The function of SEC22B and its role in human diseases
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 m...
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| Veröffentlicht in: | Cytoskeleton (Hoboken, N.J.) N.J.), 2020-08, Vol.77 (8), p.303-312 |
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| creator | Sun, Wei Tian, Bi‐Xia Wang, Shu‐Hong Liu, Pei‐Jun Wang, Yao‐Chun |
| description | 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. |
| doi_str_mv | 10.1002/cm.21628 |
| format | Article |
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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. 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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.</description><subject>Antigen presentation</subject><subject>Autophagy</subject><subject>cancer</subject><subject>Cell fusion</subject><subject>Cytokinesis</subject><subject>Endoplasmic reticulum</subject><subject>Golgi</subject><subject>Golgi apparatus</subject><subject>Membrane fusion</subject><subject>Membrane trafficking</subject><subject>Phagocytosis</subject><subject>Proteins</subject><subject>SEC22B</subject><subject>SNAP receptors</subject><subject>SNARE</subject><subject>Synaptic transmission</subject><subject>vesicle trafficking</subject><issn>1949-3584</issn><issn>1949-3592</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLw0AUhQdRbK2Cv0AG3LhJvfNKZpYa6gMqLqzrYTK5oSl51EyD9N8bbVUQXN27-Pg45xByzmDKAPi1r6ecxVwfkDEz0kRCGX7482s5IichrABiI0Ack5HgidQqYWOiFkukRd_4Tdk2tC3oyyzl_Ja6JqflJtCurZCWDV32tWtoXgZ0AcMpOSpcFfBsfyfk9W62SB-i-fP9Y3ozjzw3WkfIJOQqE8x4nwsAlmnpTCY4zzMHICVyDnGR-zhWCg3ECcZCqoI7yVmSCDEhVzvvumvfegwbW5fBY1W5Bts-WC6HPonWkg3o5R901fZdM6QbKKlhKJyoX6Hv2hA6LOy6K2vXbS0D-zml9bX9mnJAL_bCPqsx_wG_txuAaAe8lxVu_xXZ9Gkn_ABa23eY</recordid><startdate>202008</startdate><enddate>202008</enddate><creator>Sun, Wei</creator><creator>Tian, Bi‐Xia</creator><creator>Wang, Shu‐Hong</creator><creator>Liu, Pei‐Jun</creator><creator>Wang, Yao‐Chun</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3430-0058</orcidid></search><sort><creationdate>202008</creationdate><title>The function of SEC22B and its role in human diseases</title><author>Sun, Wei ; Tian, Bi‐Xia ; Wang, Shu‐Hong ; Liu, Pei‐Jun ; Wang, Yao‐Chun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2988-e140d5b319ccd3001b84a9b322dba0044e2206fdc6655e9067e6345f2a4217733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antigen presentation</topic><topic>Autophagy</topic><topic>cancer</topic><topic>Cell fusion</topic><topic>Cytokinesis</topic><topic>Endoplasmic reticulum</topic><topic>Golgi</topic><topic>Golgi apparatus</topic><topic>Membrane fusion</topic><topic>Membrane trafficking</topic><topic>Phagocytosis</topic><topic>Proteins</topic><topic>SEC22B</topic><topic>SNAP receptors</topic><topic>SNARE</topic><topic>Synaptic transmission</topic><topic>vesicle trafficking</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun, Wei</creatorcontrib><creatorcontrib>Tian, Bi‐Xia</creatorcontrib><creatorcontrib>Wang, Shu‐Hong</creatorcontrib><creatorcontrib>Liu, Pei‐Jun</creatorcontrib><creatorcontrib>Wang, Yao‐Chun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cytoskeleton (Hoboken, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Wei</au><au>Tian, Bi‐Xia</au><au>Wang, Shu‐Hong</au><au>Liu, Pei‐Jun</au><au>Wang, Yao‐Chun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The function of SEC22B and its role in human diseases</atitle><jtitle>Cytoskeleton (Hoboken, N.J.)</jtitle><addtitle>Cytoskeleton (Hoboken)</addtitle><date>2020-08</date><risdate>2020</risdate><volume>77</volume><issue>8</issue><spage>303</spage><epage>312</epage><pages>303-312</pages><issn>1949-3584</issn><eissn>1949-3592</eissn><abstract>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.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>32748571</pmid><doi>10.1002/cm.21628</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-3430-0058</orcidid><oa>free_for_read</oa></addata></record> |
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| subjects | Antigen presentation Autophagy cancer Cell fusion Cytokinesis Endoplasmic reticulum Golgi Golgi apparatus Membrane fusion Membrane trafficking Phagocytosis Proteins SEC22B SNAP receptors SNARE Synaptic transmission vesicle trafficking |
| title | The function of SEC22B and its role in human diseases |
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