Evidence map›Paper›PMID 31013784›Full record

ArticleCancers2019

Transient Receptor Potential Mucolipin-1 Channels in Glioblastoma: Role in Patient's Survival.

Maria Beatrice Morelli, Consuelo Amantini, Daniele Tomassoni, Massimo Nabissi, Antonella Arcella, Giorgio Santoni

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. Article
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  11. Ion Channels in Gliomas-From Molecular Basis to Treatment.International journal of molecular sciences · 2023
    Review
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  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

6 authors at 2 institutions in 1 country.

Maria Beatrice MorelliSchool of Pharmacy, University of Camerino, 62032 Camerino, Italy. mariabeatrice.morelli@unicam.it.
Consuelo AmantiniSchool of Biosciences and Veterinary Medicine, University of Camerino, 62032 Camerino, Italy. consuelo.amantini@unicam.it.
Daniele TomassoniSchool of Biosciences and Veterinary Medicine, University of Camerino, 62032 Camerino, Italy. daniele.tomassoni@unicam.it.
Massimo NabissiSchool of Pharmacy, University of Camerino, 62032 Camerino, Italy. massimo.nabissi@unicam.it.ORCID 0000-0003-0165-1385
Antonella ArcellaIRCCS NEUROMED, 86077 Pozzilli, Italy. arcella@neuromed.it.
Giorgio SantoniSchool of Pharmacy, University of Camerino, 62032 Camerino, Italy. giorgio.santoni@unicam.it.
Università di Camerino · ITIstituto Neurologico Mediterraneo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A link between mucolipin channels and tumors has been recently suggested. Herein, we aim to investigate the transient receptor potential mucolipin (TRPML)-1 relevance in glioblastoma. The expression of this channel was evaluated via qRT-PCR and immunohistochemistry in biopsies from 66 glioblastoma patients and two human glioblastoma cell lines and compared to normal human brain, astrocytes, and epileptic tissues. The subcellular distribution of TRPML-1 was examined via confocal microscopy in the glioma cell lines. Then, to assess the role of TRPML-1, cell viability assays have been conducted in T98 and U251 cell lines treated with the specific TRPML-1 agonist, MK6-83. We found that MK6-83 reduced cell viability and induced caspase-3-dependent apoptosis. Indeed, the TRPML-1 silencing or the blockage of TRPML-1 dependent [Ca

Indexed as

autophagyglioblastomamucolipinsoverall survivalTRP channelTRPML-1

Identifiers

PMID31013784
PMCPMC6521337
OpenAlexW2936181313

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.