Evidence map›Paper›PMID 26175937›Full record

ArticleAmerican journal of cancer research2015

Snail interacts with Id2 in the regulation of TNF-α-induced cancer cell invasion and migration in OSCC.

Jing-Ping Zhou, Zhen-Lin Gao, Mei-Ling Zhou, Meng-Ying He, Xiao-Hui Xu, De-Tao Tao, Cong-Chong Yang, Lai-Kui Liu

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Jing-Ping ZhouDepartment of Oral Medicine, School of Stomatology, Wannan Medical College Wuhu, People's Republic of China.
Zhen-Lin GaoDepartment of Oncology IV, First Hospital of Shijiazhuang Shijiazhuang, People's Republic of China.
Mei-Ling ZhouJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University Nanjing, People's Republic of China ; Department of Basic Science of Stomatology, Affiliated Hospital of Stomatology, Nanjing Medical University Nanjing, People's Republic of China.
Meng-Ying HeJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University Nanjing, People's Republic of China ; Department of Basic Science of Stomatology, Affiliated Hospital of Stomatology, Nanjing Medical University Nanjing, People's Republic of China.
Xiao-Hui XuJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University Nanjing, People's Republic of China ; Department of The First Outpatient, Affiliated Hospital of Stomatology, Nanjing Medical University Nanjing, People's Republic of China.
De-Tao TaoDepartment of Oral and Maxillofacial Surgery, The First Affiliated Hospital of Wannan Medical College Wuhu, People's Republic of China.
Cong-Chong YangJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University Nanjing, People's Republic of China ; Department of Basic Science of Stomatology, Affiliated Hospital of Stomatology, Nanjing Medical University Nanjing, People's Republic of China.
Lai-Kui LiuJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University Nanjing, People's Republic of China ; Department of Basic Science of Stomatology, Affiliated Hospital of Stomatology, Nanjing Medical University Nanjing, People's Republic of China.
Nanjing Medical University · CNWannan Medical College · CNFirst Hospital of Shijiazhuang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The inflammatory tumor microenvironment has been identified to play a pivotal role in tumor development and metastasis. Tumor necrosis factor-α (TNF-α) is one of the key cytokines that regulate the inflammatory processes in tumor promotion. In the current study, we treated three oral squamous cell carcinoma (OSCC) cell lines with TNF-α to study its role in inflammation-induced tumor progression. Here we show that TNF-α induces stabilization of the transcriptional repressor Snail and activates NF-κB pathway in the three OSCC cell lines. These activities resulted in the increased motility and invasiveness of three OSCC cell lines. In addition, upon dealing with TNF-α for the indicated time, three OSCC cell lines underwent epithelial-to-mesenchymal transition (EMT), in which they presented a fibroblast-like phenotype and had a decreased expression of epithelial marker (E-cadherin) and an increased expression of mesenchymal marker (vimentin). We further demonstrated that TNF-α can up-regulate the expression of Id2 while inducing an EMT in oral cancer cells. Finally, we showed that Id2 interacted with Snail which may constrain Snail-dependent suppression of E-cadherin. In conclusion, our study indicates that TNF-α induces Snail stabilization is dependent on the activation of NF-κB pathway and results in increasing cell invasion and migration in OSCC cells. Id2 may contribute to regulate the function of Snail during TNF-α-mediated EMT in OSCC. These findings have significant implications for inflammation-induced tumor promotion in OSCC.

Indexed as

Epithelial-to-mesenchymal transitionId2oral squamous cell carcinomaSnailtumor necrosis factor-α

Identifiers

PMID26175937
PMCPMC4497435
OpenAlexW2336506257

What OpenQuestion holds

Textmetadata
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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.