Evidence map›Paper›PMID 39568072›Full record

ReviewMolecular brain2024

Sonic hedgehog signalling pathway in CNS tumours: its role and therapeutic implications.

Andrew Awuah Wireko, Adam Ben-Jaafar, Jonathan Sing Huk Kong, Krishitha Meenu Mannan, Vivek Sanker, Sophie-Liliane Rosenke, Allswell Naa Adjeley Boye, Princess Afia Nkrumah-Boateng, Jeisun Poornaselvan, Muhammad Hamza Shah and 2 more

Abstract readReview
In one paragraph

Review in Molecular brain, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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.

Andrew Awuah WirekoFaculty of Medicine, Sumy State University, Sumy, 40007, Ukraine. andyvans36@yahoo.com.ORCID 0000-0003-2380-2949
Adam Ben-JaafarSchool of Medicine, University College Dublin, Belfield, Dublin 4, Ireland.
Jonathan Sing Huk KongSchool of Medicine, College of Medical & Veterinary Life Sciences, University of Glasgow, Glasgow, UK.
Krishitha Meenu MannanSchool of Medicine, Dentistry & Biomedical Sciences, Queen's University Belfast, Belfast, UK.
Vivek SankerDepartment of Neurosurgery, Stanford University, Stanford, CA, USA.
Sophie-Liliane RosenkeSchool of Medicine, Lancaster University, Lancaster, UK.
Allswell Naa Adjeley BoyeUniversity of Ghana Medical School, Accra, Ghana.
Princess Afia Nkrumah-BoatengUniversity of Ghana Medical School, Accra, Ghana.
Jeisun PoornaselvanSchool of Medicine, University College Dublin, Belfield, Dublin 4, Ireland.
Muhammad Hamza ShahSchool of Medicine, Dentistry & Biomedical Sciences, Queen's University Belfast, Belfast, UK.
Toufik Abdul-RahmanFaculty of Medicine, Sumy State University, Sumy, 40007, Ukraine.
Oday AtallahDepartment of Neurosurgery, Hannover Medical School, Carl-Neuberg-Strasse 1, 30625, Hannover, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CNS tumours encompass a diverse group of neoplasms with significant morbidity and mortality. The SHH signalling pathway plays a critical role in the pathogenesis of several CNS tumours, including gliomas, medulloblastomas and others. By influencing cellular proliferation, differentiation and migration in CNS tumours, the SHH pathway has emerged as a promising target for therapeutic intervention. Current strategies such as vismodegib and sonidegib have shown efficacy in targeting SHH pathway activation. However, challenges such as resistance mechanisms and paradoxical effects observed in clinical settings underscore the complexity of effectively targeting this pathway. Advances in gene editing technologies, particularly CRISPR/Cas9, have provided valuable tools for studying SHH pathway biology, validating therapeutic targets and exploring novel treatment modalities. These innovations have paved the way for a better understanding of pathway dynamics and the development of more precise therapeutic interventions. In addition, the identification and validation of biomarkers of SHH pathway activation are critical to guide clinical decision making and improve patient outcomes. Molecular profiling and biomarker discovery efforts are critical steps towards personalised medicine approaches in the treatment of SHH pathway-associated CNS tumours. While significant progress has been made in understanding the role of the SHH pathway in CNS tumorigenesis, ongoing research is essential to overcome current therapeutic challenges and refine treatment strategies. The integration of molecular insights with advanced technologies and clinical expertise holds great promise for developing more effective and personalised therapies for patients with SHH pathway-driven CNS tumours.

Indexed as

Central Nervous System NeoplasmsHedgehog ProteinsSignal TransductionAnimalsHumansHedgehog ProteinsBrain tumoursMolecular neuro-oncologyNeuro-geneticsSonic Hedgehog signalling pathway

Identifiers

PMID39568072
PMCPMC11580395

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Registered trials

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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.