Evidence map›Paper›PMID 26655729›Full record

ArticleScientific reports2015

Combination of NTP with cetuximab inhibited invasion/migration of cetuximab-resistant OSCC cells: Involvement of NF-κB signaling.

Jae Won Chang, Sung Un Kang, Yoo Seob Shin, Seong Jin Seo, Yeon Soo Kim, Sang Sik Yang, Jong-Soo Lee, Eunpyo Moon, Keunho Lee, Chul-Ho Kim

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 43 citations in OpenAlex.

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  19. ROS from Physical Plasmas: Redox Chemistry for Biomedical Therapy.Oxidative medicine and cellular longevity · 2019
    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

10 authors at 2 institutions in 1 country.

Jae Won ChangDepartment of Otolaryngology-Head and Neck Surgery, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Sung Un KangDepartment of Otolaryngology, School of Medicine, Ajou University, Suwon, Republic of Korea.
Yoo Seob ShinDepartment of Otolaryngology, School of Medicine, Ajou University, Suwon, Republic of Korea.
Seong Jin SeoDepartment of Otolaryngology, School of Medicine, Ajou University, Suwon, Republic of Korea.
Yeon Soo KimDepartment of Otolaryngology, School of Medicine, Ajou University, Suwon, Republic of Korea.
Sang Sik YangDepartment of Electrical and Computer Engineering, Ajou University, Suwon, Republic of Korea.
Jong-Soo LeeDepartment of Molecular Science and Technology and Department of Life Science, Ajou University, Suwon, Republic of Korea.
Eunpyo MoonDepartment of Molecular Science and Technology and Department of Life Science, Ajou University, Suwon, Republic of Korea.
Keunho LeePSM America Inc., Colorado Springs, CO, USA.
Chul-Ho KimDepartment of Otolaryngology, School of Medicine, Ajou University, Suwon, Republic of Korea.
Ajou University · KRChungnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the epidermal growth factor receptor (EGFR) is an established target in head-and-neck cancer (HNC), resistance to EGFR-targeted therapy mediated by various mechanisms has been reported. Therefore, a combination strategy to overcome resistance to EGFR mono-targeted therapy is clinically required. We have previously demonstrated that non-thermal atmospheric pressure plasma (NTP) induces death of various cancer cells, including oral squamous cancer (OSCC) cells. In this study, we report for the first time that combining NTP treatment with cetuximab led to inhibition of migration and invasion in cetuximab-resistant OSCC cells, which could be a promising strategy to overcome resistance to anti-EGFR therapy. NTP induced deactivation of NF-κB in SCCQLL1 cells, but not in MSKQLL1 cells. In addition, NTP increased the expression level of E-cadherin, and decreased those of vimentin, Slug, Snail, matrix metalloproteinase (MMP)-2, -9, and activities of MMPs. Moreover, NF-κB upregulation using cDNA diminished the combination effect of NTP on invasion, migration and related signals. Taken together, these results indicate that the combination of NTP with cetuximab can decrease invasiveness in cetuximab-resistant OSCCs through a novel mechanism involving the NF-κB pathway. These findings show the therapeutic potential of treatment that combines NTP and cetuximab in OSCC.

Indexed as

ApoptosisCarcinoma, Squamous CellCell Line, TumorCell MovementCell ProliferationCetuximabDrug Resistance, NeoplasmDrug SynergismEpithelial-Mesenchymal TransitionErbB ReceptorsHumansMatrix Metalloproteinase 2Matrix Metalloproteinase 9Mouth NeoplasmsNF-kappa BPlasma GasesCetuximabErbB ReceptorsMatrix Metalloproteinase 2Matrix Metalloproteinase 9NF-kappa BPlasma GasesTumor Suppressor Protein p53

Identifiers

PMID26655729
PMCPMC4677387
OpenAlexW2400972105

What OpenQuestion holds

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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.