Evidence map›Paper›PMID 32667745›Full record

ArticleJournal of cellular and molecular medicine2020

Aberrant ASPM expression mediated by transcriptional regulation of FoxM1 promotes the progression of gliomas.

Wen-Jing Zeng, Quan Cheng, Zhi-Peng Wen, Jie-Ya Wang, Yan-Hong Chen, Jie Zhao, Zhi-Cheng Gong, Xiao-Ping Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. ASPM promotes ATR-CHK1 activation and stabilizes stalled replication forks in response to replication stress.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Article
  11. Transcription Factors with Targeting Potential in Gliomas.International journal of molecular sciences · 2022
    Review
  12. Article
  13. Pharmacogenomics and personalized medicine · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. A multi-mode Wnt- and stemness-regulatory module dictated by FOXM1 and ASPM isoform I in gastric cancer.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2021
    Article
  19. Article
  20. 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

8 authors at 1 institution in 1 country.

Wen-Jing ZengDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Quan ChengDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0003-2401-5349
Zhi-Peng WenDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Jie-Ya WangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Yan-Hong ChenDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Jie ZhaoNeurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Zhi-Cheng GongDepartment of Pharmacy, Xiangya Hospital, Central South University, Changsha, China.
Xiao-Ping ChenDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-2910-9152
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gliomas are the most common form of malignant tumour in the central nervous system. However, the molecular mechanism of the tumorigenesis and progression of gliomas remains unclear. In this study, we used the GEO database to identify genes differentially expressed in gliomas and predict the prognosis of glioma. We observed that ASPM mRNA was increased obviously in glioma tissue, and higher ASPM mRNA expression predicted worse disease prognosis. ASPM was highly expressed in glioma cell lines U87-MG and U251, and knockdown of ASPM expression in these cells significantly repressed the proliferation, migration and invasion ability and induced G0/G1 phase arrest. In addition, down-regulation of ASPM suppressed the growth of glioma in nude mice. Five potential binding sites for transcription factor FoxM1 were predicted in the ASPM promoter. FoxM1 overexpression significantly increased the expression of ASPM and promoted the proliferation and migration of glioma cells, which was abolished by ASPM ablation. ChIP and dual-luciferase reporter analysis confirmed that FoxM1 bound to the ASPM promoter at -236 to -230 bp and -1354 to -1348 bp and activated the transcription of ASPM directly. Collectively, our results demonstrated for the first time that aberrant ASPM expression mediated by transcriptional regulation of FoxM1 promotes the malignant properties of glioma cells.

Indexed as

AnimalsCarcinogenesisCell Line, TumorCell MovementCell ProliferationDisease ProgressionDown-RegulationFemaleForkhead Box Protein M1Gene Expression Regulation, NeoplasticGliomaHumansMiceMice, Inbred BALB CMice, NudeNerve Tissue ProteinsASPM protein, humanForkhead Box Protein M1FOXM1 protein, humanNerve Tissue ProteinsASPMbiomarkerFoxM1glioma

Identifiers

PMID32667745
PMCPMC7520292
OpenAlexW3043237104

What OpenQuestion holds

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LicenceCC BY
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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.