Evidence map›Paper›PMID 17868871›Full record

ArticleMolecular immunology2008

Functional analysis of the host defense peptide Human Beta Defensin-1: new insight into its potential role in cancer.

Rebecca S Bullard, Willietta Gibson, Sudeep K Bose, Jamila K Belgrave, Andre C Eaddy, Corey J Wright, Debra J Hazen-Martin, Janice M Lage, Thomas E Keane, Tomas A Ganz and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecular immunology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 99 citations in OpenAlex.

  1. Review
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  7. Review
  8. Role of Defensins in Tumor Biology.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Review
  11. Structure, function, and evolution ofProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Review
  13. Article
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  15. Review
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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 at 3 institutions in 1 country.

Rebecca S BullardDepartment of Pathology and Laboratory Medicine, 165 Ashley Avenue, PO Box 250620, Charleston, SC 29425, USA.
Willietta Gibson
Sudeep K Bose
Jamila K Belgrave
Andre C Eaddy
Corey J Wright
Debra J Hazen-Martin
Janice M Lage
Thomas E Keane
Tomas A Ganz
Carlton D Donald
College of Charleston · USUniversity of California, Los Angeles · USMUSC Hollings Cancer Center · US

Funding

Functional Analysis of Beta-Defensin Loss of ExpressionK22CA096788 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI DONALD, CARLTON D · 2004 to 2006
$470k
RENOVATION TO SUPPORT SENSORY NEUROSCIENCE RESEARCHC06RR014516 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND, JOHN R · 1999 to 1999
–
NCI NIH HHS CA096788NCI NIH HHS K22 CA096788NCRR NIH HHS C06 RR014516NCRR NIH HHS C06RR14516
6 · The paper itself

Abstract

Although it is known that innate immunity is key for protecting the body against foreign agents such as bacteria, little is known about elements of the innate immune system that have anti-tumor activity. Human Beta Defensin-1 (hBD-1), an important component of the innate immune response, is lost at high frequencies in malignant prostatic tissue, while high levels of expression are maintained in adjacent benign regions. In prostate carcinoma, frequent genetic alterations occur in the 8p22-23 region and several studies indicate there may be multiple tumor suppressor genes present within this region. The high incidence of loss of hBD-1 expression in prostate cancer, along with its chromosomal location of 8p23.2, raised the possibility that it may play a role in tumor suppression. To gain insight as to its function in prostate cancer, hBD-1 was cloned and ectopically expressed in four prostate cancer cell lines. Induction of hBD-1 expression resulted in a decrease in cellular growth in DU145 and PC3 cells. However, hBD-1 has no effect on the growth of androgen receptor (AR) positive LNCaP prostate cancer cells, but was again growth suppressive to PC3 cells with ectopic AR expression (PC3/AR+). hBD-1 also caused rapid induction of cytolysis and caspase-mediated apoptosis in DU145 and PC3 prostate cancer cells. Although the regulation of hBD-1 was not addressed in this study, our preliminary data demonstrated that the pathways involved may include cMYC and PAX2. Data presented here are the first to provide evidence of its potential role in prostate cancer cell death.

Indexed as

Immunity, InnateApoptosisbeta-DefensinsCell DeathCell Line, TumorChromosome AberrationsChromosomes, Human, Pair 8Cloning, MolecularGene ExpressionGene Expression Regulation, NeoplasticHumansMalePAX2 Transcription FactorProstatic NeoplasmsProto-Oncogene Proteins c-mycTumor Suppressor Proteinsbeta-DefensinsDEFB1 protein, humanPAX2 protein, humanPAX2 Transcription FactorProto-Oncogene Proteins c-mycTumor Suppressor Proteins

Identifiers

PMID17868871
PMCPMC2131727
OpenAlexW2003255289

What OpenQuestion 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 OpenQuestion graph.