Evidence map›Paper›PMID 14578209›Full record

ArticleThe American journal of pathology2003

Progression to malignancy in the polyoma middle T oncoprotein mouse breast cancer model provides a reliable model for human diseases.

Elaine Y Lin, Joan G Jones, Ping Li, Liyin Zhu, Kathleen D Whitney, William J Muller, Jeffrey W Pollard

Abstract read
In one paragraph

Article in The American journal of pathology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 711 papers.

0numbers the graph read from it
0cells of the map it votes in
711citing 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

711 citing papers in PubMed.

  1. A Co-clinical Trial of Exercise Therapy in Breast Cancer Prevention.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
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651 more citing papers are in PubMed but not listed here.

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.

Elaine Y LinCenter for Study of Reproductive Biology and Women's Health, Departments of Developmental and Molecular Biology/Obstetrics and Gynecology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
Joan G Jones
Ping Li
Liyin Zhu
Kathleen D Whitney
William J Muller
Jeffrey W Pollard

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
CSF-1 Macrophages &Mammary Gland Development and CancerR01CA094173 · NCI · YESHIVA UNIVERSITY · PI POLLARD, JEFFREY W. · 2002 to 2006
$1.0M
AGING TRAINING GRANTT32AG000194 · NIA · YESHIVA UNIVERSITY · PI HAMERMAN, DAVID · 1989 to 1998
–
NCI NIH HHS P30 CA013330NCI NIH HHS P30 CA 13330NCI NIH HHS R01 CA 094173NCI NIH HHS R01 CA094173NIA NIH HHS 5T32 AG 00194NIA NIH HHS T32 AG000194
6 · The paper itself

Abstract

Animal models are powerful tools to analyze the mechanism of the induction of human breast cancer. Here we report a detailed analysis of mammary tumor progression in one mouse model of breast cancer caused by expression of the polyoma middle T oncoprotein (PyMT) in the mammary epithelium, and its comparison to human breast tumors. In PyMT mice, four distinctly identifiable stages of tumor progression from premalignant to malignant stages occur in a single primary tumor focus and this malignant transition is followed by a high frequency of distant metastasis. These stages are comparable to human breast diseases classified as benign or in situ proliferative lesions to invasive carcinomas. In addition to the morphological similarities with human breast cancer, the expression of biomarkers in PyMT-induced tumors is also consistent with those associated with poor outcome in humans. These include a loss of estrogen and progesterone receptors as well as integrin-beta1 expression and the persistent expression of ErbB2/Neu and cyclinD1 in PyMT-induced tumors as they progress to the malignant stage. An increased leukocytic infiltration was also closely associated with the malignant transition. This study demonstrates that the PyMT mouse model is an excellent one to understand the biology of tumor progression in humans.

Indexed as

Disease Models, AnimalTumor Virus InfectionsAnimalsAntigens, Viral, TumorBlotting, WesternCell Transformation, NeoplasticDisease ProgressionFemaleHumansImmunohistochemistryMammary Neoplasms, ExperimentalMiceMice, TransgenicOncogene ProteinsPolyomavirusPrecancerous ConditionsAntigens, Viral, TumorOncogene ProteinsReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID14578209
PMCPMC1892434

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.