Evidence map›Paper›PMID 30982498›Full record

ArticleOncology research2019

High Blood miR-802 Is Associated With Poor Prognosis in HCC Patients by Regulating DNA Damage Response 1 (REDD1)-Mediated Function of T Cells.

Chao Jiang, Xueyan Liu, Meng Wang, Guoyue Lv, Guangyi Wang

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Oncology research, 2019. 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 It has been retracted, and should not be counted.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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. A Review of Emerging Biomarkers for Immune Checkpoint Inhibitors in Tumors of the Gastrointestinal Tract.Medical science monitor : international medical journal of experimental and clinical research · 2022
    Review
  4. MicroRNA-802 promotes the progression of osteosarcoma through targeting p27 and activating PI3K/AKT pathway.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Article
  5. Dysfunction of miR-802 in tumors.Journal of clinical laboratory analysis · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Chao JiangDepartment of Hepatobiliary Pancreatic Surgery, First Hospital of Jilin University, Changchun, P.R. China.
Xueyan LiuDepartment of Cardiology, China-Japan Union Hospital of Jilin University, Changchun, P.R. China.
Meng WangDepartment of Hepatobiliary Pancreatic Surgery, First Hospital of Jilin University, Changchun, P.R. China.
Guoyue LvDepartment of Hepatobiliary Pancreatic Surgery, First Hospital of Jilin University, Changchun, P.R. China.
Guangyi WangDepartment of Hepatobiliary Pancreatic Surgery, First Hospital of Jilin University, Changchun, P.R. China.
First Hospital of Jilin University · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

miR-802 has been reported to be dysregulated in multiple tumors and contribute to tumor progression. However, its role in HCC was still largely unknown. The aim of this study is to investigate the function and mechanism of miR-802 in HCC progression. The results showed that miR-802 was upregulated in the peripheral blood and tumor tissue of HCC patients, and high levels of blood miR-802 predicted poor prognosis. miR-802 had no effect on the proliferation and migration of HCC cell lines. Interestingly, the levels of CD8/CD28 and regulated in development and DNA damage response 1 (REDD1) were declined along with the upregulation of miR-802 in vivo. Hence, it is speculated that miR-802 participated in the regulation of T-cell function in HCC patients. Furthermore, we demonstrated that mir-802 directly targets REDD1 and inhibited its expression. miR-802 increased the expression of programmed cell death protein 1 (PD-1) and decreased the expression of interferon-γ (IFN-γ) and CD8

Indexed as

DNA DamageCarcinoma, HepatocellularCell Line, TumorCell SurvivalDisease ProgressionHEK293 CellsHumansInterferon-gammaLiver NeoplasmsMicroRNAsNeoplasm InvasivenessPrognosisProgrammed Cell Death 1 ReceptorT-LymphocytesTranscription FactorsUp-RegulationDDIT4 protein, humanInterferon-gammaMicroRNAsMIRN802 microRNA, humanPDCD1 protein, humanProgrammed Cell Death 1 ReceptorTranscription Factors

Identifiers

PMID30982498
PMCPMC7848258
OpenAlexW2939192576

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.