Article ; Online: The relationship between microRNAs and Rab family GTPases in human cancers.
Journal of cellular physiology
2019 Volume 234, Issue 8, Page(s) 12341–12352
Abstract: microRNAs (miRNAs), as a group of noncoding RNAs, posttranscriptionally control gene expression by binding to 3'-untranslated region (3'-UTR). Ras-associated binding (Rab) proteins function as molecular switches for regulating vesicular transport, which ... ...
Abstract | microRNAs (miRNAs), as a group of noncoding RNAs, posttranscriptionally control gene expression by binding to 3'-untranslated region (3'-UTR). Ras-associated binding (Rab) proteins function as molecular switches for regulating vesicular transport, which mainly have oncogenic roles in cancer development and preventing the efficacy of chemotherapies. Increased evidence supported that miRNAs/Rabs interaction have been determined as potential therapeutics for cancer therapy. Nevertheless, instability and cross-targeting of miRNAs are main limitations of using miRNA-based therapeutic. The mutual interplay between Rabs and miRNAs has been poorly understood. In the present review, we focused on the essence and activity of these molecules in cancer pathogenesis. Also, numerous hindrances and potential methods in the expansion of miRNA as an anticancer therapeutics are mentioned. |
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MeSH term(s) | 3' Untranslated Regions/genetics ; Gene Expression Regulation, Neoplastic/genetics ; Humans ; MicroRNAs/genetics ; Neoplasms/genetics ; Neoplasms/pathology ; Neoplasms/therapy ; Vesicular Transport Proteins/metabolism ; rab GTP-Binding Proteins/metabolism |
Chemical Substances | 3' Untranslated Regions ; MicroRNAs ; Vesicular Transport Proteins ; rab GTP-Binding Proteins (EC 3.6.5.2) |
Language | English |
Publishing date | 2019-01-04 |
Publishing country | United States |
Document type | Journal Article ; Review |
ZDB-ID | 3116-1 |
ISSN | 1097-4652 ; 0021-9541 |
ISSN (online) | 1097-4652 |
ISSN | 0021-9541 |
DOI | 10.1002/jcp.28038 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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