Title of article :
Transketolase-like protein 1 confers resistance to serum withdrawal in vitro
Author/Authors :
Hartmannsberger، نويسنده , , Diana and Mack، نويسنده , , Brigitte and Eggert، نويسنده , , Carola and Denzel، نويسنده , , Sabine and Stepp، نويسنده , , Herbert and Betz، نويسنده , , Christian S. and Gires، نويسنده , , Olivier، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
10
From page :
20
To page :
29
Abstract :
Transketolase-like protein 1 (TKTL1) is a member of the family of transketolase enzymes of which the founder member transketolase (TKT) is known to play a central role in the non-oxidative part of the pentose phosphate pathway. According to several publications TKTL1 is the only family member, whose expression is substantially de-regulated in a variety of solid tumours. Over-expression of TKTL1 correlates with poor prognosis of cancer patients and TKTL1 itself represents a potential therapeutic target owing to its possible involvement in the regulation of the proliferation and metabolism of cancer cells. We show that exogenously expressed TKTL1 provides HEK293 cells with moderate growth advantages under standard culture conditions, while protecting cells from growth factor withdrawal-induced apoptosis. Importantly, we identified TKTL1 with the JFC12T10 antibody as a 65 kDa protein, which was however absent in most tumour cell lines tested. Primary head and neck squamous cell carcinomas of various localisations were characterised by a focal pattern with single cells strongly expressing TKTL1, rather than by a homogeneous expression pattern within the tumour mass.
Keywords :
carcinoma , pentose phosphate pathway , TKTL1
Journal title :
Cancer Letters
Serial Year :
2011
Journal title :
Cancer Letters
Record number :
1819397
Link To Document :
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