Evidence map›Paper›PMID 30410353›Full record

ArticleOncoTargets and therapy2018

Identification of critically carcinogenesis-related genes in basal cell carcinoma.

Jie Dai, Kang Lin, Yan Huang, Yan Lu, Wen-Qi Chen, Xiao-Rong Zhang, Bang-Shun He, Yu-Qin Pan, Shu-Kui Wang, Wei-Xin Fan

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

  1. Imaging transcriptomics in basal cell carcinoma: Coupling in vivo tumor morphology with gene expression.JID innovations : skin science from molecules to population health · 2026
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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

10 authors at 1 institution in 1 country.

Jie DaiDepartment of Dermatology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Kang LinDepartment of Laboratory Medicine, Nanjing First Hospital, Nanjing Medical University, Nanjing, China, sk_wang@njmu.edu.cn.
Yan HuangDepartment of Ultrasound, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Yan LuDepartment of Dermatology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China, 13327805737@189.cn.
Wen-Qi ChenDepartment of Dermatology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Xiao-Rong ZhangDepartment of Dermatology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Bang-Shun HeGeneral Clinical Research Center, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Yu-Qin PanGeneral Clinical Research Center, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Shu-Kui WangDepartment of Laboratory Medicine, Nanjing First Hospital, Nanjing Medical University, Nanjing, China, sk_wang@njmu.edu.cn.
Wei-Xin FanDepartment of Dermatology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China, 13327805737@189.cn.
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBasal cell carcinoma (BCC) is a frequent malignant tumor of skin cancers with high morbidity. The objective of this study was to identify critical genes and pathways related to the carcinogenesis of BCC and gain more insights into the underlying molecular mechanisms of BCC. MATERIALS AND

methodsThe gene expression profiles of GSE7553 and GSE103439 were downloaded from the Gene Expression Omnibus database with 19 tumors and 6 normal skin tissues. Differentially expressed genes (DEGs) were screened between BCC samples and normal tissues, followed by gene ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis. Subsequently, protein-protein interaction (PPI) network was constructed for these DEGs, and module analysis was performed.

resultsA total of 313 DEGs were obtained. Among them, 222 genes were upregulated and 91 genes were downregulated. Enrichment analysis indicated that the upregulated genes were significantly enriched in cell cycle and mitosis, while the downregulated genes were mainly associated with unsaturated fatty acid metabolic process and cell differentiation. In addition,

conclusionsThe novel critical DEGs and pathways identified in this study may serve pivotal roles in the carcinogenesis of BCC and indicate more molecular targets for the treatment of BCC.

Indexed as

basal cell carcinomabioinformatics analysisdifferentially expressed genesenrichment analysis

Identifiers

PMID30410353
PMCPMC6199216
OpenAlexW2896850685

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.