Evidence map›Paper›PMID 37644376›Full record

ArticleTranslational stroke research2024

Dysregulated Genes and Signaling Pathways in the Formation and Rupture of Intracranial Aneurysm.

Munish Kumar, Krishna Patel, Shobia Chinnapparaj, Tanavi Sharma, Ashish Aggarwal, Navneet Singla, Madhivanan Karthigeyan, Apinderpreet Singh, Sushanta Kumar Sahoo, Manjul Tripathi and 15 more

Abstract read
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Article in Translational stroke research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
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

25 authors at 2 institutions in 1 country.

Munish KumarDivision of Neuro-anesthesia, Department of Anesthesia and Intensive Care, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Krishna Patel *Institute of Bioinformatics, International Tech Park, Bangalore, India.
Shobia Chinnapparaj *Division of Neuro-anesthesia, Department of Anesthesia and Intensive Care, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Tanavi SharmaDivision of Neuro-anesthesia, Department of Anesthesia and Intensive Care, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Ashish AggarwalDepartment of Neurosurgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Navneet SinglaDepartment of Neurosurgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Madhivanan KarthigeyanDepartment of Neurosurgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Apinderpreet SinghDepartment of Neurosurgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Sushanta Kumar SahooDepartment of Neurosurgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Manjul TripathiDepartment of Neurosurgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Aastha TakkarDepartment of Neurology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Tulika GuptaDepartment of Anatomy, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Arnab PalDepartment of Biochemistry, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Savita Verma AttriPediatric Biochemistry, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Yogender Singh BansalDepartment of Forensic Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Radha Kanta RathoDepartment of Virology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Sunil K GuptaDepartment of Neurosurgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Madhu KhullarDepartment of Experimental Medicine and Biotechnology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Rakesh Kumar VashishtaDepartment of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Kanchan Kumar MukherjeeDepartment of Neurosurgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Vinod Kumar GroverDivision of Neuro-anesthesia, Department of Anesthesia and Intensive Care, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Rajendra PrasadDepartment of Biochemistry, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Aditi ChatterjeeInstitute of Bioinformatics, International Tech Park, Bangalore, India.
Harsha GowdaInstitute of Bioinformatics, International Tech Park, Bangalore, India.
Hemant BhagatDivision of Neuro-anesthesia, Department of Anesthesia and Intensive Care, Postgraduate Institute of Medical Education and Research, Chandigarh, India. bhagat.hemant@pgimer.edu.in.
Post Graduate Institute of Medical Education and Research · INInstitute of Bioinformatics · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intracranial aneurysm (IA) has the potential to rupture. Despite scientific advances, we are still not in a position to screen patients for IA and identify those at risk of rupture. It is critical to comprehend the molecular basis of disease to facilitate the development of novel diagnostic strategies. We used transcriptomics to identify the dysregulated genes and understand their role in the disease biology. In particular, RNA-Seq was performed in tissue samples of controls, unruptured IA, and ruptured IA. Dysregulated genes (DGs) were identified and analyzed to understand the functional aspects of molecules. Subsequently, candidate genes were validated at both transcript and protein level. There were 314 DGs in patients with unruptured IA when compared to control samples. Out of these, SPARC and OSM were validated as candidate molecules in unruptured IA. PI3K-AKT signaling pathway was found to be an important pathway for the formation of IA. Similarly, 301 DGs were identified in the samples of ruptured IA when compared with unruptured IAs. CTSL was found to be a key candidate molecule which along with Hippo signaling pathway may be involved in the rupture of IA. We conclude that activation of PI3K-AKT signaling pathway by OSM along with up-regulation of SPARC is important for the formation of IA. Further, regulation of Hippo pathway through PI3K-AKT signaling results in the down-regulation of YAP1 gene. This along with up-regulation of CTSL leads to further weakening of aneurysm wall and its subsequent rupture.

Indexed as

Aneurysm, RupturedIntracranial AneurysmSignal TransductionAdultAgedFemaleHippo Signaling PathwayHumansMaleMiddle AgedOsteonectinPhosphatidylinositol 3-KinasesOsteonectinPhosphatidylinositol 3-KinasesSPARC protein, humanCTSLIntracranial aneurysmOSMSignaling pathwaySPARCTranscriptome analysis

Identifiers

PMID37644376
OpenAlexW4386243550

What Socratic holds

Textmetadata
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.