Evidence map›Paper›PMID 24070418›Full record

ArticleThe American journal of pathology2013

Deletion of the olfactomedin 4 gene is associated with progression of human prostate cancer.

Hongzhen Li, Jaime Rodriguez-Canales, Wenli Liu, Jianqiong Zhu, Jeffrey C Hanson, Svetlana Pack, Zhengping Zhuang, Michael R Emmert-Buck, Griffin P Rodgers

Open access · hybridAbstract read
In one paragraph

Article in The American journal of pathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Olfactomedin 4 in cancer development and progression.Biochimica et biophysica acta. Reviews on cancer · 2025
    Review
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  14. Retinoid Chemoprevention: Who Can Benefit?Current pharmacology reports · 2015
    Article
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  18. 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

9 authors at 4 institutions in 1 country.

Hongzhen LiMolecular and Clinical Hematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland.
Jaime Rodriguez-Canales
Wenli Liu
Jianqiong Zhu
Jeffrey C Hanson
Svetlana Pack
Zhengping Zhuang
Michael R Emmert-Buck
Griffin P Rodgers
National Institutes of Health · USCenter for Cancer Research · USNational Heart Lung and Blood Institute · USNational Institute of Neurological Disorders and Stroke · US

Funding

Olfactomedin 4 Suppresses Prostate Cancer Cell Growth and Metastasis via NegativZIAHL006003 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI RODGERS, GRIFFIN · 2009 to 2025
$9.4M
Development of FISH Molecular Diagnostics to support Clinical Trials at NCIZIDBC011349 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PACK, SVETLANA · 2010 to 2014
$2.7M
Intramural NIH HHS
6 · The paper itself

Abstract

The olfactomedin 4 (OLFM4) gene is located on chromosome 13q14.3, which frequently is deleted in human prostate cancer. However, direct genetic evidence of OLFM4 gene alteration in human prostate cancer has not yet been obtained. In this study, we investigated the genetics, protein expression, and functions of the OLFM4 gene in human prostate cancer. We found overall 25% deletions within the OLFM4 gene in cancerous epithelial cells compared with adjacent normal epithelial cells that were microdissected from 31 prostate cancer specimens using laser-capture microdissection and genomic DNA sequencing. We found 28% to 45% hemizygous and 15% to 57% homozygous deletions of the OLFM4 gene via fluorescence in situ hybridization analysis from 44 different prostate cancer patient samples. Moreover, homozygous deletion of the OLFM4 gene significantly correlated with advanced prostate cancer. By using immunohistochemical analysis of 162 prostate cancer tissue array samples representing a range of Gleason scores, we found that OLFM4 protein expression correlated inversely with advanced prostate cancer, consistent with the genetic results. We also showed that a truncated mutant of OLFM4 that lacks the olfactomedin domain eliminated suppression of PC-3 prostate cancer cell growth. Together, our findings indicate that OLFM4 is a novel candidate tumor-suppressor gene for chromosome 13q and may shed new light on strategies that could be used for the diagnosis, prognosis, and treatment of prostate cancer patients.

Indexed as

Disease ProgressionGene DeletionAutophagyBase SequenceCathepsin DCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticGenome, HumanGranulocyte Colony-Stimulating FactorHomozygoteHumansIn Situ Hybridization, FluorescenceLaser Capture MicrodissectionMaleMolecular Sequence DataCathepsin DGranulocyte Colony-Stimulating FactorMutant ProteinsOLFM4 protein, human

Identifiers

PMID24070418
PMCPMC3791688
OpenAlexW2132493323

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.