Regulation of cell death by sphingosine 1-phosphate lyase
被引:6
作者:
Colie, Sandra
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机构:
Fac Med Toulouse, INSERM, U858, F-31073 Toulouse, France
Univ Toulouse 3, Inst Med Mol Rangueil, IFR150, F-31062 Toulouse, FranceFac Med Toulouse, INSERM, U858, F-31073 Toulouse, France
Colie, Sandra
[1
,2
]
Codogno, Patrice
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机构:
INSERM, U756, Chatenay Malabry, FranceFac Med Toulouse, INSERM, U858, F-31073 Toulouse, France
Codogno, Patrice
[3
]
Levade, Thierry
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机构:
Fac Med Toulouse, INSERM, U858, F-31073 Toulouse, France
Univ Toulouse 3, Inst Med Mol Rangueil, IFR150, F-31062 Toulouse, FranceFac Med Toulouse, INSERM, U858, F-31073 Toulouse, France
Levade, Thierry
[1
,2
]
Andrieu-Abadie, Nathalie
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h-index: 0
机构:
Fac Med Toulouse, INSERM, U858, F-31073 Toulouse, France
Univ Toulouse 3, Inst Med Mol Rangueil, IFR150, F-31062 Toulouse, FranceFac Med Toulouse, INSERM, U858, F-31073 Toulouse, France
Andrieu-Abadie, Nathalie
[1
,2
]
机构:
[1] Fac Med Toulouse, INSERM, U858, F-31073 Toulouse, France
[2] Univ Toulouse 3, Inst Med Mol Rangueil, IFR150, F-31062 Toulouse, France
By controlling sphingosine 1-phosphate (S1P) catabolism, S1P lyase (SPL) represents an undeniable candidate as potential regulator of a cancer cell's fate in response to stress. Our recent study reveals that complete loss of SPL activity leads to upregulation of the antiapoptotic proteins Bcl-2 and Bcl-x(L) and consequently protects against apoptosis induced by chemotherapy and nutrient starvation but not against autophagy. Here, we speculate on how S1P and disruption of S1P breakdown may regulate cell death and autophagy.