Evidence map›Paper›PMID 35409086›Full record

ArticleInternational journal of molecular sciences2022

SOAT1: A Suitable Target for Therapy in High-Grade Astrocytic Glioma?

Mario Löhr, Wolfgang Härtig, Almut Schulze, Matthias Kroiß, Silviu Sbiera, Constantin Lapa, Bianca Mages, Sabrina Strobel, Jennifer Elisabeth Hundt, Simone Bohnert and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. [p53-SOAT1 Axis: A Novel Target for Tumor Lipid Metabolism and Therapy].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2025
    Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Cholesterol esterification and p53-mediated tumor suppression.Exploration of targeted anti-tumor therapy · 2023
    Article
  10. Review
  11. 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

13 authors at 8 institutions in 2 countries.

Mario LöhrDepartment of Neurosurgery, University Hospital Wuerzburg, 97080 Wuerzburg, Germany.
Wolfgang HärtigPaul Flechsig Institute for Brain Research, University of Leipzig, 04103 Leipzig, Germany.
Almut SchulzeDivision of Tumor Metabolism and Microenvironment, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Matthias KroißDepartment of Internal Medicine IV, University Hospital Munich, Ludwig-Maximilians-Universität Munich, 80336 Munich, Germany.
Silviu SbieraDepartment of Internal Medicine I, Division of Endocrinology and Diabetes, University Hospital, University of Wuerzburg, 97080 Wuerzburg, Germany.ORCID 0000-0002-6271-5533
Constantin LapaNuclear Medicine, Medical Faculty, University of Augsburg, 86156 Augsburg, Germany.ORCID 0000-0001-7536-2207
Bianca MagesInstitute for Anatomy, University of Leipzig, 04103 Leipzig, Germany.
Sabrina StrobelInstitute of Pathology, Department of Neuropathology, University of Wuerzburg, Josef-Schneider-Str. 2, 97080 Wuerzburg, Germany.
Jennifer Elisabeth HundtLuebeck Institute of Experimental Dermatology, University of Luebeck, 23538 Luebeck, Germany.
Simone BohnertInstitute of Forensic Medicine, University of Wuerzburg, 97080 Wuerzburg, Germany.
Stefan KircherInstitute of Pathology, Department of Neuropathology, University of Wuerzburg, Josef-Schneider-Str. 2, 97080 Wuerzburg, Germany.
Sudha Janaki-RamanDonald B. and Catherine C. Marron Cancer Metabolism Center, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Camelia-Maria MonoranuInstitute of Pathology, Department of Neuropathology, University of Wuerzburg, Josef-Schneider-Str. 2, 97080 Wuerzburg, Germany.
University of Würzburg · DELeipzig University · DEGerman Cancer Research Center · DELudwig-Maximilians-Universität München · DEMemorial Sloan Kettering Cancer Center · USUniversitätsklinikum Würzburg · DEUniversity of Augsburg · DEUniversity of Lübeck · DE

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Targeting molecular alterations as an effective treatment for isocitrate dehydrogenase-wildtype glioblastoma (GBM) patients has not yet been established. Sterol-O-Acyl Transferase 1 (SOAT1), a key enzyme in the conversion of endoplasmic reticulum cholesterol to esters for storage in lipid droplets (LD), serves as a target for the orphan drug mitotane to treat adrenocortical carcinoma. Inhibition of SOAT1 also suppresses GBM growth. Here, we refined SOAT1-expression in GBM and

Indexed as

Adrenal Cortex NeoplasmsAdrenocortical CarcinomaBrain NeoplasmsGlioblastomaGliomaHumansIsocitrate DehydrogenaseMutationSterol O-AcyltransferaseIsocitrate DehydrogenaseSterol O-Acyltransferasesterol O-acyltransferase 1astrocytomaglioblastomaIDH1/2lipid dropletsmitotaneSOAT1targeted therapy

Identifiers

PMID35409086
PMCPMC8998855
OpenAlexW4221073088

What Socratic 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 Socratic graph.