Evidence map›Paper›PMID 27661126›Full record

ArticleOncotarget2016

MicroRNA-552 enhances metastatic capacity of colorectal cancer cells by targeting a disintegrin and metalloprotease 28.

Jian Wang, Hai Li, Yong Wang, Libin Wang, Xiurui Yan, Dong Zhang, Xiaoqiang Ma, Yong Du, Xiaoming Liu, Yinxue Yang

Abstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

10 authors.

Jian WangThe general hospital, Ningxia Medical University, Yinchuan 750004, China.
Hai LiDepartment of Colorectal Surgery, the General Hospital of Ningxia Medical University, Yinchuan 750004, China.
Yong WangThe general hospital, Ningxia Medical University, Yinchuan 750004, China.
Libin WangHuman Stem Cell Institute of the General Hospital at Ningxia Medical University, Yinchuan 750004, China.
Xiurui YanHuman Stem Cell Institute of the General Hospital at Ningxia Medical University, Yinchuan 750004, China.
Dong ZhangDepartment of Colorectal Surgery, the General Hospital of Ningxia Medical University, Yinchuan 750004, China.
Xiaoqiang MaDepartment of Colorectal Surgery, the General Hospital of Ningxia Medical University, Yinchuan 750004, China.
Yong DuThe general hospital, Ningxia Medical University, Yinchuan 750004, China.
Xiaoming LiuHuman Stem Cell Institute of the General Hospital at Ningxia Medical University, Yinchuan 750004, China.
Yinxue YangThe general hospital, Ningxia Medical University, Yinchuan 750004, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is one of the most common prevalent cancer types worldwide. MicroRNAs (miRNAs or miRs) have been demonstrated to play crucial roles in the development, metastasis and drug resistance of CRC. In the present study, a strikingly elevated expression of miR-552 was determined in CRC tumor tissues and cells by a miRNA profiling analysis. Importantly, the gene of A Disintegrin And Metalloprotease (ADAM) family member 28 (ADAM28) was identified as a target of miR-552, which was further validated in terms of genetic dual luciferase report assay. Furthermore, an inhibition of miR-552 in LOVE and LS174T CRC cells by transducing miR-552 inhibitor (antagomiR-552) with a lentiviral vector exhibited an ability to reduce cell proliferation, migration and clonogenicity. Moreover, both LOVO and LS174T cells stably expressing miR-552 inhibitor displayed a decreased ability to develop tumors in a murine xenograft model in vivo. In contrast, a knockdown of ADAM28 by short hairpin RNA could reverse the antagomiR-552-induced inhibition of metastatic features of CRC cells in vitro. These results suggested that miR-552 is an oncomir able to promote CRC metastasis in part through a mechanism of targeting ADAM28, which may be a novel target for CRC treatment and warrants for further investigation.

Indexed as

ADAM ProteinsAdultAgedAged, 80 and overAnimalsCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsFemaleHumansMaleMiceMicroRNAsMiddle AgedNeoplasm MetastasisADAM28 protein, humanADAM ProteinsMicroRNAsMIRN552 microRNA, humanMIRN592 microRNA, humanADAM28antagomircolorectal cancermicroRNAsmiR-552

Identifiers

PMID27661126
PMCPMC5342546

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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.