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Title: Epigenetic reversion of breast carcinoma phenotype is accompaniedby DNA sequestration

Journal Article · · American Journal of Pathology
OSTI ID:929485

The importance of microenvironment and context in regulation of tissue-specific genes is finally well established. DNA exposure to, or sequestration from, nucleases can be used to detect differences in higher order chromatin structure in intact cells without disturbing cellular or tissue architecture. To investigate the relationship between chromatin organization and tumor phenotype, we utilized an established 3-D assay where normal and malignant human breast cells can be easily distinguished by the morphology of the structures they make (acinus-like vs tumor-like, respectively). We show that these phenotypes can be distinguished also by sensitivity to AluI digestion where the malignant cells are resistant to digestion relative to non-malignant cells. Reversion of the T4-2 breast cancer cells by either cAMP analogs, or a phospatidylinositol 3-kinase (P13K) inhibitor not only reverted the phenotype, but also the chromatin sensitivity to AluI. By using different cAMP-analogs, we show that the cAMP-induced phenotypic reversion, polarization, and shift in DNA organization act through a cAMP-dependent-protein-kinase A-coupled signaling pathway. Importantly, inhibitory antibody to fibronectin also reverted the malignant phenotype, polarized the acini, and changed chromatin sequestration. These experiments show not only that modifying the tumor microenvironment can alter the organization of tumor cells but also that architecture of the tissues and the global chromatin organization are coupled and yet highly plastic.

Research Organization:
Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE Director. Office of Science. Biological andEnvironmental Research
DOE Contract Number:
DE-AC02-05CH11231
OSTI ID:
929485
Report Number(s):
LBNL-62308; AJPAA4; R&D Project: 443180; BnR: KP1104010; TRN: US200813%%210
Journal Information:
American Journal of Pathology, Vol. 170, Issue 5; Related Information: Journal Publication Date: 05/2007; ISSN 0002-9440
Country of Publication:
United States
Language:
English