Evidence map›Paper›PMID 32757096›Full record

ArticleHuman cell2020

MicroRNA-1469-5p promotes the invasion and proliferation of pancreatic cancer cells via direct regulating the NDRG1/NF-κB/E-cadherin axis.

Jinju Liu, Chaoyu Zhu, Lingzhi Zhang, Hongmei Lu, Zhen Wang, Jian Lv, Changru Fan

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 35% 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, 12 citations in OpenAlex.

  1. Review
  2. Unraveling the therapeutic landscape of miRNAs in pancreatic cancer.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  3. Review
  4. Article
  5. miRNAs in pancreatic cancer progression and metastasis.Clinical & experimental metastasis · 2024
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. 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

7 authors at 1 institution in 1 country.

Jinju LiuDepartment of Internal Medicine, Linyi Cancer Hospital, Linyi, Shandong, China.
Chaoyu ZhuDepartment of Abdominal Surgery, Linyi Cancer Hospital, Linyi, Shandong, China.
Lingzhi ZhangDepartment of Internal Medicine, Linyi Cancer Hospital, Linyi, Shandong, China.
Hongmei LuDepartment of Internal Medicine, Linyi Cancer Hospital, Linyi, Shandong, China.
Zhen WangDepartment of Internal Medicine, Linyi Cancer Hospital, Linyi, Shandong, China.
Jian LvDepartment of Internal Medicine, Linyi Cancer Hospital, Linyi, Shandong, China.
Changru FanDepartment of Abdominal Surgery, Linyi Cancer Hospital, Linyi, Shandong, China. fanchangru11@sina.com.
Linyi People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Numerous studies demonstrated that microRNAs (miRNAs) were highly involved in pancreatic cancer development. However, the functional roles of many miRNAs remain elusive in pancreatic cancer. In the present study, we analyzed previous published microarray data and found that miR-1469-5p was one of top upregulated miRNAs in pancreatic tumors. Our further study showed that miR-1469-5p was highly expressed in collected pancreatic tumors and its upregulation was associated with lymph node metastasis and tumors of advanced TNM stage. Functional analysis with miR-1469-5p inhibitor showed that downregulation of miR-1469-5p repressed pancreatic cancer cell proliferation and invasion. Mechanistically, miR-1469-5p directly interacted with metastasis suppressor NDRG1 mRNA and downregulated expression of NDRG1 to activate NF-κB pathway in pancreatic cancer cells. It was also found that miR-1469-5p decreased expression of E-cadherin, a metastasis related gene repressed by NF-κB pathway, in pancreatic cancer cells. Transfection of NDRG1 small interference RNA (siRNA) attenuated the function of miR-1469-5p inhibitor in pancreatic cancer cells. Moreover, miR-1469-5p expression was negatively associated with NDRG1 and E-cadherin mRNA levels in pancreatic tumors. Taken together, miR-1469-5p may exert its oncogenic potential in pancreatic cancer via regulating a NDRG1/NF-κB/E-cadherin axis, suggesting that it may be clinically valuable as a prognostic biomarker of pancreatic cancer.

Indexed as

Biomarkers, TumorCadherinsCell Cycle ProteinsCell Line, TumorCell ProliferationGene ExpressionGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsMicroRNAsNeoplasm InvasivenessNF-kappa BN-myc Downstream-Regulated Gene 1 ProteinPancreatic NeoplasmsPrognosisSignal TransductionBiomarkers, TumorCadherinsCell Cycle ProteinsIntracellular Signaling Peptides and ProteinsMicroRNAsNF-kappa BN-myc Downstream-Regulated Gene 1 ProteinmicroRNA-1469-5pNDRG1NF-κbPancreatic cancer

Identifiers

PMID32757096
OpenAlexW3048106061

What OpenQuestion holds

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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.