Evidence map›Paper›PMID 29055016›Full record

ArticleCancer research2017

SGK1 Is a Critical Component of an AKT-Independent Pathway Essential for PI3K-Mediated Tumor Development and Maintenance.

Arturo Orlacchio, Michela Ranieri, Martina Brave, Valeria Antico Arciuch, Toni Forde, Daniela De Martino, Karen E Anderson, Phillip Hawkins, Antonio Di Cristofano

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. ROS signaling-induced mitochondrial Sgk1 expression regulates epithelial cell renewal.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Article
  13. Discovery of a novel Aurora B inhibitor GSK650394 with potent anticancer and anti-Journal of enzyme inhibition and medicinal chemistry · 2022
    Article
  14. Article
  15. Article
  16. Article
  17. Convergent genomic and pharmacological evidence of PI3K/GSK3 signaling alterations in neurons from schizophrenia patients.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
  18. Review
  19. Article
  20. Review
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

9 authors at 2 institutions in 2 countries.

Arturo OrlacchioDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Michela RanieriDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Martina BraveDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Valeria Antico ArciuchDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Toni FordeDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Daniela De MartinoDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Karen E AndersonInositide Laboratory, Babraham Institute, Babraham, Cambridge, United Kingdom.
Phillip HawkinsInositide Laboratory, Babraham Institute, Babraham, Cambridge, United Kingdom.
Antonio Di CristofanoDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York. antonio.dicristofano@einstein.yu.edu.
Albert Einstein College of Medicine · USBabraham Institute · GB

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI STEVEN C. ALMO · 1985 to 2026
$111.2M
SPORE in Thyroid CancerP50CA172012 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI FAGIN, JAMES A · 2014 to 2018
$10.3M
Molecular analysis and therapeutic targeting of PI3K signaling in thyroid cancerR01CA128943 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI DI CRISTOFANO, ANTONIO · 2009 to 2024
$5.8M
PI3K-mediated metabolic alterations in the pre-neoplastic thyroidR01CA167839 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI DI CRISTOFANO, ANTONIO · 2013 to 2017
$1.7M
High-speed/resolution whole slide scanner supported by two core facilitiesS10OD019961 · OD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI CONDEELIS, JOHN S · 2015 to 2015
$326k
Biotechnology and Biological Sciences Research Council BBS/E/B/000C0413Biotechnology and Biological Sciences Research Council BBS/E/B/000C0415NCI NIH HHS P30 CA013330NCI NIH HHS P50 CA172012NCI NIH HHS R01 CA128943NCI NIH HHS R01 CA167839NIH HHS S10 OD019961
6 · The paper itself

Abstract

Activation of the PI3K-AKT signaling cascade is a common critical event during malignant transformation. In this study, we used thyroid gland epithelial cells and a series of genetically engineered mouse strains as model systems to demonstrate that, although necessary, AKT activation is not sufficient for PI3K-driven transformation. Instead, transformation requires the activity of the PDK1-regulated AGC family of protein kinases. In particular, SGK1 was found to be essential for proliferation and survival of thyroid cancer cells harboring PI3K-activating mutations. Notably, cotargeting SGK1 and AKT resulted in significantly higher growth suppression than inhibiting either PI3K or AKT alone. Overall, these findings underscore the clinical relevance of AKT-independent pathways in tumors driven by genetic lesions targeting the PI3K cascade.

Indexed as

AnimalsCell Line, TumorCell ProliferationCell SurvivalCell Transformation, NeoplasticHEK293 CellsHumansImmediate-Early ProteinsMiceMice, TransgenicOncogene Protein v-aktPhosphatidylinositol 3-KinasesProtein Serine-Threonine KinasesSerum-Glucocorticoid Regulated KinasesSignal TransductionThyroid NeoplasmsImmediate-Early ProteinsOncogene Protein v-aktPhosphatidylinositol 3-KinasesProtein Serine-Threonine KinasesSerum-Glucocorticoid Regulated Kinases

Identifiers

PMID29055016
PMCPMC5732884
OpenAlexW2765429918

What OpenQuestion holds

Textmetadata
LicenceTDM
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.