Evidence map›Paper›PMID 22484636›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2012

Increased expression of PRL-1 protein correlates with shortened patient survival in human hepatocellular carcinoma.

J-W Lu, J-G Chang, K-T Yeh, R-M Chen, J J P Tsai, W-W Su, R-M Hu

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Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 29% of its field
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

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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Overexpression of PTP4A1 is associated with poor overall survival in non-small cell lung cancer.International journal of clinical and experimental pathology · 2018
    Article
  7. Article
  8. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

J-W LuDepartment of Biotechnology, Asia University, Wufeng, Taichung, Taiwan.
J-G Chang
K-T Yeh
R-M Chen
J J P Tsai
W-W Su
R-M Hu
Asia University · TWChanghua Christian Hospital · TWKaohsiung Medical University · TWNational University of Tainan · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe purposes of the current study were to investigate whether overexpression of the PRL-1 is clinically relevant to hepatocellular carcinoma (HCC) and whether expression patterns of PRL-1 in HCC have diagnostic and prognostic value.

methodsImmunohistochemistry analysis was performed for PRL-1 in 60 HCC samples. The data were correlated with clinicopathological features. The univariate and multivariate survival analyses were also performed to determine their prognostic significance.

resultsPRL-1 protein was overexpressed (83%) in HCC as compared with the adjacent normal tissue. PRL-1 expression was not influenced by chronic alcohol exposure or cirrhosis. High expression of PRL-1 was correlated with smoking (p=0.012), cirrhosis (p=0.047) and histological grade (p=0.055). The Kaplan-Meier survival curves showed that high PRL-1 expression related to a poor survival with statistical significance (I vs. III, p=0.010; II vs. III, p=0.001). Univariate analysis showed that PRL-1 expression was associated with tumour size, stage and PRL-1 score. Multivariate analysis revealed that the PRL-1 protein expression level was an independent factor for overall survival (HR, 5.367; 95% CI, 2.270-12.692; p=0.001). This is the first demonstration that the expression level of PRL-1 is correlated with tumour progression and prognosis in HCC.

conclusionsAlong with other results, the PRL-1 protein is a candidate biomarker and a potential target for novel therapies against human HCC progression.

Indexed as

Gene Expression Regulation, NeoplasticAdolescentAdultAgedBiomarkersCarcinoma, HepatocellularCell Cycle ProteinsDisease ProgressionFemaleGene Expression ProfilingHumansImmunohistochemistryLiverLiver NeoplasmsMaleMembrane ProteinsBiomarkersCell Cycle ProteinsMembrane ProteinsProtein Tyrosine PhosphatasesPTP4A1 protein, human

Identifiers

PMID22484636
OpenAlexW2031063309

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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.