Breast cancer-associated fibroblasts confer AKT1-mediated epigenetic silencing of Cystatin M in epithelial cells
Journal
Cancer Research
Journal Volume
68
Journal Issue
24
Pages
10257-10266
Date Issued
2008
Author(s)
Lin H.-J.L.
Zuo T.
Chieh T.K.
Liyanarachchi S.
Sun S.
Shen R.
Deatherage D.E.
Potter D.
Asamoto L.
Lin S.
Yan P.S.
Ostrowski M.C.
Huang T.H.-M.
Abstract
The interplay between histone modifications and promoter hypermethylation provides a causative explanation for epigenetic gene silencing in cancer. Less is known about the upstream initiators that direct this process. Here, we report that the Cystatin M (CST6) tumor suppressor gene is concurrently down-regulated with other loci in breast epithelial cells cocultured with cancer-associated fibroblasts (CAF). Promoter hypermethylation of CST6 is associated with aberrant AKT1 activation in epithelial cells, as well as the disabled INNP4B regulator resulting from the suppression by CAFs. Repressive chromatin, marked by trimethyl-H3K27 and dimethyl-H3K9, and de novo DNA methylation is established at the promoter. The findings suggest that microenvironmental stimuli are triggers in this epigenetic cascade, leading to the long-term silencing of CST6 in breast tumors. Our present findings implicate a causal mechanism defining how tumor stromal fibroblasts support neoplastic progression by manipulating the epigenome of mammary epithelial cells. The result also highlights the importance of direct cell-cell contact between epithelial cells and the surrounding fibroblasts that confer this epigenetic perturbation. Because this two-way interaction is anticipated, the described coculture system can be used to determine the effect of epithelial factors on fibroblasts in future studies. ?2008 American Association for Cancer Research.
SDGs
Other Subjects
protein Akt 1; protein kinase B; unclassified drug; article; breast cancer; breast epithelium; cancer growth; cell interaction; chromatin; coculture; controlled study; cystatin m gene; DNA methylation; enzyme activation; enzyme phosphorylation; epigenetics; epithelium cell; female; fibroblast; gene silencing; human; human cell; human tissue; hypermethylation; microenvironment; priority journal; promoter region; tumor suppressor gene; Breast Neoplasms; Cell Communication; Cell Line, Tumor; Coculture Techniques; Cystatin M; DNA Methylation; Down-Regulation; Enzyme Activation; Epithelial Cells; Female; Fibroblasts; Gene Expression Regulation, Neoplastic; Gene Silencing; Humans; Promoter Regions, Genetic; Proto-Oncogene Proteins c-akt; Signal Transduction; Transfection
Type
journal article