Sulf2 gene is alternatively spliced in mammalian developing and tumour tissues with functional implications

被引:15
作者
Gill, Rai B. S. [1 ]
Day, Amy [1 ]
Barstow, Amy [1 ]
Liu, Hongxiang [2 ,3 ]
Zaman, Gul [1 ]
Dhoot, Gurtej K. [1 ]
机构
[1] Univ London Royal Vet Coll, Dept Basic Sci, London NW1 OTU, England
[2] Cambridge Univ NHS Fdn Trust, Addenbrookes Hosp, Mol Malignancy Lab, Cambridge, England
[3] Cambridge Univ NHS Fdn Trust, Addenbrookes Hosp, Dept Histopathol, Cambridge, England
基金
英国惠康基金;
关键词
Sulf2; Alternative splicing; Fetal development; Tumour growth; EGFR; cMet; pERK; pAKT; C-MET; GROWTH; CANCER; CARCINOMA; SULFATASE; PROTEINS; RECEPTOR; QSULF1; LUNG; HEAD;
D O I
10.1016/j.bbrc.2011.09.088
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SULF2 enzyme regulates the activities of a number of signalling pathways that in many tissues are up-regulated during development and disease. As we recently showed for avian Sulf1, the present study demonstrates that mammalian Sulf2 gene can also generate functionally distinct splice variants that would regulate normal development and tumour growth differentially. It is thus important to distinguish SULF1/SULF2 isoforms in mammalian tissues to understand their functional and clinical relevance to disease. This study demonstrates that unlike normal adult lung with little or no SULF2 expression, this enzyme is expressed at high levels in most lung tumours showing differential cellular distribution of full length and shorter SULF2 variants in such tumours. Furthermore, we show that the short SULF2 splice variants are associated with those signalling pathways that are inhibited by full length SULF1/SULF2 variants and therefore could promote growth in such lung tumours. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:468 / 473
页数:6
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