Evidence map›Paper›PMID 30891870›Full record

ArticleCancer science2019

Hepatitis B virus-regulated growth of liver cancer cells occurs through the microRNA-340-5p-activating transcription factor 7-heat shock protein A member 1B axis.

Feifei Song, Mingcong Wei, Jingwen Wang, Yang Liu, Mingxiong Guo, Xiaolu Li, Jun Luo, Junying Zhou, Min Wang, Deyin Guo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

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  14. Epigenetic Alterations of Heat Shock Proteins (HSPs) in Cancer.International journal of molecular sciences · 2019
    Review
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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

12 authors at 3 institutions in 1 country.

Feifei SongSchool of Basic Medical Sciences, Wuhan University, Wuhan, China.
Mingcong WeiSchool of Basic Medical Sciences, Wuhan University, Wuhan, China.
Jingwen WangSchool of Basic Medical Sciences, Wuhan University, Wuhan, China.
Yang LiuSchool of Basic Medical Sciences, Wuhan University, Wuhan, China.
Mingxiong GuoHubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University, Wuhan, China.
Xiaolu LiDepartment of Radiation Oncology, Hubei Cancer Hospital, Wuhan, China.
Jun LuoZhongnan Hospital of Wuhan University, Wuhan, China.
Junying ZhouZhongnan Hospital of Wuhan University, Wuhan, China.
Min WangSchool of Basic Medical Sciences, Wuhan University, Wuhan, China.
Deyin GuoSchool of Medicine, Sun Yat-sen University, Guangdong, China.
Lang ChenSchool of Basic Medical Sciences, Wuhan University, Wuhan, China.
Guihong SunSchool of Basic Medical Sciences, Wuhan University, Wuhan, China.ORCID https://orcid.org/0000-0003-4451-7135
Wuhan University · CNHubei Cancer Hospital · CNSun Yat-sen University · CN

Funding

Hubei Provincial Science & Technology Innovation Team grant 2015CFA009National Natural Science Foundation of China 31370187National Natural Science Foundation of China 31741081National Natural Science Foundation of China 31871427National Natural Science Foundation of China 81572006National Natural Science Foundation of China 81572447National Natural Science Foundation of China 81772839
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a common cancer with poor prognosis. Hepatitis B virus (HBV) is one of the leading causes of HCC, but the precise mechanisms by which this infection promotes cancer development are not fully understood. Recently, miR-340-5p, a microRNA (miRNA) that has been identified as a cancer suppressor gene, was found to inhibit the migration and invasion of liver cancer cells. However, the effect of miR-340-5p on cell proliferation and apoptosis in HBV-associated HCC remains unknown. In our study, we show that miR-340-5p plays an important role during HBV infection and hepatocellular carcinoma development. Specifically, this miRNA directly binds to the mRNA encoding activating transcription factor 7 (ATF7), a protein that both promotes cell proliferation and suppresses apoptosis through its interaction with heat shock protein A member 1B (HSPA1B). We further found that miR-340-5p is downregulated by HBV, which enhances ATF7 expression, leading to enhanced cell proliferation and inhibition of apoptosis. Notably, ATF7 is upregulated in HCC tissue, suggesting that HBV may target miR-340-5p in vivo to promote ATF7/HSPA1B-mediated proliferation and apoptosis and regulate liver cancer progression. This work helps to elucidate the complex interactions between HBV and host miRNAs and further suggests that miR-340-5p may represent a promising candidate for the development of improved therapeutic strategies for HCC.

Indexed as

Activating Transcription FactorsApoptosisCarcinoma, HepatocellularCell Line, TumorCell ProliferationDisease ProgressionGene Expression ProfilingGene Expression Regulation, NeoplasticHepatitis BHep G2 CellsHSP70 Heat-Shock ProteinsHumansLiver NeoplasmsMicroRNAsActivating Transcription FactorsATF7 protein, humanHSP70 Heat-Shock ProteinsHSPA1B protein, humanMicroRNAsMIRN340 microRNA, humanapoptosisATF7HBV-related HCCmiR-340-5pproliferation

Identifiers

PMID30891870
PMCPMC6501011
OpenAlexW2924355051

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.