Evidence map›Paper›PMID 30082453›Full record

ReviewCold Spring Harbor perspectives in medicine2019

Molecular Pathology of High-Grade Prostatic Intraepithelial Neoplasia: Challenges and Opportunities.

Levent Trabzonlu, Ibrahim Kulac, Qizhi Zheng, Jessica L Hicks, Michael C Haffner, William G Nelson, Karen S Sfanos, Onur Ertunc, Tamara L Lotan, Christopher M Heaphy and 3 more

Open access · bronzeAbstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed, 37 citations in OpenAlex.

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  14. Preliminary study on miRNA in prostate cancer.World journal of surgical oncology · 2023
    Article
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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

13 authors at 4 institutions in 2 countries.

Levent TrabzonluDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Ibrahim KulacDepartment of Pathology, Koc University School of Medicine, Istanbul 34010, Turkey.
Qizhi ZhengDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Jessica L HicksDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Michael C HaffnerDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
William G NelsonDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Karen S SfanosDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Onur ErtuncDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Tamara L LotanDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Christopher M HeaphyDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Alan K MeekerDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Srinivasan YegnasubramanianSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287.
Angelo M De MarzoDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Johns Hopkins University · USSidney Kimmel Comprehensive Cancer Center · USJohns Hopkins Medicine · USKoç University · TR

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI WILLIAM George NELSON · 1985 to 2026
$208.6M
TRANSGENIC MODELS FOR PROSTATE CANCER AND AUTOIMMUNITYP50CA058236 · NCI · JOHNS HOPKINS UNIVERSITY · PI DENMEADE, SAMUEL R · 1992 to 2020
$43.9M
Multidiciplinary Integrative Genomic Approach to Distinguish Lethal from Indolent Prostate Cancer in Men of Europena and African AncestryU01CA196390 · NCI · JOHNS HOPKINS UNIVERSITY · PI DE MARZO, ANGELO MICHAEL, PIENTA, KENNETH J. · 2015 to 2020
$5.8M
NCI NIH HHS P30 CA006973NCI NIH HHS P50 CA058236NCI NIH HHS U01 CA196390
6 · The paper itself

Abstract

A better understanding of the early stages of prostate cancer initiation, potentially arising from precursor lesions, may fuel development of powerful approaches for prostate cancer prevention or interception. The best-known candidate for such a precursor lesion has been referred to as high-grade prostatic intraepithelial neoplasia (HGPIN). Although there is significant evidence supporting the notion that such HGPIN lesions can give rise to invasive adenocarcinomas of the prostate, there are also numerous complicating considerations and evidence that cloud the picture in many instances. Notably, recent evidence has suggested that some fraction of such lesions that are morphologically consistent with HGPIN may actually be invasive carcinomas masquerading as HGPIN-a state that we term "postinvasive intraepithelial carcinoma" (PIC). Although the prevalence of such PIC lesions is not fully understood, this and other factors can confound the potential of identifying prostate precursors that can be targeted for disease prevention, interception, or treatment. Here, we review our current understanding of the morphological and molecular pathological features of prostate cancer precursor lesions.

Indexed as

AdenocarcinomaAnimalsCarcinoma, Intraductal, NoninfiltratingDiagnosis, DifferentialHumansMalePathology, MolecularProstatic Intraepithelial NeoplasiaProstatic Neoplasms

Identifiers

PMID30082453
PMCPMC6444695
OpenAlexW2886976164

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.