Evidence map›Paper›PMID 22320217›Full record

ArticleCancer science2012

miR-30c-1* promotes natural killer cell cytotoxicity against human hepatoma cells by targeting the transcription factor HMBOX1.

Jiuyu Gong, Rongrong Liu, Ran Zhuang, Yun Zhang, Liang Fang, Zhuwei Xu, Liang Jin, Tao Wang, Chaojun Song, Kun Yang and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer science, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

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  18. MicroRNAs as Immunotherapy Targets for Treating Gastroenterological Cancers.Canadian journal of gastroenterology & hepatology · 2018
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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

14 authors at 1 institution in 1 country.

Jiuyu GongDepartment of Immunology, Fourth Military Medical University, Xi'an, China.
Rongrong Liu
Ran Zhuang
Yun Zhang
Liang Fang
Zhuwei Xu
Liang Jin
Tao Wang
Chaojun Song
Kun Yang
Yuying Wei
Angang Yang
Boquan Jin
Lihua Chen
Air Force Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells play a critical role in antitumor immunity, and the activation of NK cells is regulated by a series of NK cell receptors. Here, we show that crosslinking CD226, an important NK cell receptor, with the anti-CD226 mAb LeoA1 on NKL cells, regulated the expression of several microRNA and transmembrane tumor necrosis factor-α. Among them, miR-30c-1(*) was noticed because overexpression of miR-30c-1(*) triggered upregulation of transmembrane tumor necrosis factor-α expression and enhanced NK cell cytotoxicity against hepatoma cell lines SMMC-7721 and HepG2. Furthermore, we proved that the inhibitory transcription factor HMBOX1, which depressed the activation of NK cells, was the direct target gene of miR-30c-1(*). In conclusion, our results revealed a novel regulatory mechanism: miR-30c-1(*) promoted NK cell cytotoxicity against hepatoma cells by targeting HMBOX1.

Indexed as

AnimalsAntigens, Differentiation, T-LymphocyteCarcinoma, HepatocellularCell Line, TumorCytotoxicity, ImmunologicFemaleHomeodomain ProteinsHumansKiller Cells, NaturalLiver NeoplasmsMiceMicroRNAsT Lineage-Specific Activation Antigen 1Tumor Necrosis Factor-alphaAntigens, Differentiation, T-LymphocyteHMBOX1 protein, humanHomeodomain ProteinsMicroRNAsMIRN30b microRNA, humanT Lineage-Specific Activation Antigen 1Tumor Necrosis Factor-alpha

Identifiers

PMID22320217
PMCPMC7659379
OpenAlexW2069357915

What OpenQuestion holds

Textmetadata
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.