Evidence map›Paper›PMID 24521094›Full record

ArticleCell communication and signaling : CCS2014

G(i)α proteins exhibit functional differences in the activation of ERK1/2, Akt and mTORC1 by growth factors in normal and breast cancer cells.

Zhanwei Wang, Rica Dela Cruz, Fang Ji, Sheng Guo, Jianhua Zhang, Ying Wang, Gen-Sheng Feng, Lutz Birnbaumer, Meisheng Jiang, Wen-Ming Chu

Open access · goldAbstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2014. 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
0.9field-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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  4. Protective effects of GαNaunyn-Schmiedeberg's archives of pharmacology · 2024
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  6. SCF/c-Kit-activated signaling and angiogenesis require Gαi1 and Gαi3.International journal of biological sciences · 2023
    Article
  7. Article
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  9. Review
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  14. Immune checkpoints and cancer in the immunogenomics era.Briefings in functional genomics · 2019
    Review
  15. Article
  16. Article
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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

10 authors at 8 institutions in 2 countries.

Zhanwei Wang
Rica Dela Cruz
Fang Ji
Sheng Guo
Jianhua Zhang
Ying Wang
Gen-Sheng Feng
Lutz Birnbaumer
Meisheng JiangCancer Biology Program, University of Hawaii Cancer Center, 701 Ilalo Street, Honolulu, HI 96813, USA. jm@ucla.edu.
Wen-Ming Chu
University of California, Los Angeles · USUniversity of Hawaiʻi at Mānoa · USCancer Center of Hawaii · USNational Institutes of Health · USRenji Hospital · CNShanghai Jiao Tong University · CNUniversity of California, San Diego · USUniversity of Hawaii Cancer Center

Funding

University of Hawaii Cancer Center CCSGP30CA071789 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI Xin Chen · 1996 to 2026
$56.2M
Transmembrane Signaling MechanismsZIAES101643 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI BIRNBAUMER, LUTZ · 2011 to 2014
$5.4M
Mechansim of activation of innate immunity by ISS-DNAR01AI054128 · NIAID · UNIVERSITY OF HAWAII AT MANOA · PI CHU, WEN-MING · 2002 to 2013
$2.7M
Modulation of Insulin Secretion via Go2 G-ProteinR01DK069771 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JIANG, MEISHENG · 2005 to 2009
$1.6M
Intramural NIH HHSNIAID NIH HHS AI054128NIDDK NIH HHS DK069771PHS HHS 201-101643
6 · The paper itself

Abstract

backgroundIn a classic model, G(i)α proteins including G(i1)α, G(i2)α and G(i3)α are important for transducing signals from G(i)α protein-coupled receptors (G(i)αPCRs) to their downstream cascades in response to hormones and neurotransmitters. Our previous study has suggested that G(i1)α, G(i2)α and G(i3)α are also important for the activation of the PI3K/Akt/mTORC1 pathway by epidermal growth factor (EGF) and its family members. However, a genetic role of these G(i)α proteins in the activation of extracellular signal-regulated protein kinase 1 and 2 (ERK1/2) by EGF is largely unknown. Further, it is not clear whether these G(i)α proteins are also engaged in the activation of both the Akt/mTORC1 and ERK1/2 pathways by other growth factor family members. Additionally, a role of these G(i)α proteins in breast cancer remains to be elucidated.

resultsWe found that Gi1/3 deficient MEFs with the low expression level of G(i2)α showed defective ERK1/2 activation by EGFs, IGF-1 and insulin, and Akt and mTORC1 activation by EGFs and FGFs. Gi1/2/3 knockdown breast cancer cells exhibited a similar defect in the activations and a defect in in vitro growth and invasion. The G(i)α proteins associated with RTKs, Gab1, FRS2 and Shp2 in breast cancer cells and their ablation impaired Gab1's interactions with Shp2 in response to EGF and IGF-1, or with FRS2 and Grb2 in response to bFGF.

conclusionsG(i)α proteins differentially regulate the activation of Akt, mTORC1 and ERK1/2 by different families of growth factors. G(i)α proteins are important for breast cancer cell growth and invasion.

Indexed as

MAP Kinase Signaling SystemAdaptor Proteins, Signal TransducingAnimalsBreast NeoplasmsCell Line, TumorCell ProliferationFibroblast Growth FactorsGTP-Binding Protein alpha Subunits, Gi-GoHumansInsulin-Like Growth Factor IMechanistic Target of Rapamycin Complex 1MiceMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Multiprotein ComplexesProto-Oncogene Proteins c-aktAdaptor Proteins, Signal TransducingFibroblast Growth FactorsGTP-Binding Protein alpha Subunits, Gi-GoInsulin-Like Growth Factor IMechanistic Target of Rapamycin Complex 1Mitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Multiprotein ComplexesProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases

Identifiers

PMID24521094
PMCPMC3937014
OpenAlexW2133679103

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.