Evidence map›Paper›PMID 38672496›Full record

ReviewBiomolecules2024

Mechanism of Notch Signaling Pathway in Malignant Progression of Glioblastoma and Targeted Therapy.

Shenghao Wang, Sikuan Gu, Junfan Chen, Zhiqiang Yuan, Ping Liang, Hongjuan Cui

Abstract readReview
In one paragraph

Review in Biomolecules, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Nano-Based Technology in Glioblastoma.Molecules (Basel, Switzerland) · 2025
    Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. 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.

Shenghao WangCancer Center, Medical Research Institute, Southwest University, Chongqing 400716, China.
Sikuan GuState Key Laboratory of Resource Insects, Southwest University, Chongqing 400716, China.
Junfan ChenState Key Laboratory of Resource Insects, Southwest University, Chongqing 400716, China.
Zhiqiang YuanState Key Laboratory of Resource Insects, Southwest University, Chongqing 400716, China.
Ping LiangDepartment of Neurosurgery, Children's Hospital of Chongqing Medical University, Chongqing 400014, China.
Hongjuan CuiCancer Center, Medical Research Institute, Southwest University, Chongqing 400716, China.ORCID 0000-0003-1178-1570

Funding

Natural Science Foundation of Chongqing cstc2022ycjh-bgzxm0145The pilot program of Southwest University SWU-XDZD22006
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most aggressive form of glioma and the most common primary tumor of the central nervous system. Despite significant advances in clinical management strategies and diagnostic techniques for GBM in recent years, it remains a fatal disease. The current standard of care includes surgery, radiation, and chemotherapy, but the five-year survival rate for patients is less than 5%. The search for a more precise diagnosis and earlier intervention remains a critical and urgent challenge in clinical practice. The Notch signaling pathway is a critical signaling system that has been extensively studied in the malignant progression of glioblastoma. This highly conserved signaling cascade is central to a variety of biological processes, including growth, proliferation, self-renewal, migration, apoptosis, and metabolism. In GBM, accumulating data suggest that the Notch signaling pathway is hyperactive and contributes to GBM initiation, progression, and treatment resistance. This review summarizes the biological functions and molecular mechanisms of the Notch signaling pathway in GBM, as well as some clinical advances targeting the Notch signaling pathway in cancer and glioblastoma, highlighting its potential as a focus for novel therapeutic strategies.

Indexed as

GlioblastomaReceptors, NotchSignal TransductionAnimalsBrain NeoplasmsDisease ProgressionHumansMolecular Targeted TherapyReceptors, Notchbiological functionsclinicalglioblastomamolecular mechanismsNotch

Identifiers

PMID38672496
PMCPMC11048644

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.