Evidence map›Paper›PMID 28236975›Full record

ReviewCurrent topics in developmental biology2017

SGK1: The Dark Side of PI3K Signaling.

Antonio Di Cristofano

Open access · greenAbstract readReview
In one paragraph

Review in Current topics in developmental biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
9.1field-weighted citation impact, top 2% 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

60 citing papers in PubMed, 99 citations in OpenAlex.

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  20. 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
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

1 author at 1 institution in 1 country.

Antonio Di CristofanoAlbert Einstein College of Medicine, Bronx, NY, United States. Electronic address: antonio.dicristofano@einstein.yu.edu.
Albert Einstein College of Medicine · US

Funding

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
NCI NIH HHS P50 CA172012NCI NIH HHS R01 CA128943NCI NIH HHS R01 CA167839
6 · The paper itself

Abstract

Activation of the PI3K pathway is central to a variety of physiological and pathological processes. In these contexts, AKT is classically considered the de facto mediator of PI3K-dependent signaling. However, in recent years, accumulating data point to the existence of additional effectors of PI3K activity, parallel to and independent of AKT, that play critical and unique roles in mediating different developmental, homeostatic, and pathological processes. In this review, I summarize and discuss our current understanding of the function of the serine/threonine kinase SGK1 as a downstream effector of PI3K, and try to separate targets and pathways validated as uniquely SGK1-dependent from those shared with AKT.

Indexed as

Signal TransductionAnimalsCell DifferentiationEmbryonic DevelopmentEnzyme StabilityHumansImmediate-Early ProteinsNeoplasmsPhosphatidylinositol 3-KinasesProtein Serine-Threonine KinasesSerum-Glucocorticoid Regulated KinasesImmediate-Early ProteinsPhosphatidylinositol 3-KinasesProtein Serine-Threonine KinasesSerum-Glucocorticoid Regulated KinasesAGC kinasesAKTPDK1PI3KSGK1

Identifiers

PMID28236975
PMCPMC5658788
OpenAlexW2566889811

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.