Evidence map›Paper›PMID 25549355›Full record

Trial reportPloS one2014

RETRACTED: miR-150-5p inhibits hepatoma cell migration and invasion by targeting MMP14.

Tao Li, Junjie Xie, Chuan Shen, Dongfeng Cheng, Yuan Shi, Zhichong Wu, Qian Zhan, Xiaxing Deng, Hao Chen, Baiyong Shen and 3 more

RetractedOpen access · goldAbstract readClinical TrialRetracted Publication
In one paragraph

Trial report in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

47 citing papers in PubMed, 82 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Tao LiDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Junjie XieDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Chuan ShenDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Dongfeng ChengDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Yuan ShiDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Zhichong WuDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Qian ZhanDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Xiaxing DengDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Hao ChenDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Baiyong ShenDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Chenghong PengDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Hongwei LiDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Zhecheng ZhuDepartment of Hepato-Bilio-Pancreatic Surgery, Shanghai Institute of Digestive Surgery, Rui Jin Hospital affiliated with Shanghai Jiaotong University, Ruijin er Road, No. 197, 200025, Shanghai, People's Republic of China.
Ruijin Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related mortality worldwide. Despite progress in diagnostics and treatment of HCC, its prognosis remains poor because the molecular mechanisms underlying hepatocarcinogenesis are not well understood. In the study, we focused on identifying the role of miRNAs in HCC progression. miRNA microarray was used to analyze the differentially expressed miRNAs, and the results were validated by qPCR. We found that the miR-150-5p expression is down-regulated in HCC tissues compared with pair non-tumor tissues. miR-150-5p expression is also decreased in metastatic cancer tissues compared with pair primary tissues, indicating that miR-150-5p may be involved in HCC metastasis. Functionally, miR-150-5p inhibition significantly promotes hepatoma cell migration and invasion, whereas miR-150-5p overexpression suppresses cancer cell migration and invasion in vitro. The matrix metalloproteinase 14 (MMP14) is identified as a new target gene of miR-150-5p. miR-150-5p markedly inhibits MMP14 expression in hepatoma cells, and miR-150-5p expression is negative correlation with MMP14 expression in vivo. More important, re-expression of MMP14 in hepatoma cells partially reverses the effect of miR-150-5p in inhibiting cell invasion.

Indexed as

Cell MovementAdultAgedCarcinoma, HepatocellularFemaleGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticHep G2 CellsHumansLiver NeoplasmsMaleMatrix Metalloproteinase 14MicroRNAsMiddle AgedNeoplasm InvasivenessNeoplasm ProteinsMatrix Metalloproteinase 14MicroRNAsMIR150, humanMMP14 protein, humanNeoplasm ProteinsRNA, Neoplasm

Identifiers

PMID25549355
PMCPMC4280173
OpenAlexW2073257981

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.