Evidence map›Paper›PMID 31370278›Full record

ReviewCells2019

Role and Therapeutic Targeting of the PI3K/Akt/mTOR Signaling Pathway in Skin Cancer: A Review of Current Status and Future Trends on Natural and Synthetic Agents Therapy.

Jean Christopher Chamcheu, Tithi Roy, Mohammad Burhan Uddin, Sergette Banang-Mbeumi, Roxane-Cherille N Chamcheu, Anthony L Walker, Yong-Yu Liu, Shile Huang

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 3 pooled it
9.0field-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

106 citing papers in PubMed, 3 syntheses or guidelines pooled it, 192 citations in OpenAlex.

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  19. Cancer chemoprevention: signaling pathways and strategic approaches.Signal transduction and targeted therapy · 2025
    Review
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46 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

8 authors at 3 institutions in 1 country.

Jean Christopher ChamcheuCollege of Pharmacy, University of Louisiana at Monroe, Monroe, LA 71209-0497, USA. chamcheu@ulm.edu.
Tithi RoyCollege of Pharmacy, University of Louisiana at Monroe, Monroe, LA 71209-0497, USA.
Mohammad Burhan UddinCollege of Pharmacy, University of Louisiana at Monroe, Monroe, LA 71209-0497, USA.
Sergette Banang-MbeumiCollege of Pharmacy, University of Louisiana at Monroe, Monroe, LA 71209-0497, USA.
Roxane-Cherille N ChamcheuCollege of Pharmacy, University of Louisiana at Monroe, Monroe, LA 71209-0497, USA.
Anthony L WalkerCollege of Pharmacy, University of Louisiana at Monroe, Monroe, LA 71209-0497, USA.
Yong-Yu LiuCollege of Pharmacy, University of Louisiana at Monroe, Monroe, LA 71209-0497, USA.
Shile HuangDepartment of Biochemistry and Molecular Biology, Louisiana State University Health Sciences Center, 1501 Kings Highway, Shreveport, LA 71130-3932, USA.
University of Louisiana at Monroe · USDelta Air Lines (United States) · USLouisiana State University Health Sciences Center Shreveport · US

Funding

Skin Diseases Research Center at the University of WisconsinP30AR066524 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI WOOD, GARY S · 2014 to 2018
$2.6M
NIAMS NIH HHS P30 AR066524
6 · The paper itself

Abstract

The mammalian or mechanistic target of rapamycin (mTOR) and associated phosphatidyl-inositiol 3-kinase (PI3K)/protein kinase B (Akt) pathways regulate cell growth, differentiation, migration, and survival, as well as angiogenesis and metabolism. Dysregulation of these pathways is frequently associated with genetic/epigenetic alterations and predicts poor treatment outcomes in a variety of human cancers including cutaneous malignancies like melanoma and non-melanoma skin cancers. Recently, the enhanced understanding of the molecular and genetic basis of skin dysfunction in patients with skin cancers has provided a strong basis for the development of novel therapeutic strategies for these obdurate groups of skin cancers. This review summarizes recent advances in the roles of PI3K/Akt/mTOR and their targets in the development and progression of a broad spectrum of cutaneous cancers and discusses the current progress in preclinical and clinical studies for the development of PI3K/Akt/mTOR targeted therapies with nutraceuticals and synthetic small molecule inhibitors.

Indexed as

AnimalsAntineoplastic AgentsBiological ProductsClinical Trials as TopicHumansMolecular Targeted TherapyPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionSkin NeoplasmsTOR Serine-Threonine KinasesAntineoplastic AgentsBiological ProductsMTOR protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesAktbasal cell carcinomamelanomaMerkel cell carcinomamTORphytochemicalsPI3Kskin cancerssquamous cell carcinomatargeted therapy

Identifiers

PMID31370278
PMCPMC6721560
OpenAlexW2966111877

What Socratic 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 Socratic graph.