Evidence map›Paper›PMID 42769006›Full record

ArticleJournal of cellular and molecular medicine2026

Deciphering the Dysregulated Pathways and Candidate Therapeutic Compounds for Primary Ovarian Cancer Using Whole Transcriptomics Data and Next Generation Knowledge Discovery Strategies.

Peter Natesan Pushparaj, Kalamegam Gauthaman, Alaa G Alahmadi, Reem Nabil Hassan, Hind A Alkhatabi, Ammar Al-Farga

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Peter Natesan PushparajInstitute of Genomic Medicine Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID https://orcid.org/0000-0001-7574-1880
Kalamegam GauthamanCenter for Transdisciplinary Research, Department of Pharmacology, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Chennai, India.
Alaa G AlahmadiDepartment of Biological Science, College of Science, University of Jeddah, Jeddah, Saudi Arabia.ORCID https://orcid.org/0009-0009-0160-6745
Reem Nabil HassanDepartment of Biological Sciences, Faculty of Sciences-, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID https://orcid.org/0000-0002-4671-7053
Hind A AlkhatabiDepartment of Biological Science, College of Science, University of Jeddah, Jeddah, Saudi Arabia.ORCID https://orcid.org/0000-0002-8082-838X
Ammar Al-FargaDepartment of Biological Science, College of Science, University of Jeddah, Jeddah, Saudi Arabia.ORCID https://orcid.org/0000-0002-0233-5539

Funding

Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia 1045
6 · The paper itself

Abstract

Ovarian cancer (OC) is a type of gynaecological cancer with a higher mortality rate due to diagnosis at an advanced stage and limited treatment options. This study aimed to leverage transcriptomic data to identify cellular and molecular pathways and potential anti-cancer compounds that specifically target primary invasive epithelial ovarian cancer (EOC). By employing next-generation knowledge discovery (NGKD) methodologies, we sought to unravel the intricate molecular landscape of primary invasive EOC using RNA sequencing (RNA-seq) data and decipher potential therapeutics for this debilitating disease. We performed NGKD analysis of the Gene Expression Omnibus (GEO) dataset GSE1295399 obtained from whole RNA-seq experiments. Using the raw counts and filtered metadata from GEO, we identified 2123 differentially expressed genes (DEGs) based on a Log

Indexed as

Antineoplastic AgentsCarcinoma, Ovarian EpithelialDrug DiscoveryGene Expression ProfilingGene Expression Regulation, NeoplasticOvarian NeoplasmsTranscriptomeComputational BiologyFemaleGene OntologyGene Regulatory NetworksHumansSignal TransductionAntineoplastic AgentsExpressAnalystL1000CDS2L1000FWDovarian cancerprecision medicineRNAseqWebGestalt

Identifiers

PMID42769006
PMCPMC13595174

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.