Evidence map›Paper›PMID 38548549›Full record

ArticleAnais brasileiros de dermatologia

Expression analysis and biological regulation of silencing regulatory protein 6 (SIRT6) in cutaneous squamous cell carcinoma.

Sai Chen, Hongxia Chen, Xu Wang, Dongmei Zhang, Li Zhang, Jiawei Cheng, Qi Zhang, Zhixiang Hua, Xu Miao, Jian Shi

Open access · goldAbstract read
In one paragraph

Article in Anais brasileiros de dermatologia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 95% 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

2 citing papers in PubMed, 0 citations in OpenAlex.

  1. 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

10 authors at 1 institution in 1 country.

Sai ChenDepartment of Dermatology, Affiliated Hospital 2 of Nantong University, People's Republic of China.
Hongxia ChenDepartment of Dermatology, Affiliated Hospital 2 of Nantong University, People's Republic of China.
Xu WangDepartment of Dermatology, Affiliated Hospital 2 of Nantong University, People's Republic of China.
Dongmei ZhangJiangsu Provincial Medical Key Discipline (Laboratory) Cultivation Unit of Immunology, Nantong First People's Hospital, People's Republic of China; Medical Research Center, Affiliated Hospital 2 of Nantong University, People's Republic of China.
Li ZhangDepartment of Dermatology, Affiliated Hospital 2 of Nantong University, People's Republic of China.
Jiawei ChengDepartment of Dermatology, Affiliated Hospital 2 of Nantong University, People's Republic of China.
Qi ZhangDepartment of Dermatology, Affiliated Hospital 2 of Nantong University, People's Republic of China.
Zhixiang HuaDepartment of Dermatology, Affiliated Hospital 2 of Nantong University, People's Republic of China.
Xu MiaoDepartment of Dermatology, Affiliated Hospital 2 of Nantong University, People's Republic of China.
Jian ShiDepartment of Dermatology, Affiliated Hospital 2 of Nantong University, People's Republic of China. Electronic address: jsntmcsj@163.com.
Nantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCutaneous squamous cell carcinoma (CSCC) is one of the most common types of skin cancer worldwide. Therefore, the identification of biomarkers associated with CSCC progression could aid in the early detection of high-risk squamous cell carcinoma and the development of novel therapeutic strategies.

objectiveThis study aimed to investigate the expression patterns of silent mating type Information Regulation 2 homolog 6 (SIRT6) in CSCC and its clinical significance.

methodsThe protein expression level of SIRT6 in tissues was detected by immunohistochemistry, and the correlation between SIRT6 expression and clinicopathological parameters in CSCC patients was analyzed. The relative expression of SIRT6 in CSCC cell lineage and tissue specimens was determined by western blotting and PCR. The effect of SIRT6 silencing on cell proliferation was evaluated using cell counting kit 8. Wound healing, transwell method, and flow cytometry were used to investigate the migration, invasion, and cell cycle distribution/apoptosis of CSCC cells after SIRT6 silencing, respectively. Western blot was used to detect the expression of EMT (Epithelial-Mesenchymal Transition), cycle, apoptosis, and other related proteins.

resultsThe high expression of SIRT6 was correlated with the location of cancer tissue and Broder staging in CSCC patients. Knockdown of SIRT6 inhibited the proliferation, migration, invasion and EMT of CSCC cells, and promoted their apoptosis, with cells blocked in G1 phase. STUDY LIMITATIONS: No animal experiments were conducted to further verify the results.

conclusionDecreased expression of SIRT6 can inhibit the occurrence and development of CSCC.

Indexed as

ApoptosisCarcinoma, Squamous CellCell ProliferationSirtuinsSkin NeoplasmsAgedBiomarkers, TumorBlotting, WesternCell CycleCell Line, TumorCell MovementEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansImmunohistochemistryBiomarkers, TumorSIRT6 protein, humanSirtuinsBiomarkersCarcinoma, squamous cellHistologySirtuin-6

Identifiers

PMID38548549
PMCPMC11220918
OpenAlexW4393237042

What Socratic holds

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LicenceCC BY
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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 Socratic graph.