Evidence map›Paper›PMID 25051360›Full record

ReviewOncotarget2014

Deregulation of the EGFR/PI3K/PTEN/Akt/mTORC1 pathway in breast cancer: possibilities for therapeutic intervention.

Nicole M Davis, Melissa Sokolosky, Kristin Stadelman, Steve L Abrams, Massimo Libra, Saverio Candido, Ferdinando Nicoletti, Jerry Polesel, Roberta Maestro, Antonino D'Assoro and 16 more

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 135 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
135citing papers in PubMed, 3 pooled it
13.7field-weighted citation impact, top 1% 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

135 citing papers in PubMed, 3 syntheses or guidelines pooled it, 243 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. The cross-talk between GSK-3β, RKIP, and PTEN as potential targets for therapeutic implications in cancer: a comprehensive insight.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2026
    Review
  7. In Silico Analysis of Squamous Cell Carcinoma.Advances in experimental medicine and biology · 2026
    Review
  8. Article
  9. Review
  10. 3‑Phenethyl-2-phenylquinazolin-4(3ACS pharmacology & translational science · 2025
    Article
  11. Article
  12. Review
  13. Article
  14. Role of BRCA1 in glioblastoma etiology.Cellular oncology (Dordrecht, Netherlands) · 2024
    Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. SDC4-rs1981429 and ATM-rs228590 may provide early biomarkers of breast cancer risk.Journal of cancer research and clinical oncology · 2023
    Article

75 more citing papers are in PubMed but not listed here.

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

26 authors at 12 institutions in 6 countries.

Nicole M DavisDepartment of Microbiology and Immunology, Brody School of Medicine at East Carolina University Greenville, NC 27858 USA.
Melissa SokoloskyDepartment of Microbiology and Immunology, Brody School of Medicine at East Carolina University Greenville, NC 27858 USA.
Kristin StadelmanDepartment of Microbiology and Immunology, Brody School of Medicine at East Carolina University Greenville, NC 27858 USA.
Steve L AbramsDepartment of Microbiology and Immunology, Brody School of Medicine at East Carolina University Greenville, NC 27858 USA.
Massimo LibraDepartment of Bio-Medical Sciences, University of Catania, Catania, Italy.
Saverio CandidoDepartment of Bio-Medical Sciences, University of Catania, Catania, Italy.
Ferdinando NicolettiDepartment of Bio-Medical Sciences, University of Catania, Catania, Italy.
Jerry PoleselUnit of Epidemiology and Biostatistics, Centro di Riferimento Oncologico, IRCCS, Aviano, Italy.
Roberta MaestroExperimental Oncology 1, CRO IRCCS, National Cancer Institute, Aviano, Pordenone, Italy.
Antonino D'AssoroDepartment of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Rochester, MN, USA.
Lyudmyla DrobotPalladin Institute of Biochemistry, National Academy of Sciences of Ukraine, Kyiv, Ukraine.
Dariusz RakusDepartment of Animal Molecular Physiology, Institute of Experimental Biology, Wroclaw University, Wroclaw, Poland.
Agnieszka GizakDepartment of Animal Molecular Physiology, Institute of Experimental Biology, Wroclaw University, Wroclaw, Poland.
Piotr LaidlerChair of Medical Biochemistry, Jagiellonian University Medical College, Kraków, Poland.
Joanna Dulińska-LitewkaChair of Medical Biochemistry, Jagiellonian University Medical College, Kraków, Poland.
Joerg BaseckeDepartment of Medicine University of Göttingen, Göttingen, Germany.
Sanja MijatovicDepartment of Immunology, Institute for Biological Research "Sinisa Stankovic" University of Belgrade, Belgrade, Serbia.
Danijela Maksimovic-IvanicDepartment of Immunology, Institute for Biological Research "Sinisa Stankovic" University of Belgrade, Belgrade, Serbia.
Giuseppe MontaltoBiomedical Department of Internal Medicine and Specialties, University of Palermo, Palermo, Italy; Consiglio Nazionale delle Ricerche,Istituto di Biomedicina e Immunologia Molecolare "Alberto Monroy", Palermo, Italy.
Melchiorre CervelloConsiglio Nazionale delle Ricerche,Istituto di Biomedicina e Immunologia Molecolare "Alberto Monroy", Palermo, Italy.
Timothy L FitzgeraldDepartment of Surgery, Brody School of Medicine at East Carolina University, Greenville, NC.
Zoya DemidenkoDepartment of Cell Stress Biology, Roswell Park Cancer Institute, Buffalo, NY, USA.
Alberto M MartelliDipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.
Lucio CoccoDipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.
Linda S SteelmanDepartment of Microbiology and Immunology, Brody School of Medicine at East Carolina University Greenville, NC 27858 USA.
James A McCubreyDepartment of Microbiology and Immunology, Brody School of Medicine at East Carolina University Greenville, NC 27858 USA.
East Carolina University · USUniversity of Catania · ITCentro di Riferimento Oncologico · ITIstituto di Biomedicina e di Immunologia Molecolare Alberto Monroy · ITJagiellonian University · PLUniversity of Belgrade · RSUniversity of Bologna · ITUniversity of Wrocław · PLMayo Clinic · USPalladin Institute of Biochemistry · UARoswell Park Comprehensive Cancer Center · USUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The EGFR/PI3K/PTEN/Akt/mTORC1/GSK-3 pathway plays prominent roles in malignant transformation, prevention of apoptosis, drug resistance and metastasis. The expression of this pathway is frequently altered in breast cancer due to mutations at or aberrant expression of: HER2, ERalpha, BRCA1, BRCA2, EGFR1, PIK3CA, PTEN, TP53, RB as well as other oncogenes and tumor suppressor genes. In some breast cancer cases, mutations at certain components of this pathway (e.g., PIK3CA) are associated with a better prognosis than breast cancers lacking these mutations. The expression of this pathway and upstream HER2 has been associated with breast cancer initiating cells (CICs) and in some cases resistance to treatment. The anti-diabetes drug metformin can suppress the growth of breast CICs and herceptin-resistant HER2+ cells. This review will discuss the importance of the EGFR/PI3K/PTEN/Akt/mTORC1/GSK-3 pathway primarily in breast cancer but will also include relevant examples from other cancer types. The targeting of this pathway will be discussed as well as clinical trials with novel small molecule inhibitors. The targeting of the hormone receptor, HER2 and EGFR1 in breast cancer will be reviewed in association with suppression of the EGFR/PI3K/PTEN/Akt/mTORC1/GSK-3 pathway.

Indexed as

Breast NeoplasmsClass I Phosphatidylinositol 3-KinasesErbB ReceptorsFemaleGene Expression Regulation, NeoplasticHumansMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSignal TransductionTOR Serine-Threonine KinasesClass I Phosphatidylinositol 3-KinasesErbB ReceptorsMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesPhosphatidylinositol 3-KinasesPIK3CA protein, humanProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanTOR Serine-Threonine Kinases

Identifiers

PMID25051360
PMCPMC4148087
OpenAlexW2141202224

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.