Evidence map›Paper›PMID 30679629›Full record

ArticleScientific reports2019

High Expression of long non-coding RNA PVT1 predicts metastasis in Han and Uygur Patients with Gastric Cancer in Xinjiang, China.

Xianxian Ren, Dongdong Cao, Li Yang, Xia Li, Wei Zhang, Yongbiao Xiao, Yu Xi, Feng Li, Dongmei Li, Zemin Pan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. lncRNA PVT1: a novel oncogene in multiple cancers.Cellular & molecular biology letters · 2022
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Non-coding RNAs underlying chemoresistance in gastric cancer.Cellular oncology (Dordrecht, Netherlands) · 2020
    Review
  9. Review
  10. Article
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

10 authors at 3 institutions in 1 country.

Xianxian RenSchool of Medicine, Shihezi University, Shihezi, Xinjiang, China.
Dongdong CaoSchool of Medicine, Shihezi University, Shihezi, Xinjiang, China.
Li YangSchool of Medicine, Shihezi University, Shihezi, Xinjiang, China.
Xia LiSchool of Medicine, Shihezi University, Shihezi, Xinjiang, China.
Wei ZhangFirst Affiliated Hospital of Shihezi University, Shihezi, Xinjiang, China.
Yongbiao XiaoFirst People's Hospital of Kashi, Kashi, Xinjiang, China.
Yu XiFirst Affiliated Hospital of Shihezi University, Shihezi, Xinjiang, China.
Feng LiSchool of Medicine, Shihezi University, Shihezi, Xinjiang, China.
Dongmei LiSchool of Medicine, Shihezi University, Shihezi, Xinjiang, China. lidong_abc@126.com.
Zemin PanSchool of Medicine, Shihezi University, Shihezi, Xinjiang, China. panteacher89@sina.com.
Shihezi University · CNFirst Affiliated Hospital of Shihezi University Medical College · CNBeijing Chao-Yang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To analyze the level and diagnostic value of plasmacytoma variant translocation 1 (PVT1) in gastric cancer (GC) of Han and Uygur in Xinjiang, China, we collected 42 GC and 47 normal gastric tissues and performed tissue microarray. In situ hybridization was used to detect PVT1, while immunohistochemistry was used to analyze c-myc. The relationship between PVT1, c-myc and clinical pathological features was investigated. We then analyzed the expression of PVT1 in six GC cell lines. RNA interference was used to silence PVT1 in BGC823 and AGS cells. c-myc was detected by western blotting after silencing PVT1, while proliferation, invasion and migration ability were also analyzed. We found that PVT1 and c-myc were highly expressed in both Han and Uygur GC tissues. In Han GC, PVT1 was correlated with lymph node metastasis and primary tumor site. In Uygur GC, both PVT1 and c-myc were correlated with lymph node metastasis and clinical staging. PVT1 was positively correlated with c-myc. BGC823 and AGS cells exhibited high levels of PVT1. When PVT1 expression was silenced, the expression of c-myc decreased, while migration and invasion ability were also decreased in cells. PVT1 could therefore be a potential biomarker to predict the metastatic tendency of GC in both Han and Uygur patients.

Indexed as

EthnicityBiomarkers, TumorCell Line, TumorCell MovementCell ProliferationChinaFemaleGene Expression Regulation, NeoplasticHumansImmunohistochemistryIn Situ HybridizationLymphatic MetastasisLymph NodesMaleMiddle AgedPrognosisBiomarkers, TumorMYC protein, humanProto-Oncogene Proteins c-mycPVT1 long-non-coding RNA, humanRNA, Long Noncoding

Identifiers

PMID30679629
PMCPMC6345741
OpenAlexW2919930374

What OpenQuestion holds

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LicenceCC BY
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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.