Evidence map›Paper›PMID 35657693›Full record

ArticleCancer science2022

Therapeutic advantage of targeting lysosomal membrane integrity supported by lysophagy in malignant glioma.

Yongwei Jing, Masahiko Kobayashi, Ha Thi Vu, Atsuko Kasahara, Xi Chen, Loc Thi Pham, Kenta Kurayoshi, Yuko Tadokoro, Masaya Ueno, Tomoki Todo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
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

12 authors at 2 institutions in 1 country.

Yongwei JingDivision of Molecular Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Masahiko KobayashiDivision of Molecular Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Ha Thi VuDivision of Molecular Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Atsuko KasaharaInstitute for Frontier Science Initiative, Kanazawa University, Kanazawa, Japan.
Xi ChenDivision of Molecular Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Loc Thi PhamDivision of Molecular Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Kenta KurayoshiDivision of Molecular Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Yuko TadokoroDivision of Molecular Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Masaya UenoDivision of Molecular Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Tomoki TodoDivision of Innovative Cancer Therapy, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Mitsutoshi NakadaDepartment of Neurosurgery, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.ORCID https://orcid.org/0000-0001-9419-6101
Atsushi HiraoDivision of Molecular Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.ORCID https://orcid.org/0000-0001-7818-8240
Kanazawa University · JPThe University of Tokyo · JP

Funding

Japan Agency for Medical Research and DevelopmentMinistry of Education, Culture, Sports, Science and Technology 19H01033Ministry of Education, Culture, Sports, Science and Technology 20K07566
6 · The paper itself

Abstract

Lysosomes function as the digestive system of a cell and are involved in macromolecular recycling, vesicle trafficking, metabolic reprogramming, and progrowth signaling. Although quality control of lysosome biogenesis is thought to be a potential target for cancer therapy, practical strategies have not been established. Here, we show that lysosomal membrane integrity supported by lysophagy, a selective autophagy for damaged lysosomes, is a promising therapeutic target for glioblastoma (GBM). In this study, we found that ifenprodil, an FDA-approved drug with neuromodulatory activities, efficiently inhibited spheroid formation of patient-derived GBM cells in a combination with autophagy inhibition. Ifenprodil increased intracellular Ca

Indexed as

GlioblastomaGliomaAutophagyChloroquineHumansLysosomesMacroautophagyChloroquineautophagycalciumglioblastomalysosomal membrane integritylysosomal membrane turnover

Identifiers

PMID35657693
PMCPMC9357661
OpenAlexW4281714258

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.