Friend or Foe: Regulation, Downstream Effectors of RRAD in Cancer

Ras-related associated with diabetes (RRAD), a member of the Ras-related GTPase superfamily, is primarily a cytosolic protein that actives in the plasma membrane. RRAD is highly expressed in type 2 diabetes patients and as a biomarker of congestive heart failure. Mounting evidence showed that RRAD i...

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Main Authors: Zhangyue Sun, Yongkang Li, Xiaolu Tan, Wanyi Liu, Xinglin He, Deyuan Pan, Enmin Li, Liyan Xu, Lin Long
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:Biomolecules
Subjects:
Online Access:https://www.mdpi.com/2218-273X/13/3/477
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author Zhangyue Sun
Yongkang Li
Xiaolu Tan
Wanyi Liu
Xinglin He
Deyuan Pan
Enmin Li
Liyan Xu
Lin Long
author_facet Zhangyue Sun
Yongkang Li
Xiaolu Tan
Wanyi Liu
Xinglin He
Deyuan Pan
Enmin Li
Liyan Xu
Lin Long
author_sort Zhangyue Sun
collection DOAJ
description Ras-related associated with diabetes (RRAD), a member of the Ras-related GTPase superfamily, is primarily a cytosolic protein that actives in the plasma membrane. RRAD is highly expressed in type 2 diabetes patients and as a biomarker of congestive heart failure. Mounting evidence showed that RRAD is important for the progression and metastasis of tumor cells, which play opposite roles as an oncogene or tumor suppressor gene depending on cancer and cell type. These findings are of great significance, especially given that relevant molecular mechanisms are being discovered. Being regulated in various pathways, RRAD plays wide spectrum cellular activity including tumor cell division, motility, apoptosis, and energy metabolism by modulating tumor-related gene expression and interacting with multiple downstream effectors. Additionally, RRAD in senescence may contribute to its role in cancer. Despite the twofold characters of RRAD, targeted therapies are becoming a potential therapeutic strategy to combat cancers. This review will discuss the dual identity of RRAD in specific cancer type, provides an overview of the regulation and downstream effectors of RRAD to offer valuable insights for readers, explore the intracellular role of RRAD in cancer, and give a reference for future mechanistic studies.
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spelling doaj.art-4ee7af06a5a641d39ad1b9ff4fb6c9dd2023-11-17T09:51:51ZengMDPI AGBiomolecules2218-273X2023-03-0113347710.3390/biom13030477Friend or Foe: Regulation, Downstream Effectors of RRAD in CancerZhangyue Sun0Yongkang Li1Xiaolu Tan2Wanyi Liu3Xinglin He4Deyuan Pan5Enmin Li6Liyan Xu7Lin Long8Department of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou 515041, ChinaDepartment of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou 515041, ChinaDepartment of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou 515041, ChinaDepartment of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou 515041, ChinaDepartment of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou 515041, ChinaDepartment of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou 515041, ChinaDepartment of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou 515041, ChinaDepartment of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou 515041, ChinaDepartment of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou 515041, ChinaRas-related associated with diabetes (RRAD), a member of the Ras-related GTPase superfamily, is primarily a cytosolic protein that actives in the plasma membrane. RRAD is highly expressed in type 2 diabetes patients and as a biomarker of congestive heart failure. Mounting evidence showed that RRAD is important for the progression and metastasis of tumor cells, which play opposite roles as an oncogene or tumor suppressor gene depending on cancer and cell type. These findings are of great significance, especially given that relevant molecular mechanisms are being discovered. Being regulated in various pathways, RRAD plays wide spectrum cellular activity including tumor cell division, motility, apoptosis, and energy metabolism by modulating tumor-related gene expression and interacting with multiple downstream effectors. Additionally, RRAD in senescence may contribute to its role in cancer. Despite the twofold characters of RRAD, targeted therapies are becoming a potential therapeutic strategy to combat cancers. This review will discuss the dual identity of RRAD in specific cancer type, provides an overview of the regulation and downstream effectors of RRAD to offer valuable insights for readers, explore the intracellular role of RRAD in cancer, and give a reference for future mechanistic studies.https://www.mdpi.com/2218-273X/13/3/477RRADdual identityregulationdownstream effectorscancer
spellingShingle Zhangyue Sun
Yongkang Li
Xiaolu Tan
Wanyi Liu
Xinglin He
Deyuan Pan
Enmin Li
Liyan Xu
Lin Long
Friend or Foe: Regulation, Downstream Effectors of RRAD in Cancer
Biomolecules
RRAD
dual identity
regulation
downstream effectors
cancer
title Friend or Foe: Regulation, Downstream Effectors of RRAD in Cancer
title_full Friend or Foe: Regulation, Downstream Effectors of RRAD in Cancer
title_fullStr Friend or Foe: Regulation, Downstream Effectors of RRAD in Cancer
title_full_unstemmed Friend or Foe: Regulation, Downstream Effectors of RRAD in Cancer
title_short Friend or Foe: Regulation, Downstream Effectors of RRAD in Cancer
title_sort friend or foe regulation downstream effectors of rrad in cancer
topic RRAD
dual identity
regulation
downstream effectors
cancer
url https://www.mdpi.com/2218-273X/13/3/477
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AT xinglinhe friendorfoeregulationdownstreameffectorsofrradincancer
AT deyuanpan friendorfoeregulationdownstreameffectorsofrradincancer
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