Evidence map›Paper›PMID 23511560›Full record

ArticleBritish journal of cancer2013

Protumoral roles of melanoma inhibitory activity 2 in oral squamous cell carcinoma.

M Kurihara, T Kirita, T Sasahira, H Ohmori, S Matsushima, K Yamamoto, A K Bosserhoff, H Kuniyasu

Open access · bronzeAbstract read
In one paragraph

Article in British journal of cancer, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. The Multifarious Functions of Pyruvate Kinase M2 in Oral Cancer Cells.International journal of molecular sciences · 2018
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. NEDD 4 binding protein 2-like 1 promotes cancer cell invasion in oral squamous cell carcinoma.Virchows Archiv : an international journal of pathology · 2016
    Article
  14. Article
  15. Article
  16. Article
  17. Mechanisms for exporting large-sized cargoes from the endoplasmic reticulum.Cellular and molecular life sciences : CMLS · 2015
    Review
  18. Update of molecular pathobiology in oral cancer: a review.International journal of clinical oncology · 2014
    Review
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 2 institutions in 2 countries.

M KuriharaDepartment of Molecular Pathology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara 634-8521, Japan.
T Kirita
T Sasahira
H Ohmori
S Matsushima
K Yamamoto
A K Bosserhoff
H Kuniyasu
Nara Medical University · JPUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of melanoma inhibitory activity 2 (MIA2) was examined in human oral squamous cell carcinoma (OSCC).

methodsMIA2 role was examined by immunohistochemistry of human OSCCs and knockdown studies using human 3 OSCC cell lines with MIA2 expression.

resultsMIA2 expression was observed in 62 (66.7%) of 93 OSCCs and was associated with tumour expansion and nodal metastasis. Melanoma inhibitory activity 2 expression was inversely correlated with intratumoral infiltration of lymphocytes. Invasion and anti-apoptotic survival were reduced by MIA2 knockdown in HSC3 cells. MOLT-3 lymphocytes infiltrating the HSC3 cell layer was enhanced by MIA2 knockdown or MIA2 depletion with the antibody. In HSC3 cells, MIA2 knockdown decreased the expressions of vascular endothelial growth factor (VEGF), VEGF-C, and VEGF-D. The downregulation of VEGF-C and -D was caused by inhibition of p38 and extracellular signal-regulated kinase (ERK)1/2, respectively. Melanoma inhibitory activity 2 was co-precipitated with integrin α4 andα5 in HSC3 cells. Integrin α4 knockdown decreased p38 phosphorylation and increased apoptosis, whereas integrin α5 knockdown decreased c-Jun N-terminal kinase (JNK) phosphorylation and apoptosis. Inhibition of JNK decreased apoptosis in the HSC3 cells.

conclusionThese findings suggest that the roles of MIA2 might be based on the variety of the integrins and the subtypes of mitogen-activated protein kinase.

Indexed as

AgedAntigens, NeoplasmCarcinoma, Squamous CellCell Line, TumorFemaleGene Knockdown TechniquesHumansImmunohistochemistryIntegrinsLymphocytes, Tumor-InfiltratingMaleMiddle AgedMitogen-Activated Protein KinasesMouth NeoplasmsNeoplasm ProteinsTumor Suppressor ProteinsAntigens, NeoplasmIntegrinsMIA2 protein, humanMitogen-Activated Protein KinasesNeoplasm ProteinsTumor Suppressor ProteinsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor CVascular Endothelial Growth Factor DVEGFA protein, humanVEGFC protein, humanVEGFD protein, human

Identifiers

PMID23511560
PMCPMC3629429
OpenAlexW2047955980

What OpenQuestion holds

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Registered trials

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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.