Evidence map›Paper›PMID 32044726›Full record

ArticleMolecular therapy. Nucleic acids2020

miR-552 Regulates Liver Tumor-Initiating Cell Expansion and Sorafenib Resistance.

Tao Han, Yue Zhang, Xiaodan Yang, Lei Han, Hengyu Li, Tingsong Chen, Zhendong Zheng

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 41 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Tao HanDepartment of Oncology, General Hospital of Northern Theater Command, Shenyang, 110016 Liaoning Province, China; Department of Oncology, Second Affiliated Hospital of Dalian Medical University, Dalian, 116023, Liaoning Province, China.
Yue ZhangDepartment of Oncology, General Hospital of Northern Theater Command, Shenyang, 110016 Liaoning Province, China; Graduate School, Jinzhou Medical University, Jinzhou, 121000 Liaoning Province, China.
Xiaodan YangDepartment of Oncology, General Hospital of Northern Theater Command, Shenyang, 110016 Liaoning Province, China.
Lei HanDepartment of Hepatobiliary Surgery, General Hospital of Northern Theater Command, Shenyang, 110016 Liaoning Province, China.
Hengyu LiDepartment of Breast and Thyroid Surgery, First Affiliated Hospital of Second Military Medical University, 200433 Shanghai, China. Electronic address: lhy@smmu.edu.cn.
Tingsong ChenDepartment of Cancer Intervention, Shanghai Seventh People's Hospital, 200001 Shanghai, China. Electronic address: cts552052597@163.com.
Zhendong ZhengDepartment of Oncology, General Hospital of Northern Theater Command, Shenyang, 110016 Liaoning Province, China. Electronic address: zhengzhdong@163.com.
General Hospital of Shenyang Military Region · CNJinzhou Medical University · CNSecond Military Medical University · CNSeventh People's Hospital of Shanghai · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are involved in tumorigenesis, progression, recurrence, and drug resistance of hepatocellular carcinoma (HCC). However, few miRNAs have been identified and entered clinical practice. Herein, we report that microRNA (miR)-552 is upregulated in HCC tissues and has an important function in liver tumor-initiating cells (T-ICs). Functional studies revealed that a forced expression of miR-552 promotes liver T-IC self-renewal and tumorigenesis. Conversely, miR-552 knockdown inhibits liver T-IC self-renewal and tumorigenesis. Mechanistically, miR-552 downregulates phosphatase and tensin homolog (PTEN) via its mRNA 3' UTR and activates protein kinase B (AKT) phosphorylation. Our clinical investigations elucidated the prognostic value of miR-552 in HCC patients. Furthermore, miR-552 expression determines the responses of hepatoma cells to sorafenib treatment. The analysis of patient cohorts and patient-derived xenografts (PDXs) further demonstrated that miR-552 may predict sorafenib benefits in HCC patients. In conclusion, our findings revealed the crucial role of the miR-552 in liver T-IC expansion and sorafenib response, rendering miR-552 an optimal target for the prevention and intervention in HCC.

Indexed as

hepatocellular carcinomamiR-552PTENsorafenibtumor-initiating cells

Identifiers

PMID32044726
PMCPMC7015836
OpenAlexW2999702843

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.