Evidence map›Paper›PMID 27679857›Full record

ReviewThe Biochemical journal2016

Molecular signaling cascades involved in nonmelanoma skin carcinogenesis.

Robert P Feehan, Lisa M Shantz

Open access · greenAbstract readReview
In one paragraph

Review in The Biochemical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  9. Review
  10. A Comprehensive Review of Stem Cell Conditioned Media Role for Anti-Aging on Skin.Stem cells and cloning : advances and applications · 2024
    Review
  11. 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

2 authors at 1 institution in 1 country.

Robert P FeehanDepartment of Cellular and Molecular Physiology, The Pennsylvania State University College of Medicine, 500 University Drive, H166, Hershey, PA 17033, USA.
Lisa M ShantzDepartment of Cellular and Molecular Physiology, The Pennsylvania State University College of Medicine, 500 University Drive, H166, Hershey, PA 17033, USA.
Pennsylvania State University · US

Funding

mTOR-dependent pathways in skin carcinogenesisR21ES019242 · NIEHS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SHANTZ, LISA M · 2010 to 2011
$420k
Evaluation of mTOR as a chemoprevention target in skin cancerR03CA133945 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SHANTZ, LISA M · 2008 to 2009
$154k
Studies of mTORC2 signaling in non-melanoma skin cancerF31ES026471 · NIEHS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI FEEHAN, ROBERT P · 2016 to 2018
$74k
NCI NIH HHS R03 CA133945NIEHS NIH HHS F31 ES026471NIEHS NIH HHS R21 ES019242
6 · The paper itself

Abstract

Nonmelanoma skin cancer (NMSC) is the most common cancer worldwide and the incidence continues to rise, in part due to increasing numbers in high-risk groups such as organ transplant recipients and those taking photosensitizing medications. The most significant risk factor for NMSC is ultraviolet radiation (UVR) from sunlight, specifically UVB, which is the leading cause of DNA damage, photoaging, and malignant transformation in the skin. Activation of apoptosis following UVR exposure allows the elimination of irreversibly damaged cells that may harbor oncogenic mutations. However, UVR also activates signaling cascades that promote the survival of these potentially cancerous cells, resulting in tumor initiation. Thus, the UVR-induced stress response in the skin is multifaceted and requires coordinated activation of numerous pathways controlling DNA damage repair, inflammation, and kinase-mediated signal transduction that lead to either cell survival or cell death. This review focuses on the central signaling mechanisms that respond to UVR and the subsequent cellular changes. Given the prevalence of NMSC and the resulting health care burden, many of these pathways provide promising targets for continued study aimed at both chemoprevention and chemotherapy.

Indexed as

Signal TransductionApoptosisDNA DamageEnzyme ActivationHumansInflammationNeoplasms, Radiation-InducedNF-kappa BOxidative Stressp38 Mitogen-Activated Protein KinasesSkin NeoplasmsSTAT3 Transcription FactorUltraviolet RaysNF-kappa Bp38 Mitogen-Activated Protein KinasesSTAT3 protein, humanSTAT3 Transcription FactorapoptosisDNA damage responsenonmelanoma skin cancersignal transductionultraviolet radiation.

Identifiers

PMID27679857
PMCPMC5198714
OpenAlexW2525263787

What OpenQuestion holds

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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.