Published September 3, 2004 | Version v1
Journal article

A transcriptional repressor of osteopontin expression in the 4T1 murine breast cancer cell line

  • 1. Department of Surgery, Duke University Medical Center, Durham, NC 27710 (United States)

Description

Osteopontin (OPN) is a highly hydrophilic and negatively charged sialoprotein of ∼298 amino acids which is an important mediator of tumor metastatic behavior. We have previously demonstrated that endotoxin-dependent OPN gene transcription is regulated by a constitutive transcriptional repressor protein, heterogeneous nuclear ribonucleoprotein A/B (hnRNP-A/B). However, in the context of cancer, the role of hnRNP-A/B in the transcriptional regulation of OPN and its metastasis-promoting functions has not been previously studied. We examined hnRNP-A/B in the 4T1 murine mammary epithelial tumor cell line, a thioguanine resistant subline which closely mimics stage IV breast cancer in humans. Our data indicate that hnRNP-A/B p37 binds to the OPN promoter, significantly decreases OPN promoter activity and mRNA levels, ablates OPN protein expression, and inhibits OPN dependent in vitro correlates of metastatic behavior, motility, and invasion. These results are unique and may suggest new therapies to re-establish loco-regional control of cancers

Additional details

Identifiers

DOI
10.1016/j.bbrc.2004.07.063;
PII
S0006-291X(04)01561-X;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
321
Journal Issue
4
Journal Page Range
p. 1010-1016
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
36052608
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
AMINO ACIDS; GENE REGULATION; IN VITRO; MAMMARY GLANDS; METASTASES; NEOPLASMS; PROTEINS; THERAPY; TRANSCRIPTION; TUMOR CELLS
Descriptors DEC
ANIMAL CELLS; BODY; CARBOXYLIC ACIDS; DISEASES; GLANDS; MEDICINE; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANS

Optional Information

Copyright
Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.