EP-1803: Comparative analysis of radiation-induced changes in gene expression and migration potential of HNSCC and PC cells

2014 ◽  
Vol 111 ◽  
pp. S290-S291
Author(s):  
K. Mäbert ◽  
I. Kurth ◽  
L. Hein ◽  
C. Peitzsch ◽  
M. Cojoc ◽  
...  
Nature ◽  
2009 ◽  
Vol 459 (7246) ◽  
pp. 587-591 ◽  
Author(s):  
Denis A. Smirnov ◽  
Michael Morley ◽  
Eunice Shin ◽  
Richard S. Spielman ◽  
Vivian G. Cheung

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Chi-Ming Lee ◽  
Yen-Hao Su ◽  
Thanh-Tuan Huynh ◽  
Wei-Hwa Lee ◽  
Jeng-Fong Chiou ◽  
...  

For many malignancies, radiation therapy remains the second option only to surgery in terms of its curative potential. However, radiation-induced tumor cell death is limited by a number of factors, including the adverse response of the tumor microenvironment to the treatment and either intrinsic or acquired mechanisms of evasive resistance, and the existence of cancer stem cells (CSCs). In this study, we demonstrated that using different doses of irradiation led to the enrichment of CD133+Mahlavu cells using flow cytometric method. Subsequently, CD133+Mahlavu cells enriched by irradiation were characterized for their stemness gene expression, self-renewal, migration/invasion abilities, and radiation resistance. Having established irradiation-enriched CD133+Mahlavu cells with CSC properties, we evaluated a phytochemical, pterostilbene (PT), found abundantly in blueberries, against irradiation-enriched CSCs. It was shown that PT treatment dose-dependently reduced the enrichment of CD133+Mahlavu cells upon irradiation; PT treatment also prevented tumor sphere formation, reduced stemness gene expression, and suppressed invasion and migration abilities as well as increasing apoptosis of CD133+Mahlavu CSCs. Based on our experimental data, pterostilbene could be used to prevent the enrichment of CD133+hepatoma CSCs and should be considered for future clinical testing as a combined agent for HCC patients.


2005 ◽  
Vol 14 (6) ◽  
pp. 665-674 ◽  
Author(s):  
J. Huang ◽  
X. Miao ◽  
W. Jin ◽  
P. Couble ◽  
Y. Zhang ◽  
...  

2005 ◽  
Vol 65 (22) ◽  
pp. 10389-10393 ◽  
Author(s):  
Kevin Camphausen ◽  
Benjamin Purow ◽  
Mary Sproull ◽  
Tamalee Scott ◽  
Tomoko Ozawa ◽  
...  

Blood ◽  
2009 ◽  
Vol 114 (14) ◽  
pp. 2900-2908 ◽  
Author(s):  
Maheswaran Mani ◽  
Shivkumar Venkatasubrahmanyam ◽  
Mrinmoy Sanyal ◽  
Shoshana Levy ◽  
Atul Butte ◽  
...  

The pleiotropic receptor tyrosine kinase Kit can provide cytoskeletal signals that define cell shape, positioning, and migration, but the underlying mechanisms are less well understood. In this study, we provide evidence that Kit signals through Wiskott-Aldrich syndrome protein (WASP), the central hematopoietic actin nucleation-promoting factor and regulator of the cytoskeleton. Kit ligand (KL) stimulation resulted in transient tyrosine phosphorylation of WASP, as well as interacting proteins WASP-interacting protein and Arp2/3. KL-induced filopodia in bone marrow–derived mast cells (BMMCs) were significantly decreased in number and size in the absence of WASP. KL-dependent regulation of intracellular Ca2+ levels was aberrant in WASP-deficient BMMCs. When BMMCs were derived from WASP-heterozygous female mice using KL as a growth factor, the cultures eventually developed from a mixture of WASP-positive and -negative populations into a homogenous WASP-positive culture derived from the WASP-positive progenitors. Thus, WASP expression conferred a selective advantage to the development of Kit-dependent hematopoiesis consistent with the selective advantage of WASP-positive hematopoietic cells observed in WAS-heterozygous female humans. Finally, KL-mediated gene expression in wild-type and WASP-deficient BMMCs was compared and revealed that approximately 30% of all Kit-induced changes were WASP dependent. The results indicate that Kit signaling through WASP is necessary for normal Kit-mediated filopodia formation, cell survival, and gene expression, and provide new insight into the mechanism in which WASP exerts a strong selective pressure in hematopoiesis.


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