Evidence map›Paper›PMID 23093845›Full record

ArticleJournal of biomedicine & biotechnology2012

Overexpression of runt-related transcription factor-2 is associated with advanced tumor progression and poor prognosis in epithelial ovarian cancer.

Weiping Li, Shujuan Xu, Shuang Lin, Wei Zhao

Abstract read
In one paragraph

Article in Journal of biomedicine & biotechnology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

13 citing papers in PubMed.

  1. Article
  2. Induction of ALP and MMP9 activity facilitates invasive behavior in heterogeneous human BMSC and HNSCC 3D spheroids.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  3. Expression of tissue factor in human cervical carcinoma tissue.Experimental and therapeutic medicine · 2018
    Article
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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

4 authors.

Weiping LiDepartment of Gynaecology and Obstetrics, Clinical Section, PLA General Hospital, Beijing 100853, China.
Shujuan Xu
Shuang Lin
Wei Zhao

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate clinical significance of runt-related transcription factor (RUNX)-2 in epithelial ovarian cancer (EOC).

methodsRUNX2 protein expression and its subcellular localization were detected by immunohistochemistry in 116 patients with EOC.

resultsRUNX2 protein was predominantly expressed in cell nucleus of EOC tissues. The expression level of RUNX2 in EOC tissues was significantly higher than that in normal ovarian tissues (P < 0.001). In addition, the nuclear labeling index (LI) of RUNX2 in tumor cells was significantly associated with the advanced clinical stage of EOC tissues (P = 0.001). Moreover, EOC patients with high RUNX2 LI had significantly shorter overall (P < 0.001) and progression-free (P = 0.002) survival than those with low RUNX2 LI. Especially, subgroup analysis revealed that EOC patients with high clinical stages (III~IV) in high RUNX2 expression group demonstrated a significantly worse clinical outcome than those in low RUNX2 expression group, but patients with low clinical stages (I~II) had no significantly different prognosis between high and low RUNX2 expression groups.

conclusionsOur data suggest for the first time that RUNX2 overexpression is associated with advanced tumor progression and poor clinical outcome of EOC patients. RUNX2 might be a novel prognostic marker of EOC.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCore Binding Factor Alpha 1 SubunitFemaleHumansMiddle AgedNeoplasm ProteinsNeoplasms, Glandular and EpithelialOvarian NeoplasmsPrognosisSubcellular FractionsTissue DistributionUp-RegulationBiomarkers, TumorCore Binding Factor Alpha 1 SubunitNeoplasm ProteinsRUNX2 protein, human

Identifiers

PMID23093845
PMCPMC3475129

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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.