Evidence map›Paper›PMID 9177224›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1997

Tissue-specific expression of the human prostate-specific antigen gene in transgenic mice: implications for tolerance and immunotherapy.

C Wei, R A Willis, B R Tilton, R J Looney, E M Lord, R K Barth, J G Frelinger

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 79 citations in OpenAlex.

  1. A simple urine test by 3D-plus-3D immunoassay guides preciseBioengineering & translational medicine · 2023
    Article
  2. Review
  3. Article
  4. Drug discovery in prostate cancer mouse models.Expert opinion on drug discovery · 2015
    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

7 authors at 1 institution in 1 country.

C WeiDepartment of Microbiology and Immunology and the Cancer Center, University of Rochester Medical Center, Rochester, NY 14642, USA.
R A Willis
B R Tilton
R J Looney
E M Lord
R K Barth
J G Frelinger
University of Rochester Medical Center · US

Funding

The T32 Predoctoral Training Program in Immunology (PTPI)T32AI007285 · NIAID · UNIVERSITY OF ROCHESTER · PI Scott Andrew Gerber, JACQUES Robert · 1986 to 2026
$7.6M
IN SITU ANTITUMOR IMMUNITY AND EFFECTS OF RADIATIONR01CA028332 · NCI · UNIVERSITY OF ROCHESTER · PI LORD, EDITH M · 1985 to 2020
$5.0M
CANCER RESEARCH TRAINING-EXPERIMENTAL THERAPY MODELST32CA009363 · NCI · UNIVERSITY OF ROCHESTER · PI LAND, HARTMUT · 1985 to 2013
$2.9M
TARGETED CTL MEDIATED IMMUNITY FOR PROSTATE CANCERR01CA070218 · NCI · UNIVERSITY OF ROCHESTER · PI FRELINGER, JOHN G. · 1996 to 2001
$498k
NCI NIH HHS CA28332NCI NIH HHS CA70218NCI NIH HHS R01 CA028332NCI NIH HHS T32 CA009363NCI NIH HHS T32CA09363NIAID NIH HHS T32 AI007285
6 · The paper itself

Abstract

Human prostate-specific antigen (PSA) has been widely used as a serum marker for cancer of the prostate. The cell type-specific expression of PSA also makes it a potential tumor antigen for prostate cancer immunotherapy. Study of the immunological aspects of PSA within either normal or malignant prostate tissue has been hampered by the lack of a mouse model, because no PSA counterpart has been identified in mice. Using a 14-kb genomic DNA region that encompasses the entire human PSA gene and adjacent flanking sequences, we generated a series of human PSA transgenic mice. In the six independent lines of transgenic mice generated, the expression of the human PSA transgene, driven by its own cis-acting regulatory elements, is specifically targeted to the prostate. Tissue distribution analysis demonstrated that PSA transgene expression closely follows the human expression pattern. Immunohistochemical analysis of the prostate tissue also showed that the expression of the PSA transgene is confined to the ductal epithelial cells. Despite expressing PSA as a self-antigen in the prostate, these transgenic mice were able to mount a cytotoxic immune response against PSA expressed by tumor cells, indicating that expression of the transgene has not resulted in complete nonresponsiveness. This transgenic mouse model will provide a well defined system to gain an insight into the mechanisms of nonresponsiveness to PSA, ultimately leading to strategies for immunotherapy of human prostate cancer using PSA as the target antigen.

Indexed as

Transcription, GeneticAnimalsCell LineCytotoxicity, ImmunologicDNA PrimersGenetic TherapyGenitalia, MaleHumansImmunosuppression TherapyImmunotherapyMaleMiceMice, TransgenicOrgan SpecificityPolymerase Chain ReactionProstate-Specific AntigenDNA PrimersProstate-Specific AntigenRecombinant ProteinsRNA, Messenger

Identifiers

PMID9177224
PMCPMC21056
OpenAlexW2005953810

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.