Evidence map›Paper›PMID 29302888›Full record

ArticleJournal of neuro-oncology2018

Overexpression of aryl hydrocarbon receptor (AHR) signalling pathway in human meningioma.

Noble Kumar Talari, Manas K Panigrahi, Sailaja Madigubba, Prakash Babu Phanithi

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neuro-oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  5. Review
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  7. Article
  8. AhR and HIF-1International journal of cell biology · 2023
    Article
  9. Review
  10. Article
  11. Review
  12. AhR and Cancer: From Gene Profiling to Targeted Therapy.International journal of molecular sciences · 2021
    Review
  13. Article
  14. Article
  15. The Role of Aryl Hydrocarbon Receptor (AhR) in Brain Tumors.International journal of molecular sciences · 2020
    Review
  16. Article
  17. Review
  18. Article
  19. 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

4 authors at 2 institutions in 1 country.

Noble Kumar TalariDepartment of Biotechnology & Bioinformatics, School of Life Sciences, University of Hyderabad, Hyderabad, TS, 500046, India.
Manas K PanigrahiDepartment of Neurosurgery, KIMS, Secunderabad, India.
Sailaja MadigubbaDepartment of Neurosurgery, KIMS, Secunderabad, India.
Prakash Babu PhanithiDepartment of Biotechnology & Bioinformatics, School of Life Sciences, University of Hyderabad, Hyderabad, TS, 500046, India. prakash@uohyd.ac.in.ORCID http://orcid.org/0000-0002-1528-8575
Krishna Institute of Medical Sciences · INUniversity of Hyderabad · IN

Funding

Department of Biotechnology, Ministry of Science and Technology BT/PR18168/MED/29/1064/2016Department of Biotechnology, Ministry of Science and Technology (IN) BT/PR13111/MED/29/149/2009 dated 24-06-2010Department of Science and Technology, Government of India SB/EMEQ-257/2013 dated 12-07-2013Department of Science and Technology, Government of India SR/CSRI/196/2016University Grants Commission (INDIA) UH/UPE-2/28/2015
6 · The paper itself

Abstract

Aryl hydrocarbon receptor (AHR) is a ligand activated transcription factor and involved in tumorigenesis of many cancers. However there are no reports on AHR in human meningioma. Therefore we examined the status of the AHR and its signalling molecules in human meningioma by using tumor biopsy samples and autopsy control meninges. We report the up regulation of AHR pathway genes like aryl hydrocarbon receptor nuclear translocator (ARNT), aldehyde dehydrogenase1family memberA3 (ALDH1A3), cytochrome P450, family1, subfamily A polypeptide1 (CYP1A1) and TCCD induced poly ADP ribose polymerase (TIPARP) gene expression in human meningioma. Further, AHR protein expression was found to be up regulated in all grades of human meningioma. We found that AHR localized in the nucleus for high grade anaplastic meningioma through immunohistochemical analysis. Since AHR signalling pathway was known to involve in inhibition of apoptosis in cancer cells, we evaluated the cyclophilin D levels which maintains mitochondrial permeability transition pore a critical event during apoptosis. We report that cyclophilin D levels were upregulated in all grades of human meningioma compared to control meninges. Finally we also evaluated c-Fos protein levels as its levels were regulated by AHR. Here we report that c-Fos protein levels were down regulated in all grades of human meningioma compared to control meninges. To sum-up we found that AHR signalling pathway components were upregulated, as the grade of the meningioma progresses from low to high grade, suggesting an important role of AHR signalling pathway in human meningioma.

Indexed as

Basic Helix-Loop-Helix ProteinsCyclophilinsGene Expression Regulation, NeoplasticHumansMeningeal NeoplasmsMeningesMeningiomaNeoplasm GradingPeptidyl-Prolyl Isomerase DProto-Oncogene Proteins c-fosReceptors, Aryl HydrocarbonRNA, MessengerSignal TransductionAHR protein, humanBasic Helix-Loop-Helix ProteinsCyclophilinsPeptidyl-Prolyl Isomerase DPPID protein, humanProto-Oncogene Proteins c-fosReceptors, Aryl HydrocarbonRNA, MessengerAryl hydrocarbon receptor (AHR)Human meningiomaIndoleamine 2, 3 dioxygenases (IDO)Kynurenine (KYN)

Identifiers

PMID29302888
OpenAlexW2781573989

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.