Evidence map›Paper›PMID 25232379›Full record

ArticleInternational journal of clinical and experimental medicine2014

miR-148b functions as a tumor suppressor in non-small cell lung cancer by targeting carcinoembryonic antigen (CEA).

Guo-Long Liu, Xia Liu, Xiao-Bin Lv, Xiao-Pai Wang, Xi-Sheng Fang, Yi Sang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

  1. Identification of potential core genes and miRNAs in pediatric ACCIntractable & rare diseases research · 2022
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  5. Efficacy of Huaier granule in patients with breast cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2019
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  16. Downregulation of miR-148b as biomarker for early detection of hepatocellular carcinoma and may serve as a prognostic marker.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
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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 2 institutions in 1 country.

Guo-Long LiuDepartment of Oncology, Guangzhou First Municipal People's Hospital Affiliated to Guangzhou Medical College 1 Panfu Road, Guangzhou, P. R. China.
Xia LiuDepartment of Oncology, Guangzhou First Municipal People's Hospital Affiliated to Guangzhou Medical College 1 Panfu Road, Guangzhou, P. R. China.
Xiao-Bin LvKey Laboratory of Malignant Tumor Gene Regulation and Target Therapy of Guangdong Higher Education Institutes, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University 107 Yanjiang West Road, Guangzhou, P. R. China ; Research Center of Medicine, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University 107 Yanjiang West Road, Guangzhou, P. R. China.
Xiao-Pai WangDepartment of Pathology, Guangzhou First Municipal People's Hospital Affiliated to Guangzhou Medical College 1 Panfu Road, Guangzhou, P. R. China.
Xi-Sheng FangDepartment of Oncology, Guangzhou First Municipal People's Hospital Affiliated to Guangzhou Medical College 1 Panfu Road, Guangzhou, P. R. China.
Yi SangState Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center Guangzhou 510060, China.
Guangzhou First People's Hospital · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant expression of miR-148b has been found in several types of cancer, but its expression and potential biologic role in non-small cell lung cancer (NSCLC) are still largely unknown. Here, we found that miR-148b was commonly under-expressed in human non-small celllung cancer (NSCLC) specimens and cell lines. The overexpression of miR-148b dramatically suppressed NSCLC cell proliferation and migration. Furthermore, miR-148b could regulate carcinoembryonic antigen (CEA) expression by luciferase reporter assay. On the other hand, CEA was widely up-regulated in NSCLC specimens, and its mRNA levels were inversely correlated with miR-148b expression. These suggest that CEA expression may be regulated by miR-148b. Collectively, our findings indicate miR-148b is low expression in NSCLC cells, which results in CEA overexpression and disease progression in NSCLC patients.

Indexed as

CEAmigrationmiR-148bNSCLCtumor suppressors

Identifiers

PMID25232379
PMCPMC4161539
OpenAlexW2260269675

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.