Evidence map›Paper›PMID 34515325›Full record

ArticleInternational journal of oncology2021

Regulation of gliomagenesis and stemness through acid sensor ASIC1a.

Pendelton King, Jingwei Wan, Alyssa Aihui Guo, Shanchun Guo, Yugang Jiang, Mingli Liu

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Interaction of NF-κB and FOSL1 drives glioma stemness.Cellular and molecular life sciences : CMLS · 2024
    Article
  8. Review
  9. Article
  10. Ion Channels in Gliomas-From Molecular Basis to Treatment.International journal of molecular sciences · 2023
    Review
  11. Article
  12. 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

6 authors at 4 institutions in 2 countries.

Pendelton KingDepartment of Microbiology, Biochemistry and Immunology, Morehouse School of Medicine, Atlanta, GA 30310, USA.
Jingwei WanDepartment of Microbiology, Biochemistry and Immunology, Morehouse School of Medicine, Atlanta, GA 30310, USA.
Alyssa Aihui GuoDepartment of Biomedical Sciences, School of Medicine Greenville, University of South Carolina, Greenville, SC 29605, USA.
Shanchun GuoDepartment of Chemistry, Xavier University, New Orleans, LA 70125, USA.
Yugang JiangDepartment of Neurosurgery, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China.
Mingli LiuDepartment of Microbiology, Biochemistry and Immunology, Morehouse School of Medicine, Atlanta, GA 30310, USA.
Morehouse School of Medicine · USCentral South University · CNUniversity of South Carolina · USXavier University · US

Funding

TRPM7 induces tumorigenesis and stemness through Notch activation in gliomaSC1GM144021 · NIGMS · MOREHOUSE SCHOOL OF MEDICINE · PI LIU, MINGLI · 2022 to 2025
$1.4M
The Role of TRPM7 in Progression of Malignant GliomaSC3GM121230 · NIGMS · MOREHOUSE SCHOOL OF MEDICINE · PI LIU, MINGLI · 2018 to 2021
$426k
NIGMS NIH HHS SC1 GM144021NIGMS NIH HHS SC3 GM121230
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most prevalent and aggressive type of adult gliomas. Despite intensive therapy including surgery, radiation, and chemotherapy, invariable tumor recurrence occurs, which suggests that glioblastoma stem cells (GSCs) render these tumors persistent. Recently, the induction of GSC differentiation has emerged as an alternative method to treat GBM, and most of the current studies aim to convert GSCs to neurons by a combination of transcriptional factors. As the tumor microenvironment is typically acidic due to increased glycolysis and consequently leads to an increased production of lactic acid in tumor cells, in the present study, the role of acid‑sensing ion channel 1a (ASIC1a), an acid sensor, was explored as a tumor suppressor in gliomagenesis and stemness. The bioinformatics data from The Cancer Genome Atlas revealed that ASIC1 expression levels in GBM tumor tissues were lower than those in normal brain, and glioma patients with high ASIC1 expression had longer survival than those with low ASIC1 expression. Our immunohistochemistry data from tissue microarray revealed that ASIC1a expression was negatively associated with glioma grading. Functional studies revealed that the downregulation of ASIC1a promoted glioma cell proliferation and invasion, while upregulation of ASIC1a inhibited their proliferation and invasion. Furthermore, ASIC1a suppressed growth and proliferation of glioma cells through G1/S arrest and apoptosis induction. Mechanistically, ASIC1a negatively modulated glioma stemness via inhibition of the Notch signaling pathway and GSC markers CD133 and aldehyde dehydrogenase 1. ASIC1a is a tumor suppressor in gliomagenesis and stemness and may serve as a promising prognostic biomarker and target for GBM patients.

Indexed as

AC133 AntigenAcid Sensing Ion ChannelsAldehyde Dehydrogenase 1 FamilyApoptosisBrain NeoplasmsCell Line, TumorCell ProliferationGlioblastomaHumansNeoplasm InvasivenessNeoplastic Stem CellsTumor MicroenvironmentAC133 AntigenAcid Sensing Ion ChannelsAldehyde Dehydrogenase 1 FamilyASIC1 protein, humanPROM1 protein, humanaldehyde dehydrogenase 1ASIC1aCD133GSCsNotchtumor suppressor

Identifiers

PMID34515325
PMCPMC8448544
OpenAlexW3199502791

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.