Activated type I TGFβ receptor kinase enhances the survival of mammary epithelial cells and accelerates tumor progression

RS Muraoka-Cook, I Shin, JY Yi, E Easterly… - Oncogene, 2006 - nature.com
RS Muraoka-Cook, I Shin, JY Yi, E Easterly, MH Barcellos-Hoff, JM Yingling, R Zent
Oncogene, 2006nature.com
We have examined the effects of transforming growth factor-beta (TGFβ) signaling on
mammary epithelial cell survival. Transgenic mice expressing an active mutant of Alk5 in the
mammary gland (MMTV-Alk5 T204D) exhibited reduced apoptosis in terminal endbuds and
during postlactational involution. Transgene-expressing mammary cells contained lower
Smad2/3 and higher c-myc levels than controls, high ligand-independent
phosphatidylinositol-3 kinase (PI3K) and Akt activities, and were insensitive to TGFβ …
Abstract
We have examined the effects of transforming growth factor-beta (TGFβ) signaling on mammary epithelial cell survival. Transgenic mice expressing an active mutant of Alk5 in the mammary gland (MMTV-Alk5 T204D) exhibited reduced apoptosis in terminal endbuds and during postlactational involution. Transgene-expressing mammary cells contained lower Smad2/3 and higher c-myc levels than controls, high ligand-independent phosphatidylinositol-3 kinase (PI3K) and Akt activities, and were insensitive to TGFβ-mediated growth arrest. Treatment with a proteasome inhibitor increased Smad2/3 levels and ligand-independent Smad transcriptional reporter activity, as well as reduced both c-myc protein and basal cell proliferation. Treatment with an Alk5 kinase small-molecule inhibitor upregulated Smad2/3 levels, reduced PI3K activity, P-Akt, and c-myc, and inhibited cell survival. Although Alk5 T204D-expressing mice did not develop mammary tumors, bigenic MMTV-Alk T204D× Neu mice developed cancers that were more metastatic than those occurring in MMTV-Neu transgenics. These data suggest that (1) TGFβ can signal to PI3K/Akt and enhance mammary epithelial cell survival in vivo before cytological or histological evidence of transformation, and (2) TGFβ signaling can provide epithelial cells with a ‘gain-of-function’effect that synergizes with oncogene-induced transformation.
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