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2.
Biol. Res ; 45(3): 223-230, 2012. ilus, tab
Article in English | LILACS | ID: lil-659280

ABSTRACT

The Sonic Hegdehog/GLI (SHH/GLI) pathway has been extensively studied for its role in developmental and cancer biology. During early embryonic development the SHH pathway is involved mainly in pattern formation, while in latter stages its function in stem cell and progenitor proliferation becomes increasingly relevant. During postnatal development and in adult tissues, SHH/GLI promotes cell homeostasis by actively regulating gene transcription, recapitulating the function observed during normal tissue growth. In this review, we will briefly discuss the fundamental importance of SHH/GLI in tumor growth and cancer evolution and we will then provide insights into a possible novel mechanism of SHH action in cancer through autophagy modulation in cancer stem cells. Autophagy is a homeostatic mechanism that when disrupted can promote and accelerate tumor progression in both cancer cells and the stroma that harbors tumorigenesis. Understanding possible new targets for SHH signaling and its contribution to cancer through modulation of autophagy might provide better strategies in order to design combined treatments and perform clinical trials.


Subject(s)
Humans , Autophagy/physiology , Hedgehog Proteins/physiology , Neoplastic Stem Cells/pathology , Neuroblastoma/physiopathology , Transcription Factors/physiology , Cell Line, Tumor , Cell Proliferation , Neuroblastoma/pathology , Neuroblastoma/therapy , Signal Transduction
3.
Biol. Res ; 44(1): 63-67, 2011. ilus
Article in English | LILACS | ID: lil-591865

ABSTRACT

Proliferation and cell fate determination in the developing embryo are extrinsically regulated by multiple interactions among diverse secreted factors, such as Sonic Hedgehog (SHh), which act in a concentration-dependent manner. The fact that SHh is secreted as a lipid-modified protein suggests the existence of a mechanism to regulate its movement across embryonic fields. We have previously shown that heparan sulfate proteoglycans (HSPGs) are required for SHh binding and signalling. However, it was not determined which specific HSPG was responsible for these functions. Here we evaluated the contribution of perlecan on SHh localization and activity. To understand the mechanism of action of perlecan at the cellular level, we studied the role of perlecan-SHh interaction in SHh activity using both cell culture and biochemical assays. Our findings show that perlecan is a crucial anchor and modulator of SHh activity acting as an extracellular positive regulator of SHh.


Subject(s)
Animals , Humans , Mice , Rats , Brain/drug effects , Heparan Sulfate Proteoglycans/pharmacology , Signal Transduction/drug effects , Brain/metabolism , Chromatography, Gel , Fibroblasts/drug effects , Fibroblasts/metabolism , Gene Expression Regulation, Developmental , Hedgehog Proteins/metabolism , Heparan Sulfate Proteoglycans/isolation & purification , Heparan Sulfate Proteoglycans/metabolism , Heparan Sulfate Proteoglycans/physiology , Immunohistochemistry
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