Evidence map›Paper›PMID 32419651›Full record

ArticleTechnology in cancer research & treatment

miR-3196 acts as a Tumor Suppressor and Predicts Survival Outcomes in Patients With Gastric Cancer.

Guo Chen, Jinliang Wan, Zhenbo Wang, Lei Li, Hongying Jia, Shaozhi Xing, Shaoshui Chen, Xiaocheng Fan, Rui Li

Open access · goldAbstract read
In one paragraph

Article in Technology in cancer research & treatment. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Differential Expression of Small Non-Coding RNAs in Uterine Leiomyomas.International journal of molecular sciences · 2025
    Article
  3. International journal of molecular sciences · 2023
    Review
  4. Article
  5. Review
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

9 authors at 2 institutions in 1 country.

Guo ChenDepartment of Oncology, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Jinliang WanDepartment of Oncology, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Zhenbo WangDepartment of Oncology, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Lei LiDepartment of Oncology, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Hongying JiaOperating Room, People's Hospital of Yangxin County, Binzhou, Shandong, China.
Shaozhi XingDepartment of Oncology, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Shaoshui ChenDepartment of Oncology, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Xiaocheng FanDepartment of Oncology, Binzhou Medical University Hospital, Binzhou, Shandong, China.ORCID 0000-0003-0852-2260
Rui LiDepartment of Ultrasound, Binzhou Medical University Hospital, Binzhou, Shandong, China.ORCID 0000-0002-6643-5387
Binzhou Medical University · CNPeople's Hospital of Yangzhong · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric cancer is one of the most common malignancies worldwide with high mortality. Therefore, identifying cancer-related biomarkers for predicting prognosis and progression of gastric cancer is essential. This study aimed to investigate the clinical value and functional role of microRNA-3196 in gastric cancer.

methodsThe relative expression levels of microRNA-3196 in gastric cancer tissues and adjacent normal tissues were detected by quantitative reverse transcription-polymerase chain reaction. In this study, quantitative reverse transcription-polymerase chain reaction, cell proliferation assay, and Transwell migration and invasion assays were performed to explore microRNA-3196 expression level and its effects on cell proliferation, migration, and invasion in gastric cancer cells. The Kaplan-Meier method and multivariate Cox regression analyses were used to explore the prognostic significance of microRNA-3196 in gastric cancer. Dual-luciferase report assay was performed to validate the potential target gene regulated by microRNA-3196 in gastric cancer.

resultsThe expression of microRNA-3196 was downregulated in gastric cancer tissues and cell lines. Downregulation of microRNA-3196 was associated with lymph node metastasis and Tumor Node Metastasis (TNM) stage. The Kaplan-Meier curve analysis indicated that patients with low expression of microRNA-3196 had a poor prognosis, and the Cox regression analysis results showed microRNA-3196 expression was an independent prognostic factor of gastric cancer. Moreover, overexpression of microRNA-3196 inhibited cell proliferation, migration, and invasion, while knockdown of microRNA-3196 promoted these cellular behaviors in AGS and MKN45 cells. OTX1 may be a potential target gene regulated by microRNA-3196 in gastric cancer.

conclusionsThese results suggested that microRNA-3196 might not only a tumor suppressor in gastric cancer cells by modulating OTX1 but also might be an independent prognostic biomarker and therapeutic target of gastric cancer.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisBiomarkers, TumorCell MovementCell ProliferationFemaleGastrectomyHumansMaleMicroRNAsMiddle AgedNeoplasm InvasivenessOtx Transcription FactorsPrognosisStomach NeoplasmsSurvival RateBiomarkers, TumorMicroRNAsMIRN3196 microRNA, humanOTX1 protein, humanOtx Transcription Factorsgastric cancerinvasionmigrationmiR-3196prognosisproliferation

Identifiers

PMID32419651
PMCPMC7235653
OpenAlexW3027483948

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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.