Evidence map›Paper›PMID 39630373›Full record

ArticleBiochemical genetics2025

Prevalence of SPOP and IDH Gene Mutations in Prostate Cancer in a Jordanian Population.

Mohammed S Alorjani, Samir Al Bashir, Basmah Al-Zaareer, Sohaib Al-Khatib, Raed M Al-Zoubi, Bahaa Al-Trad, Manal AbuAlarja, Ayman Alzu'bi, Mohammad Al-Hamad, Khalid Al-Batayneh and 1 more

Abstract read
In one paragraph

Article in Biochemical genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Mohammed S AlorjaniDepartment of Pathology and Microbiology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.
Samir Al BashirDepartment of Pathology and Microbiology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.
Basmah Al-ZaareerDepartment of Biological Sciences, Faculty of Science, Yarmouk University, Irbid, 21163, Jordan.
Sohaib Al-KhatibDepartment of Pathology and Microbiology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.
Raed M Al-ZoubiSurgical Research Section, Department of Surgery, Hamad Medical Corporation, Doha, Qatar. ralzoubi@hamad.qa.ORCID http://orcid.org/0000-0002-0548-429X
Bahaa Al-TradDepartment of Biological Sciences, Faculty of Science, Yarmouk University, Irbid, 21163, Jordan.
Manal AbuAlarjaDepartment of Basic Medical Sciences, Faculty of Medicine, Yarmouk University, Irbid, 21163, Jordan.
Ayman Alzu'biDepartment of Basic Medical Sciences, Faculty of Medicine, Yarmouk University, Irbid, 21163, Jordan.
Mohammad Al-HamadDepartment of Pathology, College of Medicine, Imam Abdulrahman Bin Faisal University (IAU), Dammam, Saudi Arabia.
Khalid Al-BataynehDepartment of Biological Sciences, Faculty of Science, Yarmouk University, Irbid, 21163, Jordan.
Mazhar S Al-ZoubiDepartment of Basic Medical Sciences, Faculty of Medicine, Yarmouk University, Irbid, 21163, Jordan.

Funding

Deanship of Scientific Research and Graduate Studies at Yarmouk University 12/2020
6 · The paper itself

Abstract

Speckle-type POZ (SPOP) is described as an essential tumor suppressor factor in gastric cancer, colorectal cancer, and prostate cancer (PCa). SPOP gene mutations were reported in primary human PCa. Isocitrate dehydrogenase-1 (IDH1) oncogene mutations were detected in gliomas, acute myeloid leukemia, some benign and malignant cartilaginous tumors, and only 1% of PCa. This study aimed to investigate the prevalence of mutations of SPOP and IDH1 genes in PCa in the Jordanian population. One hundred formalin-fixed paraffin-embedded tissue samples were collected from patients diagnosed with prostate adenocarcinoma. The obtained specimens were subjected to genomic DNA extraction, PCR amplification, and direct sequencing of exons 4, 5, 6, and 7 of the SPOP gene and exon 6 of the IDH1 gene. SPOP gene mutations were found in 17% of PCa cases, while no mutation was detected in the screened exon 6 of the IDH1 gene. Clinicopathological data demonstrated a strong correlation between prostate-specific antigen (PSA) levels and both Gleason score (GS) and the International Society of Urological Pathology (ISUP) grade group (GG). There was no significant correlation between PSA levels and age (p = 0.816) nor there were significant associations for SPOP mutational status with age (p = 0.659), PSA levels (p = 0.395), GS (p = 0.259), and ISUP GG (p = 0.424) in the tested population. The study found a strong correlation between PSA levels and both GS and ISUP GG. It also identified a high frequency (17%) of SPOP gene mutations in Jordanian Arab PCa patients, mainly in exon 7. No IDH1 mutations were detected in exon 6.

Indexed as

Isocitrate DehydrogenaseMutationNuclear ProteinsProstatic NeoplasmsRepressor ProteinsAdultAgedAged, 80 and overHumansJordanMaleMiddle AgedPrevalenceIDH1 protein, humanIsocitrate DehydrogenaseNuclear ProteinsRepressor ProteinsSPOP protein, humanGenetic mutationIDH1Prostate cancerSPOP

Identifiers

PMID39630373
PMCPMC12602551

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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.