Evidence map›Paper›PMID 26038828›Full record

Trial reportPloS one2015

Expression and new exon mutations of the human Beta defensins and their association on colon cancer development.

Abdelhabib Semlali, Abdullah Al Amri, Arezki Azzi, Omair Al Shahrani, Maha Arafah, Muhammad Kohailan, Abdulrahman M Aljebreen, Othman Alharbi, Majid A Almadi, Nahla Ali Azzam and 3 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Pioneering Clinical Investigation: Beta Defensin Expression in Patients of Squamous Cell Carcinoma of Oral Cavity as a Forward-Looking Validation for Molecular Treatment.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 2025
    Article
  5. Review
  6. Role of Defensins in Tumor Biology.International journal of molecular sciences · 2023
    Review
  7. Improving Fmoc Solid Phase Synthesis of Human Beta Defensin 3.International journal of molecular sciences · 2022
    Article
  8. Article
  9. Review
  10. Article
  11. Antitumor effect of copper nanoparticles on human breast and colon malignancies.Environmental science and pollution research international · 2021
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Effects of Hexane Root Extract ofBioMed research international · 2019
    Article
  17. Review
  18. Enediyne-activated, EGFR-targeted human β-defensin 1 has therapeutic efficacy against non-small cell lung carcinoma.Laboratory investigation; a journal of technical methods and pathology · 2018
    Article
  19. Article
  20. 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

13 authors at 3 institutions in 2 countries.

Abdelhabib SemlaliGenome Research Chair, Department of Biochemistry, College of Science King Saud University, Riyadh, Kingdom of Saudi Arabia.
Abdullah Al AmriGenome Research Chair, Department of Biochemistry, College of Science King Saud University, Riyadh, Kingdom of Saudi Arabia.
Arezki AzziCollege of Medicine, Al Imam Muhammad Ibn Saud Islamic University (IMSIU), Riyadh, Kingdom of Saudi Arabia.
Omair Al ShahraniGenome Research Chair, Department of Biochemistry, College of Science King Saud University, Riyadh, Kingdom of Saudi Arabia.
Maha ArafahCollege of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Muhammad KohailanGenome Research Chair, Department of Biochemistry, College of Science King Saud University, Riyadh, Kingdom of Saudi Arabia.
Abdulrahman M AljebreenCollege of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia; Division of Gastroenterology, King Khalid University Hospital, King Saud University, Riyadh, Saudi Arabia.
Othman AlharbiCollege of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia; Division of Gastroenterology, King Khalid University Hospital, King Saud University, Riyadh, Saudi Arabia.
Majid A AlmadiDivision of Gastroenterology, King Khalid University Hospital, King Saud University, Riyadh, Saudi Arabia; Division of Gastroenterology, The McGill University Health Center, Montreal General Hospital, McGill University, Montreal, Canada.
Nahla Ali AzzamCollege of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia; Division of Gastroenterology, King Khalid University Hospital, King Saud University, Riyadh, Saudi Arabia.
Narasimha Reddy ParineGenome Research Chair, Department of Biochemistry, College of Science King Saud University, Riyadh, Kingdom of Saudi Arabia.
Mahmoud RouabhiaGroupe de Recherche en Écologie Buccale, Département de stomatologie, Faculté de Médecine Dentaire, Université Laval, Québec, Québec, Canada.
Mohammad S AlanaziGenome Research Chair, Department of Biochemistry, College of Science King Saud University, Riyadh, Kingdom of Saudi Arabia.
King Saud University · SAImam Mohammad ibn Saud Islamic University · SAUniversité Laval · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of cancer involves genetic predisposition and a variety of environmental exposures. Genome-wide linkage analyses provide evidence for the significant linkage of many diseases to susceptibility loci on chromosome 8p23, the location of the human defensin gene cluster. Human β-defensins (hBDs) are important molecules of innate immunity. This study was designed to analyze the expression and genetic variations in hBDs (hBD-1, hBD-2, hBD-3 and hBD-4) and their putative association with colon cancer. hBD gene expression and relative protein expression were evaluated by Real-Time polymerase chain reaction (qPCR) and immunohistochemistry, respectively, from 40 normal patients and 40 age-matched patients with colon cancer in Saudi Arabia. In addition, hBD polymorphisms were genotyped by exon sequencing and by promoter methylation. hBD-1, hBD-2, hBD-3 and hBD-4 basal messenger RNA expression was significantly lower in tumor tissues compared with normal tissues. Several insertion mutations were detected in different exons of the analyzed hBDs. However, no methylation in any hBDs promoters was detected because of the limited number of CpG islands in these regions. We demonstrated for the first time a link between hBD expression and colon cancer. This suggests that there is a significant link between innate immunity deregulation through disruption of cationic peptides (hBDs) and the potential development of colon cancer.

Indexed as

beta-DefensinsColonic NeoplasmsExonsGene Expression Regulation, NeoplasticMutationNeoplasm ProteinsAgedFemaleHumansMaleMiddle AgedPromoter Regions, GeneticReal-Time Polymerase Chain ReactionRNA, MessengerRNA, Neoplasmbeta-DefensinsNeoplasm ProteinsRNA, MessengerRNA, Neoplasm

Identifiers

PMID26038828
PMCPMC4454434
OpenAlexW1517881884

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.