Evidence map›Paper›PMID 26980572›Full record

ArticleJournal of experimental & clinical cancer research : CR2016

MicroRNA-203 suppresses gastric cancer growth by targeting PIBF1/Akt signaling.

Shao-Jun Chu, Ge Wang, Peng-Fei Zhang, Rui Zhang, Yan-Xia Huang, Yun-Min Lu, Wei Da, Qun Sun, Jing Zhang, Jin-Shui Zhu

RetractedAbstract readRetracted Publication
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2016. 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 It has been retracted, and should not be counted.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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–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

11 citing papers in PubMed.

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  3. Diagnostic and prognostic significance of serum miR-203 in patients with acute myeloid leukemia.International journal of clinical and experimental pathology · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Shao-Jun ChuDepartment of Gerontology, Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital, Shanghai, 200233, China.
Ge WangDepartment of Gastroenterology, Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital, Yishan Road No. 600, Shanghai, 200233, China.
Peng-Fei ZhangDepartment of Gastroenterology, Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital, Yishan Road No. 600, Shanghai, 200233, China.
Rui ZhangDepartment of Gastroenterology, Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital, Yishan Road No. 600, Shanghai, 200233, China.
Yan-Xia HuangDepartment of Gastroenterology, Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital, Yishan Road No. 600, Shanghai, 200233, China.
Yun-Min LuDepartment of Gastroenterology, Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital, Yishan Road No. 600, Shanghai, 200233, China.
Wei DaDepartment of Gastroenterology, Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital, Yishan Road No. 600, Shanghai, 200233, China.
Qun SunDepartment of Gastroenterology, Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital, Yishan Road No. 600, Shanghai, 200233, China.
Jing ZhangDepartment of Gastroenterology, Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital, Yishan Road No. 600, Shanghai, 200233, China. jing5522724@163.com.
Jin-Shui ZhuDepartment of Gastroenterology, Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital, Yishan Road No. 600, Shanghai, 200233, China. zhujs1803@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) have been proved involved in many tumorigenic behaviors including tumor growth. But, the clinical significance and functions of miRNA-203 in gastric cancer (GC) remain elusive.

resultsDecreased expression of miRNA-203 was correlated with tumor size, poor prognosis and recurrence in GC patients. Overexpression of miR-203 or knockdown of its target progesterone immunomodulatory binding factor 1 (PIBF1) inhibited GC growth in vitro and in vivo, while miR-203 knockdown promoted GC proliferation. In addition, PIBF1 overexpression attenuated the inhibitory effects of miR-203 on GC growth and enhanced that effect on p-Akt expression.

conclusionsMiR-203 as a tumor biomarker suppresses GC growth through targeting the PIBF1/Akt signaling, suggesting that it may have the important therapeutic potential for the treatment of GC.

Indexed as

Cell Line, TumorCell ProliferationFemaleHumansMaleMicroRNAsNeoplasm Recurrence, LocalPregnancy ProteinsPrognosisProto-Oncogene Proteins c-aktSignal TransductionStomach NeoplasmsSuppressor Factors, ImmunologicMicroRNAsMIRN203 microRNA, humanPIBF1 protein, humanPregnancy ProteinsProto-Oncogene Proteins c-aktSuppressor Factors, ImmunologicAktGastric cancerGrowthmiRNA-203PIBF1

Identifiers

PMID26980572
PMCPMC4791790

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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.