Evidence map›Paper›PMID 29435409›Full record

ArticleFEBS open bio2018

miR-204-5p suppresses hepatocellular cancer proliferation by regulating homeoprotein SIX1 expression.

Yi Chu, Mingzuo Jiang, Feng Du, Di Chen, Tao Ye, Bing Xu, Xiaowei Li, Weijie Wang, Zhaoyan Qiu, Haiming Liu and 3 more

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

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  13. Investigation the Role of Autophagy in Non-Small Cell Lung Cancer.Asian Pacific journal of cancer prevention : APJCP · 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

13 authors at 3 institutions in 1 country.

Yi ChuState Key Laboratory of Cancer Biology & Institute of Digestive Diseases Xijing Hospital The Fourth Military Medical University Xi'an China.
Mingzuo JiangState Key Laboratory of Cancer Biology & Institute of Digestive Diseases Xijing Hospital The Fourth Military Medical University Xi'an China.
Feng DuState Key Laboratory of Cancer Biology & Institute of Digestive Diseases Xijing Hospital The Fourth Military Medical University Xi'an China.
Di ChenState Key Laboratory of Cancer Biology & Institute of Digestive Diseases Xijing Hospital The Fourth Military Medical University Xi'an China.
Tao YeState Key Laboratory of Military Stomatology National Clinical Research Center for Oral Diseases Shannxi key Laboratory of Oral Diseases School of Stomatology The Fourth Military Medical University Xi'an China.
Bing XuState Key Laboratory of Cancer Biology & Institute of Digestive Diseases Xijing Hospital The Fourth Military Medical University Xi'an China.
Xiaowei LiState Key Laboratory of Cancer Biology & Institute of Digestive Diseases Xijing Hospital The Fourth Military Medical University Xi'an China.
Weijie WangState Key Laboratory of Cancer Biology & Institute of Digestive Diseases Xijing Hospital The Fourth Military Medical University Xi'an China.
Zhaoyan QiuDepartment of General Surgery the General Hospital of the people's Liberation Army Beijing China.
Haiming LiuCollege of Computer Science and Technology Symbolic Computation and Knowledge Engineering of Ministry of Education Jilin University Changchun China.
Yongzhan NieState Key Laboratory of Cancer Biology & Institute of Digestive Diseases Xijing Hospital The Fourth Military Medical University Xi'an China.
Jie LiangState Key Laboratory of Cancer Biology & Institute of Digestive Diseases Xijing Hospital The Fourth Military Medical University Xi'an China.
Daiming FanState Key Laboratory of Cancer Biology & Institute of Digestive Diseases Xijing Hospital The Fourth Military Medical University Xi'an China.
Xijing Hospital · CNAir Force Medical University · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fewer than 30% of patients with hepatocellular carcinoma (HCC) are eligible to receive curative therapies, and so a better understanding of the molecular mechanisms of HCC is needed to identify potential therapeutic targets. The role of microRNA (miRNA) in modulating tumour progression has been demonstrated, and therapies targeting miRNA appear promising. miR-204-5p has been shown to function in numerous types of cancer, but its role in HCC remains unclear. In this study, we found that miR-204-5p expression was downregulated in cancerous HCC tissues compared to nontumour tissues. Kaplan-Meier survival curve analysis also showed that low expression of miR-204-5p predicted worse outcomes of HCC patients. In addition, miR-204-5p expression was significantly lower in HCC cell lines. The function of miR-204-5p was also assessed both

Indexed as

cell cycleHCC proliferationmiR‐204‐5pSIX1

Identifiers

PMID29435409
PMCPMC5794460
OpenAlexW2772819648

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.