Evidence map›Paper›PMID 30122988›Full record

ArticleCancer management and research2018

LRH-1 drives hepatocellular carcinoma partially through induction of c-myc and cyclin E1, and suppression of p21.

Lijia Xiao, Yuliang Wang, Weicheng Liang, Liping Liu, Nannan Pan, Huimin Deng, Luqian Li, Chang Zou, Franky Leung Chan, Yiwen Zhou

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

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  15. Nuclear receptor NR5A2 negatively regulates cell proliferation and tumor growth in nervous system malignancies.Proceedings of the National Academy of Sciences of the United States of America · 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

10 authors at 4 institutions in 2 countries.

Lijia Xiao *Department of Clinical Laboratory Medicine, Shenzhen Hospital, Southern Medical University, Shenzhen, China, yiwenzhou21@126.com.
Yuliang Wang *School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, China, franky-chan@cuhk.edu.hk.
Weicheng LiangSchool of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, China, franky-chan@cuhk.edu.hk.
Liping LiuDepartment of Hepatobiliary and Pancreatic Surgery, The Second Clinical Medical College (Shenzhen People's Hospital), Jinan University, Shenzhen, China.
Nannan PanDepartment of Clinical Laboratory Medicine, Shenzhen Hospital, Southern Medical University, Shenzhen, China, yiwenzhou21@126.com.
Huimin DengDepartment of Clinical Laboratory Medicine, Shenzhen Hospital, Southern Medical University, Shenzhen, China, yiwenzhou21@126.com.
Luqian LiDepartment of Clinical Laboratory Medicine, Shenzhen Hospital, Southern Medical University, Shenzhen, China, yiwenzhou21@126.com.
Chang ZouClinical Medicine Research Center, Shenzhen Public Service Platform of Precision Medicine and Molecular Diagnosis on Tumor, The Second Clinical Medical College (Shenzhen People's Hospital), Jinan University, Shenzhen, China.
Franky Leung ChanSchool of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, China, franky-chan@cuhk.edu.hk.
Yiwen ZhouDepartment of Clinical Laboratory Medicine, Shenzhen Hospital, Southern Medical University, Shenzhen, China, yiwenzhou21@126.com.
Southern Medical University Shenzhen Hospital · CNChinese University of Hong Kong · HKJinan University · CNGuangdong Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo explore potential therapeutic target is one of the areas of great interest in both clinical and basic hepatocellular carcinoma (HCC) studies. Nuclear receptor liver receptor homolog-1 (LRH-1,

methodsThe LRH-1 expression level in HCC clinical samples was examined by immunohis-tochemistry (IHC). Stable LRH-1-suppressed HepG2 clones (HepG2

resultsWe confirmed that LRH-1 showed an increased expression pattern in HCC clinical samples. Our in vitro and in vivo results indicated that suppression of LRH-1 in HepG2 significantly attenuated its proliferation rate and tumorigenic capacity. Gene expression microarray analysis indicated that LRH-1mostly regulated gene expression involved in cell cycle. In addition, our gain-of-function experiments indicated that ectopic expression of LRH-1 dramatically induced the mRNA and protein levels of c-myc and cyclin E1, while attenuating the expression of p21.

conclusionOur results suggest that LRH-1 might be a potential therapeutic target for clinical HCC treatment.

Indexed as

c-myccyclin E1HCCLRH-1p21

Identifiers

PMID30122988
PMCPMC6078084
OpenAlexW2887668040

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.