Evidence map›Paper›PMID 31109130›Full record

ArticleMolecules (Basel, Switzerland)2019

Norcantharidin Suppresses YD-15 Cell Invasion Through Inhibition of FAK/Paxillin and F-Actin Reorganization.

Kyoung-Ok Hong, Chi-Hyun Ahn, In-Hyoung Yang, Jung-Min Han, Ji-Ae Shin, Sung-Dae Cho, Seong Doo Hong

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Scinderin promotes glioma cell migration and invasionWorld journal of clinical oncology · 2024
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. 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

7 authors at 1 institution in 1 country.

Kyoung-Ok HongDepartment of Oral Pathology, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 03080, Korea. hongko95@snu.sc.kr.
Chi-Hyun AhnDepartment of Oral Pathology, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 03080, Korea. chihyun610@snu.ac.kr.
In-Hyoung YangDepartment of Oral Pathology, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 03080, Korea. inhyoung3@naver.com.
Jung-Min HanDepartment of Oral Pathology, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 03080, Korea. 2017-20655@snu.sc.kr.
Ji-Ae ShinDepartment of Oral Pathology, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 03080, Korea. sky21sm@snu.ac.kr.
Sung-Dae ChoDepartment of Oral Pathology, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 03080, Korea. efiwdsc@snu.ac.kr.ORCID 0000-0001-8670-9579
Seong Doo HongDepartment of Oral Pathology, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 03080, Korea. hongsd@snu.ac.kr.
Seoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Norcantharidin (NCTD), a demethylated derivative of cantharidin, has been reported to exhibit activity against various types of cancers. However, the anti-invasive effects of NCTD and its molecular mechanism in human mucoepidermoid carcinoma (MEC) remain incompletely elucidated. Clonogenic, wound healing, invasion, zymography, western blotting and immunocytochemistry assays were performed in YD-15 cells to investigate the anti-invasive effect of NCTD and its molecular mechanism of action. The inhibitory effects of NCTD on invasiveness were compared with those of a novel focal adhesion kinase (FAK) kinase inhibitor, PF-562271. NCTD markedly suppressed the colony formation, migration, and invasion of YD-15 cells as well as the activities of MMP-2 and MMP-9. It disrupted F-actin reorganization through suppressing the FAK/Paxillin axis. Moreover, NCTD exhibited a powerful anti-invasive effect compared with that of PF-562271 in YD-15 cells. Collectively, these results suggest that NCTD has a potential anti-invasive activity against YD-15 cells. This study may clarify the impact of NCTD on migration and invasion of human MEC cells.

Indexed as

ActinsAntineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicCarcinoma, MucoepidermoidCell Line, TumorCell MovementCell ProliferationCell SurvivalFocal Adhesion Protein-Tyrosine KinasesHumansMatrix Metalloproteinase 2Matrix Metalloproteinase 9Matrix Metalloproteinase InhibitorsPaxillinSignal TransductionActinsAntineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicFocal Adhesion Protein-Tyrosine KinasesMatrix Metalloproteinase 2Matrix Metalloproteinase 9Matrix Metalloproteinase InhibitorsnorcantharidinPaxillinF-actin reorganizationfocal adhesion kinaseinvasionmucoepidermoid carcinomanorcantharidinpaxillin

Identifiers

PMID31109130
PMCPMC6572169
OpenAlexW2946732098

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.