Evidence map›Paper›PMID 33490071›Full record

ArticleFrontiers in cell and developmental biology2020

Loss of G-Protein Pathway Suppressor 2 Promotes Tumor Growth Through Activation of AKT Signaling.

Stefanie Chan, Emma Smith, Yuan Gao, Julian Kwan, Benjamin C Blum, Andrew M Tilston-Lunel, Isabella Turcinovic, Xaralabos Varelas, Maria Dafne Cardamone, Stefano Monti and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

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  12. Targeting Akt in cancer for precision therapy.Journal of hematology & oncology · 2021
    Review
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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

12 authors at 2 institutions in 1 country.

Stefanie ChanDepartment of Biochemistry, Boston University School of Medicine, Boston, MA, United States.
Emma SmithDepartment of Biochemistry, Boston University School of Medicine, Boston, MA, United States.
Yuan GaoDepartment of Biochemistry, Boston University School of Medicine, Boston, MA, United States.
Julian KwanCenter for Network Systems Biology, Boston University, Boston, MA, United States.
Benjamin C BlumCenter for Network Systems Biology, Boston University, Boston, MA, United States.
Andrew M Tilston-LunelDepartment of Biochemistry, Boston University School of Medicine, Boston, MA, United States.
Isabella TurcinovicCenter for Network Systems Biology, Boston University, Boston, MA, United States.
Xaralabos VarelasDepartment of Biochemistry, Boston University School of Medicine, Boston, MA, United States.
Maria Dafne CardamoneDepartment of Biochemistry, Boston University School of Medicine, Boston, MA, United States.
Stefano MontiDivision of Computational Biology, Department of Medicine, Boston University School of Medicine, Boston, MA, United States.
Andrew EmiliDepartment of Biochemistry, Boston University School of Medicine, Boston, MA, United States.
Valentina PerissiDepartment of Biochemistry, Boston University School of Medicine, Boston, MA, United States.
Boston University · USCenter for Systems Biology · US

Funding

Regulation of mitochondrial homeostasis through retrograde signalingR01GM127625 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI PERISSI, VALENTINA · 2018 to 2021
$1.8M
NIGMS NIH HHS R01 GM127625
6 · The paper itself

Abstract

G Protein Suppressor 2 (GPS2) is a multifunctional protein that exerts important roles in inflammation and metabolism in adipose, liver, and immune cells. GPS2 has recently been identified as a significantly mutated gene in breast cancer and other malignancies and proposed to work as a putative tumor suppressor. However, molecular mechanisms by which GPS2 prevents cancer development and/or progression are largely unknown. Here, we have profiled the phenotypic changes induced by GPS2 depletion in MDA-MB-231 triple negative breast cancer cells and investigated the underlying molecular mechanisms. We found that GPS2-deleted MDA-MB-231 cells exhibited increased proliferative, migratory, and invasive properties

Indexed as

Aktbreast cancerGPS2MK2206 (PubChem CID: 46930998)ubiquitin (Ub)

Identifiers

PMID33490071
PMCPMC7817781
OpenAlexW3120044287

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.