Published 2002 | Version v1
Journal article

Progesterone receptors – animal models and cell signaling in breast cancer: The role of oestrogen and progesterone receptors in human mammary development and tumorigenesis

  • 1. Tumour Biochemistry Laboratory, Christie Hospital NHS Trust, Manchester (United Kingdom)

Description

A relatively small number of cells in the normal human mammary gland express receptors for oestrogen and progesterone (ER and PR), and there is almost complete dissociation between steroid receptor expression and proliferation. Increased expression of the ER alpha (ERα) and loss of the inverse relationship between receptor expression and proliferation occur at the very earliest stages of tumorigenesis, implying that dysregulation of ERα expression contributes to breast tumour formation. There is evidence also for alterations in the ratio between the two PR isoforms in premalignant breast lesions. Elucidation of the factors mediating the effects of oestradiol and progesterone on development of the normal breast and of the mechanisms by which expression of the ERα and the PR isoforms is controlled could identify new targets for breast cancer prevention and improved prediction of breast cancer risk

Availability note (English)

Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC138744

Additional details

Publishing Information

Journal Title
Breast Cancer Research (Print)
Journal Volume
4
Journal Issue
5
Journal Page Range
p. 197-201
ISSN
1465-5411

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
47007056
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
ANIMALS; EPITHELIUM; FORECASTING; HAZARDS; MAMMARY GLANDS; NEOPLASMS; PROGESTERONE; RECEPTORS
Descriptors DEC
ANIMAL TISSUES; BODY; DISEASES; GLANDS; HORMONES; KETONES; MEMBRANE PROTEINS; ORGANIC COMPOUNDS; ORGANS; PREGNANES; PROTEINS; STEROID HORMONES; STEROIDS

Optional Information

Copyright
Copyright (c) 2002 2002 BioMed Central Ltd
Notes
PMCID: PMC138744; PUBLISHER-ID: bcr452; PMID: 12223124; OAI: oai:pubmedcentral.nih.gov:138744