Evidence map›Paper›PMID 23111735›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2012

A proteomic study of potential VEGF-C-associated proteins in bladder cancer T24 cells.

Hui-hui Zhang, Fan Qi, Xiong-bing Zu, You-han Cao, Jian-guang Miao, Liang Xu, Lin Qi

Abstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Blockade of MMP-2 and MMP-9 inhibits corneal lymphangiogenesis.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2017
    Article
  6. Silencing of HMGA2 suppresses cellular proliferation, migration, invasion, and epithelial-mesenchymal transition in bladder cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  7. Article
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 4 institutions in 1 country.

Hui-hui ZhangDepartment of Urology, First Affiliated Hospital of Nanhua University, Hengyang city, China.
Fan Qi
Xiong-bing Zu
You-han Cao
Jian-guang Miao
Liang Xu
Lin Qi
Central South University · CNFirst Affiliated Hospital of University of South China · CNUniversity of South China · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOverexpression of vascular endothelial growth factor-C (VEGF-C) has been found to play an important role in malignant progression of various cancer cells, in addition to lymphangiogenesis. However, the mechanisms involved are still largely unknown. Our early research has confirmed that the expression of VEGF-C in bladder cancer was markedly higher than that in normal bladder tissues. VEGF-C can also obviously promote proliferation and invasion of bladder cancer T24 cells. In the present work, we attempted to use proteomic analysis to screen out potential VEGF-C-associated proteins involved in malignant progression of the bladder cancer T24 cells. MATERIAL/

methodsLentivirus vector-based RNA interference (RNAi) was employed to diminish VEGF-C expression of bladder cancer T24 cells. Then we performed comparative proteome analysis to explore differentially expressed proteins in T24 cells with and without VEGF-C siRNA, by two-dimensional difference gel electrophoresis (2D-DIGE).

resultsTwenty-three proteins were identified. Some proteins (matrix metalloproteinase-9, Keratin 8, Serpin B5, Annexin A8) with significant differences were further confirmed by Western blotting.

conclusionsThe 23 potential VEGF-C-associated proteins identified in our study provide us with further insights into the mechanism of VEGF-C promoting malignant progression of bladder cancer cells.

Indexed as

Blotting, WesternCell Line, TumorHumansMatrix Metalloproteinase 9Neoplasm InvasivenessNeoplasm ProteinsProteomicsReproducibility of ResultsRNA, Small InterferingSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTwo-Dimensional Difference Gel ElectrophoresisUrinary Bladder NeoplasmsVascular Endothelial Growth Factor CMatrix Metalloproteinase 9Neoplasm ProteinsRNA, Small InterferingVascular Endothelial Growth Factor CVEGFC protein, human

Identifiers

PMID23111735
PMCPMC3560612
OpenAlexW2168242356

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.