Evidence map›Paper›PMID 27183959›Full record

ArticleScientific reports2016

Species-specific mutual regulation of p53 and miR-138 between human, rat and mouse.

Jie Li, Wei Xia, Xueting Su, Xingliang Qin, Ying Chen, Shaohua Li, Jie Dong, Hongmei Ding, Hui Li, Aixue Huang and 12 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Pivotal role of microRNA-138 in human cancers.American journal of cancer research · 2019
    Review
  6. Article
  7. 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

22 authors at 3 institutions in 1 country.

Jie LiDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Wei XiaDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Xueting SuDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Xingliang QinDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Ying ChenDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Shaohua LiDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Jie DongDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Hongmei DingDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Hui LiDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Aixue HuangDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Xingfeng GeDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Lvbin HouDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Chaonan WangDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Leqiao SunDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Chenjun BaiDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Xuelian ShenDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Tao FangDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Yuanlin LiuDepartment of Cell Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Yi ZhangDepartment of Cell Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Hongru ZhangOtorhinolaryngological department, Haidian Section of Peking University third Hospital, Beijing 100080, China.
Hongwen ZhangDepartment of Interventional Radiology, General Hospital of Fuzhou, Fuzhou, China.
Ningsheng ShaoDepartment of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Beijing 100850, China.
Institute of Basic Medical Sciences of the Chinese Academy of Medical SciencesFuzhou General Hospital of Nanjing Military Command · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, p53 was identified to regulate the expression of many miRNAs and was also regulated by miRNAs. In this paper, we found that miR-138 showed a pronounced increase after p53 activation in human non-small cell lung cancer (NSCLC) cells, which is mediated by p53 binding sites in the promoter region of its host gene, but this did not happen with rat and mouse cells. More interestingly, we found that p53 could be also regulated by miR-138 in mouse and rat cells, but not in the human NSCLC cells. Our results suggest the existence of species-specific differences of the regulations of miRNA against its targets and the regulations of miRNA itself by other proteins.

Indexed as

Gene Expression RegulationAnimalsCell LineHumansMiceMicroRNAsRatsTumor Suppressor Protein p53MicroRNAsMIRN138 microRNA, humanMIRN138 microRNA, mouseMIRN138 microRNA, ratTumor Suppressor Protein p53

Identifiers

PMID27183959
PMCPMC4869026
OpenAlexW2404123824

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.