Evidence map›Paper›PMID 27704356›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

MicroRNA-27b exerts an oncogenic function by targeting Fbxw7 in human hepatocellular carcinoma.

Xin-Fang Sun, Jin-Ping Sun, Hong-Tao Hou, Ke Li, Xin Liu, Quan-Xing Ge

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

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  13. MicroRNA‑223‑induced inhibition of theMolecular medicine reports · 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

6 authors at 1 institution in 1 country.

Xin-Fang SunDepartment of Gastroenterology, Huaihe Hospital, Henan University, No. 8 Baobei Road, Kaifeng, Henan Province, 475000, China.
Jin-Ping SunDepartment of Gastroenterology, Huaihe Hospital, Henan University, No. 8 Baobei Road, Kaifeng, Henan Province, 475000, China.
Hong-Tao HouDepartment of Gastroenterology, Huaihe Hospital, Henan University, No. 8 Baobei Road, Kaifeng, Henan Province, 475000, China.
Ke LiDepartment of Gastroenterology, Huaihe Hospital, Henan University, No. 8 Baobei Road, Kaifeng, Henan Province, 475000, China.
Xin LiuDepartment of Gastroenterology, Huaihe Hospital, Henan University, No. 8 Baobei Road, Kaifeng, Henan Province, 475000, China.
Quan-Xing GeDepartment of Gastroenterology, Huaihe Hospital, Henan University, No. 8 Baobei Road, Kaifeng, Henan Province, 475000, China. gequan_xing@163.com.
Henan University Huaihe Hospital and Huaihe Clinical Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant expression of microRNAs (miRNAs) plays fundamental effect on the pathogenesis of hepatocellular carcinoma (HCC). MiR-27b was previously found to play important roles in human cancers. However, its expression status, clinical significance, and biological functions in HCC remain largely unclear. The expression status of miR-27b in HCC specimens and cells were determined with qRT-PCR. MTT, 5-bromodeoxyuridine (BrdU) proliferation assays, and flow cytometry analysis were carried out to assay proliferation, cell cycle, and apoptosis. A subcutaneous model was used to evaluated the HCC tumor growth in vivo. The putative target gene of miR-27b was disclosed by TargetScan and a luciferase reporter assay. The levels of miR-27b were overexpressed in HCC. Overexpression of miR-27b was correlated with adverse prognostic features and reduced survival rate. Inhibition of miR-27b in SMMC-7721 cells remarkably suppressed proliferative ability and cell-cycle progression while enhanced apoptosis. In contrast, miR-27b overexpression resulted in prominent increased proliferation and process of cell cycle and reduced apoptosis of Hep3B cells. In vivo studies showed that knockdown of miR-27b inhibited the in vivo growth of SMMC-7721 cells in mouse xenograft model. Furthermore, we confirmed that Fbxw7 was directly regulated by miR-27b and mediated the roles of miR-27b in HCC. We suggest that miR-27b serves as an oncogenic miRNA in HCC by modulating proliferation, cell-cycle progression, and apoptosis, and its oncogenic effect is mediated by its downstream target gene, Fbxw7.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisBiomarkers, TumorBlotting, WesternCarcinoma, HepatocellularCell CycleCell Cycle ProteinsCell ProliferationF-Box ProteinsF-Box-WD Repeat-Containing Protein 7FemaleHumansLiver NeoplasmsMaleMiceBiomarkers, TumorCell Cycle ProteinsF-Box ProteinsF-Box-WD Repeat-Containing Protein 7FBXW7 protein, humanMicroRNAsMIRN27 microRNA, humanRNA, MessengerUbiquitin-Protein LigasesCell growthFbxw7Hepatocellular carcinomaMicroRNA-27bOncogenic microRNA

Identifiers

PMID27704356
OpenAlexW2528384754

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.