Evidence map›Paper›PMID 32015216›Full record

ArticleAging2020

Abnormal overexpression of G9a in melanoma cells promotes cancer progression via upregulation of the Notch1 signaling pathway.

Ning-Ning Dang, Jing Jiao, Xianguang Meng, Yunhe An, Chen Han, Shuhong Huang

Open access · greenAbstract read
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

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  11. Impact ofInternational journal of molecular medicine · 2022
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  14. Epigenetics in the Diagnosis and Therapy of Malignant Melanoma.International journal of molecular sciences · 2022
    Review
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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

6 authors at 3 institutions in 1 country.

Ning-Ning DangDepartment of Dermatology, Jinan Central Hospital Affiliated to Shandong University, Jinan, Shandong Province, China.
Jing JiaoDepartment of Dermatology, Jinan Central Hospital Affiliated to Shandong University, Jinan, Shandong Province, China.
Xianguang MengDepartment of Dermatology, Jinan Central Hospital Affiliated to Shandong University, Jinan, Shandong Province, China.
Yunhe AnBeijing Center for Physical and Chemical Analysis, Beijing, China.
Chen HanInstitute of Basic Medicine, The First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong Province, China.
Shuhong HuangInstitute of Basic Medicine, The First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong Province, China.
Jinan Central Hospital · CNShandong First Medical University · CNBeijing Academy of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant melanoma is a type of very dangerous skin cancer. Histone modifiers usually become dysregulated during the process of carcinoma development, thus there is potential for a histone modifier inhibitor as a useful drug for cancer therapy. There is a multitude of evidence regarding the role of G9a, a histone methyltransferase (HMTase), in tumorigenesis. In this study, we first showed that G9a was significantly upregulated in melanoma patients. Using the TCGA database, we found a significantly higher expression of G9a in primary melanoma samples (n = 461) compared to normal skin samples (n = 551). Next, we knocked down G9a in human M14 and A375 melanoma cell lines

Indexed as

AnimalsBiomarkers, TumorCutaneous Malignant MelanomaDisease ProgressionFemaleHeterograftsHistocompatibility AntigensHistone-Lysine N-MethyltransferaseHumansMaleMelanomaMiceReceptor, Notch1Signal TransductionSkin NeoplasmsUp-RegulationBiomarkers, TumorEHMT2 protein, humanHistocompatibility AntigensHistone-Lysine N-MethyltransferaseNOTCH1 protein, humanReceptor, Notch1G9amelanomaNotch1proliferationUNC0642

Identifiers

PMID32015216
PMCPMC7041736
OpenAlexW3004491023

What OpenQuestion 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 OpenQuestion graph.