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Rab1 in Cell Signaling, Cancer and Other Diseases

The ER and Golgi membrane system plays major roles in cell signaling and regulation of the biosynthesis/transport of proteins and lipids in response to environmental cues such as amino acid and cholesterol levels. Rab1 is the founding member of the Rab small GTPase family, which is known to mediate...

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Detalles Bibliográficos
Autores principales: Yang, Xianzhi, Li, Xiaoxing, Zhang, Yanjie, Rodriguez-Rodriguez, Lorna, Xiang, Mengqing, Wang, Hui-Yun, Zheng, X.F. Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396462/
https://www.ncbi.nlm.nih.gov/pubmed/27041585
http://dx.doi.org/10.1038/onc.2016.81
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author Yang, Xianzhi
Li, Xiaoxing
Zhang, Yanjie
Rodriguez-Rodriguez, Lorna
Xiang, Mengqing
Wang, Hui-Yun
Zheng, X.F. Steven
author_facet Yang, Xianzhi
Li, Xiaoxing
Zhang, Yanjie
Rodriguez-Rodriguez, Lorna
Xiang, Mengqing
Wang, Hui-Yun
Zheng, X.F. Steven
author_sort Yang, Xianzhi
collection PubMed
description The ER and Golgi membrane system plays major roles in cell signaling and regulation of the biosynthesis/transport of proteins and lipids in response to environmental cues such as amino acid and cholesterol levels. Rab1 is the founding member of the Rab small GTPase family, which is known to mediate dynamic membrane trafficking between ER and Golgi. Growing evidence indicate that Rab1 proteins have important functions beyond their classical vesicular transport functions, including nutrient sensing and signaling, cell migration, and presentation of cell surface receptors. Moreover, deregulation of RAB1 expression has been linked to a myriad of human diseases such as cancer, cardiomyopathy and Parkinson’s disease. Further investigating these new physiological and pathological functions of Rab1 should provide new opportunities for better understanding of the disease processes and may lead to more effective therapeutic interventions.
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spelling pubmed-53964622017-04-20 Rab1 in Cell Signaling, Cancer and Other Diseases Yang, Xianzhi Li, Xiaoxing Zhang, Yanjie Rodriguez-Rodriguez, Lorna Xiang, Mengqing Wang, Hui-Yun Zheng, X.F. Steven Oncogene Article The ER and Golgi membrane system plays major roles in cell signaling and regulation of the biosynthesis/transport of proteins and lipids in response to environmental cues such as amino acid and cholesterol levels. Rab1 is the founding member of the Rab small GTPase family, which is known to mediate dynamic membrane trafficking between ER and Golgi. Growing evidence indicate that Rab1 proteins have important functions beyond their classical vesicular transport functions, including nutrient sensing and signaling, cell migration, and presentation of cell surface receptors. Moreover, deregulation of RAB1 expression has been linked to a myriad of human diseases such as cancer, cardiomyopathy and Parkinson’s disease. Further investigating these new physiological and pathological functions of Rab1 should provide new opportunities for better understanding of the disease processes and may lead to more effective therapeutic interventions. 2016-04-04 2016-11-03 /pmc/articles/PMC5396462/ /pubmed/27041585 http://dx.doi.org/10.1038/onc.2016.81 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Yang, Xianzhi
Li, Xiaoxing
Zhang, Yanjie
Rodriguez-Rodriguez, Lorna
Xiang, Mengqing
Wang, Hui-Yun
Zheng, X.F. Steven
Rab1 in Cell Signaling, Cancer and Other Diseases
title Rab1 in Cell Signaling, Cancer and Other Diseases
title_full Rab1 in Cell Signaling, Cancer and Other Diseases
title_fullStr Rab1 in Cell Signaling, Cancer and Other Diseases
title_full_unstemmed Rab1 in Cell Signaling, Cancer and Other Diseases
title_short Rab1 in Cell Signaling, Cancer and Other Diseases
title_sort rab1 in cell signaling, cancer and other diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396462/
https://www.ncbi.nlm.nih.gov/pubmed/27041585
http://dx.doi.org/10.1038/onc.2016.81
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