodioxolesImmediate-Early ProteinsProtein Serine-Threonine KinasesQuinazolinesRNA, Small InterferingsaracatinibSerum-Glucocorticoid Regulated Kinasessrc-Family Kinases

Identifiers

PMID30655532
PMCPMC6336867
OpenAlexW2908941326

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.