Evidence map›Paper›PMID 29761918›Full record

ArticleJournal of cellular and molecular medicine2018

LncRNA HOXA11-AS promotes hepatocellular carcinoma progression by repressing miR-214-3p.

Meixiao Zhan, Ke He, Jing Xiao, Fei Liu, Haihe Wang, Zhenglin Xia, Xiaopeng Duan, Rui Huang, Yong Li, Xu He and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
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  3. lncRNA POLR2J4 Plays a Biomarker Role in Hepatitis B Virus-Related Hepatocellular Carcinoma Through Regulating miR-214-3p.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2024
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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

13 authors at 4 institutions in 1 country.

Meixiao ZhanCenter of Intervention radiology, Zhuhai Precision Medicine Center, Zhuhai People's Hospital, Zhuhai, Guangdong, China.
Ke HeDepartment of General Surgery, Guangdong Second Provincial General Hospital, Southern Medical University, Haizhu District, Guangzhou, Guangdong Province, China.
Jing XiaoCenter of Intervention radiology, Zhuhai Precision Medicine Center, Zhuhai People's Hospital, Zhuhai, Guangdong, China.
Fei LiuDepartment of General Surgery, Guangdong Second Provincial General Hospital, Southern Medical University, Haizhu District, Guangzhou, Guangdong Province, China.
Haihe WangDepartment of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong, China.
Zhenglin XiaDepartment of General Surgery, Guangdong Second Provincial General Hospital, Southern Medical University, Haizhu District, Guangzhou, Guangdong Province, China.
Xiaopeng DuanDepartment of General Surgery, Guangdong Second Provincial General Hospital, Southern Medical University, Haizhu District, Guangzhou, Guangdong Province, China.
Rui HuangDepartment of General Surgery, Guangdong Second Provincial General Hospital, Southern Medical University, Haizhu District, Guangzhou, Guangdong Province, China.
Yong LiCenter of Intervention radiology, Zhuhai Precision Medicine Center, Zhuhai People's Hospital, Zhuhai, Guangdong, China.
Xu HeCenter of Intervention radiology, Zhuhai Precision Medicine Center, Zhuhai People's Hospital, Zhuhai, Guangdong, China.
Hua YinCenter of Intervention radiology, Zhuhai Precision Medicine Center, Zhuhai People's Hospital, Zhuhai, Guangdong, China.
Guoan XiangDepartment of General Surgery, Guangdong Second Provincial General Hospital, Southern Medical University, Haizhu District, Guangzhou, Guangdong Province, China.ORCID http://orcid.org/0000-0002-7428-2253
Ligong LuCenter of Intervention radiology, Zhuhai Precision Medicine Center, Zhuhai People's Hospital, Zhuhai, Guangdong, China.
Zhuhai People's Hospital · CNSouthern Medical University · CNSun Yat-sen University · CNNanfang Hospital · CN

Funding

National Natural Science Foundation of China 81571785National Natural Science Foundation of China 81641110National Natural Science Foundation of China 81771957Natural Science Foundation of Guangdong Province, China 2015A030313725Natural Science Foundation of Guangdong Province, China 2016A030311055Natural Science Foundation of Guangdong Province, China 2016A030313770Science and Technology Foundation of Guangdong Province, China 2013B021800180Science and Technology Program of Guangzhou Province, China 201707010305Youth Science Fund of Guangdong Second Provincial General Hospital YQ2006-001
6 · The paper itself

Abstract

Accumulating studies supported that lncRNAs played important roles in tumorigenesis. LncRNA HOXA11-AS was a novel lncRNA that has been proved to involved in several tumours. However, the role of HOXA11-AS in the development of hepatocellular carcinoma (HCC) remains to be explained. In our study, we showed that HOXA11-AS expression was up-regulated in the HCC tissues, and the higher expression of HOXA11-AS was associated with the advanced stage in the HCC samples. In addition, we indicated that the expression of HOXA11-AS was up-regulated in HCC cell lines (Hep3B, SMMC-7721, MHCC97-H and BEL-7402) compared with normal liver cell lines (HL-7702). Overexpression of HOXA11-AS promoted HCC proliferation and invasion and induced the epithelial-mesenchymal transition (EMT) and knockdown of HOXA11-AS suppressed the HCC cell proliferation and invasion. However, we showed that miR-214-3p expression was down-regulated in the HCC tissues and cell lines. Ectopic expression of miR-214-3p suppressed HCC cell proliferation and invasion. Furthermore, we indicated that overexpression of HOXA11-AS decreased the miR-214-3p expression and the expression of miR-214-3p was negatively related with the HOXA11-AS expression in HCC samples. Ectopic expression of HOXA11-AS increased HCC proliferation and invasion and induced EMT through inhibiting miR-214-3p expression. These data suggested that HOXA11-AS/miR-214-3p axis was responsible for development of HCC.

Indexed as

hepatocellular carcinomaHOXA11-ASLncRNAmiR-214-3p

Identifiers

PMID29761918
PMCPMC6050501
OpenAlexW2884889442

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LicenceCC BY
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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.