The function of SEC22B and its role in human diseases
The function of SEC22B and its role in human diseases
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SEC22B的功能及其在人类疾病中的作用
DOI:
10.1002/cm.21628
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发表时间:
2020-08
期刊:
影响因子:
2.9
通讯作者:
Yao‐Chun Wang
中科院分区:
文献类型:
--
作者:
Wei Sun;Bi‐Xia Tian;Shu‐Hong Wang;Pei‐Jun Liu;Yao‐Chun Wang
Soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) proteins.are a large protein complex that is involved in the membrane fusion in vesicle.trafficking, cell growth, cytokinesis, membrane repair, and synaptic transmission. As.one of the SNARE proteins, SEC22B functions in membrane fusion of vesicle trafficking.between the endoplasmic reticulum and the Golgi apparatus, antigen cross-presentation,.secretory autophagy, and other biological processes. However, apart from.not being SNARE proteins, there is little knowledge known about its two homologs.(SEC22A and SEC22C). SEC22B alterations have been reported in many human diseases,.especially, many mutations of SEC22B in human cancers have been detected..In this review, we will introduce the specific functions of SEC22B, and summarize the.researches about SEC22B in human cancers and other diseases. These findings have.laid the foundation for further studies to clarify the exact mechanism of SEC22B in.the pathological process and to seek new therapeutic targets and better treatment.strategies.
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影响因子:
7.3
作者:
Gao J;Aksoy BA;Dogrusoz U;Dresdner G;Gross B;Sumer SO;Sun Y;Jacobsen A;Sinha R;Larsson E;Cerami E;Sander C;Schultz N
通讯作者:
Schultz N
DOI:
10.1177/1533317515588181
发表时间:
2016-03
期刊:
American Journal of Alzheimer's Disease & Other Dementias
影响因子:
--
作者:
Yanxin Zhao;W. Tan;Wenhua Sheng;Xiaohong Li
通讯作者:
Yanxin Zhao;W. Tan;Wenhua Sheng;Xiaohong Li
影响因子:
7.3
作者:
Collins LE;DeCourcey J;Soledad di Luca M;Rochfort KD;Loscher CE
通讯作者:
Loscher CE
DOI:
10.1084/jem.20170229
发表时间:
2017-08-07
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Alloatti A;Rookhuizen DC;Joannas L;Carpier JM;Iborra S;Magalhaes JG;Yatim N;Kozik P;Sancho D;Albert ML;Amigorena S
通讯作者:
Amigorena S
影响因子:
64.8
作者:
Zhou Q;Zhou P;Wang AL;Wu D;Zhao M;Südhof TC;Brunger AT
通讯作者:
Brunger AT