Evidence map›Paper›PMID 29736210›Full record

ArticleAmerican journal of translational research2018

MiR-101 inhibits the proliferation and metastasis of lung cancer by targeting zinc finger E-box binding homeobox 1.

Le Han, Wenjuan Chen, Yanmin Xia, Yangrong Song, Zheng Zhao, Hao Cheng, Tao Jiang

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.3field-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

33 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Exosomal microRNA as a key regulator of PI3K/AKT pathways in human tumors.Medical oncology (Northwood, London, England) · 2024
    Review
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  9. MicroRNA 101 Attenuated NSCLC Proliferation through IDH2/HIFOxidative medicine and cellular longevity · 2022
    Article
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  11. Review
  12. Review
  13. Article
  14. 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.

Le HanDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, Shaanxi, China.
Wenjuan ChenDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, Shaanxi, China.
Yanmin XiaDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, Shaanxi, China.
Yangrong SongDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, Shaanxi, China.
Zheng ZhaoDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, Shaanxi, China.
Hao ChengDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, Shaanxi, China.
Tao JiangDepartment of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University Xi'an 710038, Shaanxi, China.
Air Force Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are involved in the development and progression of lung cancer. MicroRNA-101 (miR-101) displays crucial properties in non-small cell lung cancer (NSCLC) by negatively regulating cell proliferation and invasion, but the underlying molecular mechanisms remain largely unknown. In this study, we found that miR-101 was underexpressed while zinc finger E-box binding homeobox 1 (ZEB1) was highly upregulated in NSCLC tissues and cells. The downregulation of miR-101 was positively associated with lymph node metastasis and poor prognosis of NSCLC patients. Dual-luciferase reporter assay showed that miR-101 directly targeted ZEB1 in NSCLC cells. Enforced expression of miR-101 significantly inhibited NSCLC cell proliferation, apoptosis resistance, migration, and invasion in vitro, which were attenuated by ZEB1 overexpression and phenocopied by ZEB1 knockdown, respectively. Consistently, miR-101 retarded NSCLC growth and metastasis in vivo. The findings indicated that miR-101 suppressed NSCLC growth and metastasis by targeting ZEB1, thereby providing new evidence of miR-101 as a potential therapeutic target for NSCLC patients.

Indexed as

lung cancermetastasisMicroRNA-101proliferationzinc finger E-box binding homeobox 1

Identifiers

PMID29736210
PMCPMC5934576
OpenAlexW2954280010

What OpenQuestion holds

Textmetadata
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.