Evidence map›Paper›PMID 28712306›Full record

ReviewExpert opinion on drug discovery2017

Targeting intrinsic apoptosis and other forms of cell death by BH3-mimetics in glioblastoma.

Georg Karpel-Massler, Chiaki Tsuge Ishida, Yiru Zhang, Marc-Eric Halatsch, M-Andrew Westhoff, Markus D Siegelin

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on drug discovery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Super-enhancers complexes zoom in transcription in cancer.Journal of experimental & clinical cancer research : CR · 2023
    Review
  10. Review
  11. Article
  12. Methodological Approaches for Assessing Metabolomic Changes in Glioblastomas.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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 2 institutions in 2 countries.

Georg Karpel-Masslera Department of Neurosurgery , Ulm University Medical Center , Ulm , Germany.
Chiaki Tsuge Ishidab Department of Pathology & Cell Biology , Columbia University Medical Center , New York , NY , USA.
Yiru Zhangb Department of Pathology & Cell Biology , Columbia University Medical Center , New York , NY , USA.
Marc-Eric Halatscha Department of Neurosurgery , Ulm University Medical Center , Ulm , Germany.
M-Andrew Westhoffc Department of Pediatrics and Adolescent medicine , Ulm University Medical Center , Ulm , Germany.
Markus D Siegelinb Department of Pathology & Cell Biology , Columbia University Medical Center , New York , NY , USA.
Columbia University Irving Medical Center · USUniversität Ulm · DE

Funding

Targeting Mutant IDH1 for a Novel Synthetic Lethal Interaction in Malignant GliomasR01NS102366 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SIEGELIN, MARKUS D · 2018 to 2022
$1.8M
Dual Inhibition of Mitochondrial Matrix Chaperones and Anti-Apoptotic Bcl-2 Family Members for Glioblastoma Therapy.R01NS095848 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SIEGELIN, MARKUS D · 2016 to 2020
$1.8M
Overcoming apoptotic resistance in glioblastoma by CP-d/n-ATF5, a novel tumor speK08NS083732 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SIEGELIN, MARKUS D · 2014 to 2018
$938k
NINDS NIH HHS K08 NS083732NINDS NIH HHS R01 NS095848NINDS NIH HHS R01 NS102366
6 · The paper itself

Abstract

introductionNovel approaches to treat malignant brain tumors are necessary since these neoplasms still display an unfavorable prognosis. Areas covered: In this review, the authors summarize and analyze recent preclinical data that suggest that targeting intrinsic apoptosis may be a suitable strategy for the treatment of malignant gliomas. They focus on the anti-apoptotic Bcl-2 family members of proteins and the recent drug developments in that field with a special focus on BH3-mimetics. With the discovery of BH3-mimetics that interfere with anti-apoptotic Bcl-2 family members in the low nanomolar range significant excitement has been generated towards these class of inhibitors, such as ABT-737, ABT-263 and the most recent successor, ABT-199 which is most advanced with respect to clinical application. The authors discuss the more recent selective inhibitors of Bcl-xL and Mcl-1. Concerning Mcl-1, these novel classes of inhibitors have the potential to impact malignant gliomas since these tumors reveal increased levels of Mcl-1. Expert opinion: The recent development of certain small molecules raises significant hope that intrinsic apoptosis might soon be efficiently targetable for malignancies of the central nervous system. That being said, additional studies are necessary to determine which of the BH3-mimetics might be most suitable.

Indexed as

AnimalsAntineoplastic AgentsApoptosisBiomimetic MaterialsBrain NeoplasmsCell DeathDrug DesignGlioblastomaHumansMolecular Targeted TherapyPeptide FragmentsProto-Oncogene ProteinsAntineoplastic AgentsBax protein (53-86)Peptide FragmentsProto-Oncogene ProteinsABT263ABT737apoptosisautophagyBH3-mimeticsMcl-1

Identifiers

PMID28712306
PMCPMC6143391
OpenAlexW2735113611

What OpenQuestion holds

Textmetadata
LicenceTDM
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.