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Aldo-keto reductase family 1, member B10 is secreted through a lysosome-mediated non-classical pathway

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成果类型:
期刊论文
作者:
Luo, Di-xian;Huang, Mei C.;Ma, Jun;Gao, Zachary;Liao, Duan-fang*;...
通讯作者:
Liao, Duan-fang
作者机构:
[Liao, Duan-fang; Luo, Di-xian] Univ S China, Coll Pharm & Life Sci, Inst Pharm & Pharmacol, Hengyang 421001, Peoples R China.
[Luo, Di-xian; Ma, Jun; Gao, Zachary; Cao, Deliang] So Illinois Univ, Sch Med, Simmons Canc Inst, Dept Med Microbiol Immunol & Cell Biol, Springfield, IL 62794 USA.
[Huang, Mei C.] Mem Med Ctr, Dept Internal Med, Div Gastroenterol, Springfield, IL 62781 USA.
[Liao, Duan-fang] Hunan Univ Chinese Med, Sch Pharm, Dept Tradit Chinese Diagnost, Changsha 420108, Hunan, Peoples R China.
通讯机构:
[Liao, Duan-fang] U
Univ S China, Coll Pharm & Life Sci, Inst Pharm & Pharmacol, Hengyang 421001, Peoples R China.
语种:
英文
关键词:
aldo-keto reductase family 1;member B10 (AKR1B10);ATP-binding-cassette transporter (ABC transporter);calcium signalling;cancer marker;lysosomal exocytosis;non-classical protein-secretion pathway
期刊:
Biochemical Journal
ISSN:
0264-6021
年:
2011
卷:
438
期:
1
页码:
71-80
基金类别:
National Cancer InstituteUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Cancer Institute (NCI) [CA122622]; Department of DefenseUnited States Department of Defense [BC083555]; NATIONAL CANCER INSTITUTEUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Cancer Institute (NCI) [R21CA122622, R21CA122622] Funding Source: NIH RePORTER
机构署名:
本校为其他机构
院系归属:
中医学院
药学院
摘要:
AKR1B10 (aldo-keto reductase family 1, member B10) protein is primarily expressed in normal human small intestine and colon, but overexpressed in several types of human cancers and considered as a tumour marker. In the present study, we found that AKR1B10 protein is secreted from normal intestinal epithelium and cultured cancer cells, as detected by a newly developed sandwich ELISA and Western blotting. The secretion of AKR1B10 was not affected by the protein-synthesis inhibitor cycloheximide and the classical protein-secretion pathway inhibito...

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