Evidence map›Paper›PMID 28574612›Full record

ReviewMolecular carcinogenesis2017

Basal cell carcinoma pathogenesis and therapy involving hedgehog signaling and beyond.

Anshika Bakshi, Sandeep C Chaudhary, Mehtab Rana, Craig A Elmets, Mohammad Athar

Open access · greenAbstract readReview
In one paragraph

Review in Molecular carcinogenesis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 5% 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

67 citing papers in PubMed, 1 synthesis or guideline pooled it, 109 citations in OpenAlex.

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7 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

5 authors at 2 institutions in 1 country.

Anshika BakshiDepartment of Dermatology and Skin Diseases Research Center, University of Alabama at Birmingham, Birmingham, Alabama.
Sandeep C ChaudharyDepartment of Dermatology and Skin Diseases Research Center, University of Alabama at Birmingham, Birmingham, Alabama.
Mehtab RanaDepartment of Dermatology and Skin Diseases Research Center, University of Alabama at Birmingham, Birmingham, Alabama.
Craig A ElmetsDepartment of Dermatology and Skin Diseases Research Center, University of Alabama at Birmingham, Birmingham, Alabama.
Mohammad AtharDepartment of Dermatology and Skin Diseases Research Center, University of Alabama at Birmingham, Birmingham, Alabama.ORCID http://orcid.org/0000-0002-4728-2530
University of Alabama at Birmingham · USRutgers, The State University of New Jersey · US

Funding

Topical Chemoprevention of Skin Cancer BiomarkersR01CA193885 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ELMETS, CRAIG A · 2016 to 2022
$1.7M
Chemoprevention of environmental UVB-induced skin cancer in immunosuppressed miceR01ES026219 · NIEHS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ATHAR, MOHAMMAD · 2016 to 2020
$1.7M
Inhibiting Multiple Molecular Targets for Preventing Non-Melanoma Skin CancerR01CA138998 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ATHAR, MOHAMMAD · 2011 to 2015
$1.5M
Host Defense Mechanisms in Melanoma PathogenesisI01BX003395 · VA · BIRMINGHAM VA MEDICAL CENTER · PI ELMETS, CRAIG A · 2016 to 2019
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BLRD VA I01 BX003395NCI NIH HHS R01 CA138998NCI NIH HHS R01 CA193885NIEHS NIH HHS R01 ES026219
6 · The paper itself

Abstract

Basal cell carcinoma (BCC) of the skin is driven by aberrant hedgehog signaling. Thus blocking this signaling pathway by small molecules such as vismodegib inhibits tumor growth. Primary cilium in the epidermal cells plays an integral role in the processing of hedgehog signaling-related proteins. Recent genomic studies point to the involvement of additional genetic mutations that might be associated with the development of BCCs, suggesting significance of other signaling pathways, such as WNT, NOTCH, mTOR, and Hippo, aside from hedgehog in the pathogenesis of this human neoplasm. Some of these pathways could be regulated by noncoding microRNA. Altered microRNA expression profile is recognized with the progression of these lesions. Stopping treatment with Smoothened (SMO) inhibitors often leads to tumor reoccurrence in the patients with basal cell nevus syndrome, who develop 10-100 of BCCs. In addition, the initial effectiveness of these SMO inhibitors is impaired due to the onset of mutations in the drug-binding domain of SMO. These data point to a need to develop strategies to overcome tumor recurrence and resistance and to enhance efficacy by developing novel single agent-based or multiple agents-based combinatorial approaches. Immunotherapy and photodynamic therapy could be additional successful approaches particularly if developed in combination with chemotherapy for inoperable and metastatic BCCs.

Indexed as

Basal Cell CarcinomaCiliaDisease ProgressionHedgehog ProteinsHumansModels, GeneticMutationSignal TransductionSkin NeoplasmsHedgehog ProteinsBCChedgehogphotodynamic immunotherapytherapeutics

Identifiers

PMID28574612
PMCPMC5962346
OpenAlexW2620716110

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.