Evidence map›Paper›PMID 26722601›Full record

ArticleInternational journal of clinical and experimental pathology2015

CISD2 associated with proliferation indicates negative prognosis in patients with hepatocellular carcinoma.

Bin Chen, Shunli Shen, Jian Wu, Yunpeng Hua, Ming Kuang, Shaoqiang Li, Baogang Peng

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 21% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  10. An Examination ofEvidence-based complementary and alternative medicine : eCAM · 2021
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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.

Bin ChenDepartment of Hepatic Surgery, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Shunli ShenDepartment of Hepatic Surgery, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Jian WuDepartment of Hepatic Surgery, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Yunpeng HuaDepartment of Hepatic Surgery, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Ming KuangDepartment of Hepatic Surgery, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Shaoqiang LiDepartment of Hepatic Surgery, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Baogang PengDepartment of Hepatic Surgery, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAn evolutionarily conserved gene, the CDGSH iron sulfur domain 2 (CISD2), functions to control mammalian life span and regulates human cells proliferation. However, the role of CISD2 in HCC remains unclear. This study was aimed at investigating the expression pattern and clinicopathological significance of CISD2 in patients with HCC.

methodsThe mRNA and protein expression levels of CISD2 were analyzed in six HCC lines and eight paired hepatic cancer tumors by real-time PCR, Western blotting and immunohistochemical staining. Statistical analysis was used to evaluate the clinicopathological significance of CISD2 expression. Short hairpin RNA interfering approach was employed to suppress endogenous CISD2 expression in hepatic cancer cells to determine its role in proliferation.

resultsCISD2 expression in liver cancer cell lines and tissues was significantly up-regulated at both the RNA and protein levels compared with that in normal cells and adjacent non-tumorous liver tissues (ANT). CISD2 was an independent prognostic factor for poor prognosis. It was correlated with tumor size (P=0.001), number of tumors (P=0.003), surgical margin (P=0.006), hepatitis B surface antigen (HBsAg) infection (P=0.002) and recurrence (P<0.001) of liver cancer. Multivariate analysis suggested that CISD2 expression was an independent prognostic indicator for the survival of patients with HCC. HCC patients with high CISD2 expression displayed a shorter overall survival and a higher recurrence rate than those with low CISD2 expression (P<0.05, respectively). Additionally, stable down-expression of CISD2 in hepatoma cells suppressed cell proliferation in vitro. Similarly, an in vivo assay showed that CISD2 down-regulation in hepatoma cells inhibited remarkably tumorigenic potential in tumor size and weight.

conclusionsCISD2 protein may serve as a candidate prognostic marker and a novel therapeutic target for HCC and play an important role in promoting proliferation and enhanced progression of HCC.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAnimalsBiomarkers, TumorCarcinoma, HepatocellularCell ProliferationDisease ProgressionDown-RegulationFemaleHumansLiver NeoplasmsMaleMembrane ProteinsMiddle AgedPrognosisBiomarkers, TumorCISD2 protein, humanMembrane ProteinsCDGSH iron sulfur domain 2hepatocellular carcinomaprognostic markerproliferationtherapeutic target

Identifiers

PMID26722601
PMCPMC4680546
OpenAlexW2222197267

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.