scholarly journals Hedgehog Inhibition Promotes a Switch from Type II to Type I Cell Death Receptor Signaling in Cancer Cells

PLoS ONE ◽  
2011 ◽  
Vol 6 (3) ◽  
pp. e18330 ◽  
Author(s):  
Satoshi Kurita ◽  
Justin L. Mott ◽  
Sophie C. Cazanave ◽  
Christian D. Fingas ◽  
Maria E. Guicciardi ◽  
...  
2005 ◽  
Vol 83 (5) ◽  
pp. 579-588 ◽  
Author(s):  
Claudio A Hetz ◽  
Vicente Torres ◽  
Andrew F.G Quest

Apoptosis is a morphologically defined form of programmed cell death (PCD) that is mediated by the activation of members of the caspase family. Analysis of death-receptor signaling in lymphocytes has revealed that caspase-dependent signaling pathways are also linked to cell death by nonapoptotic mechanisms, indicating that apoptosis is not the only form of PCD. Under physiological and pathological conditions, cells demonstrate a high degree of flexibility in cell-death responses, as is reflected in the existence of a variety of mechanisms, including necrosis-like PCD, autophagy (or type II PCD), and accidental necrosis. In this review, we discuss recent data suggesting that canonical apoptotic pathways, including death-receptor signaling, control caspase-dependent and -independent cell-death pathways.Key words: apoptosis, necrosis, nonapoptotic programmed cell death, death receptors, ceramides.


2005 ◽  
Vol 18 (6) ◽  
pp. 637-650 ◽  
Author(s):  
Shairaz Baksh ◽  
Stella Tommasi ◽  
Sarah Fenton ◽  
Victor C. Yu ◽  
L. Miguel Martins ◽  
...  

Cells ◽  
2021 ◽  
Vol 10 (11) ◽  
pp. 3100
Author(s):  
Jürgen Fritsch ◽  
Julia Frankenheim ◽  
Lothar Marischen ◽  
Timea Vadasz ◽  
Anja Troeger ◽  
...  

Signaling via death receptor family members such as TNF-R1 mediates pleiotropic biological outcomes ranging from inflammation and proliferation to cell death. Pro-survival signaling is mediated via TNF-R1 complex I at the cellular plasma membrane. Cell death induction requires complex IIa/b or necrosome formation, which occurs in the cytoplasm. In many cell types, full apoptotic or necroptotic cell death induction requires the internalization of TNF-R1 and receptosome formation to properly relay the signal inside the cell. We interrogated the role of the enzyme A disintegrin and metalloprotease 17 (ADAM17)/TACE (TNF-α converting enzyme) in death receptor signaling in human hematopoietic cells, using pharmacological inhibition and genetic ablation. We show that in U937 and Jurkat cells the absence of ADAM17 does not abrogate, but rather increases TNF mediated cell death. Likewise, cell death triggered via DR3 is enhanced in U937 cells lacking ADAM17. We identified ADAM17 as the key molecule that fine-tunes death receptor signaling. A better understanding of cell fate decisions made via the receptors of the TNF-R1 superfamily may enable us, in the future, to more efficiently treat infectious and inflammatory diseases or cancer.


2015 ◽  
Vol 6 (10) ◽  
pp. e1926-e1926 ◽  
Author(s):  
S Seah ◽  
I C C Low ◽  
J L Hirpara ◽  
K Sachaphibulkij ◽  
G Kroemer ◽  
...  

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