Evidence map›Paper›PMID 30643007›Full record

ArticleBioscience reports2019

LncRNA TP73-AS1 sponges miR-141-3p to promote the migration and invasion of pancreatic cancer cells through the up-regulation of BDH2.

Xian-Ping Cui, Chuan-Xi Wang, Zhi-Yi Wang, Jian Li, Ya-Wen Tan, Song-Tao Gu, Cheng-Kun Qin

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
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  9. Review
  10. Upregulation of Neural Cell Adhesion Molecule 1 (NCAM1) by hsa-miR-141-3p Suppresses Ameloblastoma Cell Migration.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
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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

7 authors at 1 institution in 1 country.

Xian-Ping CuiDepartment of Hepatobiliary Surgery, Provincial Hospital affiliated to Shandong University, Jinan 250021, China cuixping@163.com Qinchengkun@medmail.com.cn.ORCID 0000-0002-0572-3895
Chuan-Xi WangDepartment of Oncology, Provincial Hospital affiliated to Shandong University, Jinan 250021, China.
Zhi-Yi WangDepartment of Hepatobiliary Surgery, Provincial Hospital affiliated to Shandong University, Jinan 250021, China.
Jian LiDepartment of Hepatobiliary Surgery, Provincial Hospital affiliated to Shandong University, Jinan 250021, China.
Ya-Wen TanDepartment of Hepatobiliary Surgery, Provincial Hospital affiliated to Shandong University, Jinan 250021, China.
Song-Tao GuDepartment of Hepatobiliary Surgery, Provincial Hospital affiliated to Shandong University, Jinan 250021, China.
Cheng-Kun QinDepartment of Hepatobiliary Surgery, Provincial Hospital affiliated to Shandong University, Jinan 250021, China cuixping@163.com Qinchengkun@medmail.com.cn.
Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

LncRNA TP73 antisense RNA 1T (TP73-AS1) plays an important role in human malignancies. However, the levels of TP73-AS1 and its functional mechanisms in pancreatic cancer metastasis remain unknown, and the clinical significance of TP73-AS1 in human pancreatic cancer is also unclear. In the present study, the levels of TP73-AS1 and its candidate target miR-141 in pancreatic cancer and adjacent normal tissue were detected using qRT-PCR. The association between TP73-AS1 levels and the clinicopathologic characteristics of pancreatic cancer patients were analyzed. The relationship between TP73-AS1 and miR-141, and miR-141 and its candidate target 3-hydroxybutyrate dehydrogenase type 2 (BDH2) was confirmed using dual-luciferase reporter assays. TP73-AS1 and/or miR-141 were knocked down using siRNA or an inhibitor in pancreatic cancer cells and cell migration and invasion then examined. The results showed that TP73-AS1 was up-regulated in pancreatic cancer tissue and cell lines. High levels of TP73-AS1 were correlated with poor clinicopathological characteristics and shorter overall survival. MiR-141 was a direct target for TP73-AS1, while BDH2 was a direct target for miR-141. The knockdown of TP73-AS1 significantly inhibited the migration and invasion of pancreatic cancer cells, while the miR-141 inhibitor significantly restored the migration and invasion. Therefore, TP73-AS1 positively regulated BDH2 expression by sponging miR-141. These findings suggest that TP73-AS1 serves as an oncogene and promotes the metastasis of pancreatic cancer. Moreover, TP73-AS1 could serve as a predictor and a potential drug biotarget for pancreatic cancer.

Indexed as

Gene Expression Regulation, NeoplasticCell Line, TumorCell MovementFemaleHumansHydroxybutyrate DehydrogenaseKaplan-Meier EstimateMaleMicroRNAsMiddle AgedNeoplasm InvasivenessPancreatic NeoplasmsRNA InterferenceRNA, Long NoncodingUp-RegulationBDH2 protein, humanHydroxybutyrate Dehydrogenaselong non-coding RNA KIAA0495, humanMicroRNAsMIRN141 microRNA, humanRNA, Long NoncodingBDH2lncRNAmetastasismiR-141pancreatic cancerTP73-AS1

Identifiers

PMID30643007
PMCPMC6418400
OpenAlexW2908551240

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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.