Evidence map›Paper›PMID 26339343›Full record

ArticleInternational journal of clinical and experimental pathology2015

Down-regulation of cancer/testis antigen OY-TES-1 attenuates malignant behaviors of hepatocellular carcinoma cells in vitro.

Jun Fu, Bin Luo, Wen-Wen Guo, Qing-Mei Zhang, Lei Shi, Qi-Ping Hu, Fang Chen, Shao-Wen Xiao, Xiao-Xun Xie

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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

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  9. Opa interacting protein 5 acts as an oncogene in bladder cancer.Journal of cancer research and clinical oncology · 2017
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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

9 authors at 2 institutions in 2 countries.

Jun FuDepartment of Histology & Embryology, School of Pre-clinical Medicine, Guangxi Medical University China.
Bin LuoDepartment of Histology & Embryology, School of Pre-clinical Medicine, Guangxi Medical University China ; Key Laboratory of School of Pre-clinical Medicine, Guangxi Medical University China.
Wen-Wen GuoDepartment of Histology & Embryology, School of Pre-clinical Medicine, Guangxi Medical University China.
Qing-Mei ZhangDepartment of Histology & Embryology, School of Pre-clinical Medicine, Guangxi Medical University China.
Lei ShiDepartment of Histology & Embryology, School of Pre-clinical Medicine, Guangxi Medical University China.
Qi-Ping HuDepartment of Histology & Embryology, School of Pre-clinical Medicine, Guangxi Medical University China.
Fang ChenDepartment of Histology & Embryology, School of Pre-clinical Medicine, Guangxi Medical University China ; Key Laboratory of School of Pre-clinical Medicine, Guangxi Medical University China.
Shao-Wen XiaoDepartment of Neurosurgery, First Affiliated Hospital, Guangxi Medical University China.
Xiao-Xun XieDepartment of Histology & Embryology, School of Pre-clinical Medicine, Guangxi Medical University China ; Key Laboratory of School of Pre-clinical Medicine, Guangxi Medical University China.
Guangxi Medical University · CNFirst Affiliated Hospital of GuangXi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer/testis (CT) antigens are normally expressed in testis and overexpressed in various tumor types. However, their biological function is largely unknown. OY-TES-1, one of cancer/testis (CT) antigens, is reported overexpression in hepatocellular carcinoma (HCC). And we assumed that OY-TES-1 contribute to oncogenesis and progression of HCC. In this study, we knocked down OY-TES-1 by small interference RNA (siRNA) in HCC cell lines (HepG2 and BEL-7404) to verify this assumption and evaluate its potential as therapeutic targets for HCC. We showed that down regulation of OY-TES-1 decreased cell growth, induced the G0/G1 arrest and apoptosis, and prevented migration and invasion in the two HCC cell lines. Further analysis revealed that down regulation of OY-TES-1 increased expression of apoptosis-regulated protein caspase-3, and decreased expression of cell cycle-regulated protein cyclin E, migration/invasion-regulated proteins MMP2 and MMP9. These findings may shed light on the gene therapy about the OY-TES-1 expression in HCC cells.

Indexed as

ApoptosisCarcinoma, HepatocellularCarrier ProteinsCaspase 3Cell CycleCell Cycle ProteinsCell Line, TumorCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticHumansLiver NeoplasmsMaleRNA, Small InterferingTestisACRBP protein, humanCarrier ProteinsCaspase 3Cell Cycle ProteinsRNA, Small InterferingCancer/testis antigenhepatocellular carcinomaOY-TES-1siRNA

Identifiers

PMID26339343
PMCPMC4555671
OpenAlexW2421953095

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.