The CTLH Complex in Cancer Cell Plasticity
Cancer cell plasticity is the ability of cancer cells to intermittently morph into different fittest phenotypic states. Due to the intrinsic capacity to change their composition and interactions, protein macromolecular complexes are the ideal instruments for transient transformation. This review foc...
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doaj-b7145e13e6584254b0f186d077aa21e12020-11-25T01:18:09ZengHindawi LimitedJournal of Oncology1687-84501687-84692019-01-01201910.1155/2019/42167504216750The CTLH Complex in Cancer Cell PlasticityNickelas Huffman0Dario Palmieri1Vincenzo Coppola2Department of Cancer Biology and Genetics, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio 43210, USADepartment of Cancer Biology and Genetics, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio 43210, USADepartment of Cancer Biology and Genetics, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio 43210, USACancer cell plasticity is the ability of cancer cells to intermittently morph into different fittest phenotypic states. Due to the intrinsic capacity to change their composition and interactions, protein macromolecular complexes are the ideal instruments for transient transformation. This review focuses on a poorly studied mammalian macromolecular complex called the CTLH (carboxy-terminal to LisH) complex. Currently, this macrostructure includes 11 known members (ARMC8, GID4, GID8, MAEA, MKLN1, RMND5A, RMND5B, RANBP9, RANBP10, WDR26, and YPEL5) and it has been shown to have E3-ligase enzymatic activity. CTLH proteins have been linked to all fundamental biological processes including proliferation, survival, programmed cell death, cell adhesion, and migration. At molecular level, the complex seems to interact and intertwine with key signaling pathways such as the PI3-kinase, WNT, TGFβ, and NFκB, which are key to cancer cell plasticity. As a whole, the CTLH complex is overexpressed in the most prevalent types of cancer and may hold the key to unlock many of the biological secrets that allow cancer cells to thrive in harsh conditions and resist antineoplastic therapy.http://dx.doi.org/10.1155/2019/4216750 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nickelas Huffman Dario Palmieri Vincenzo Coppola |
spellingShingle |
Nickelas Huffman Dario Palmieri Vincenzo Coppola The CTLH Complex in Cancer Cell Plasticity Journal of Oncology |
author_facet |
Nickelas Huffman Dario Palmieri Vincenzo Coppola |
author_sort |
Nickelas Huffman |
title |
The CTLH Complex in Cancer Cell Plasticity |
title_short |
The CTLH Complex in Cancer Cell Plasticity |
title_full |
The CTLH Complex in Cancer Cell Plasticity |
title_fullStr |
The CTLH Complex in Cancer Cell Plasticity |
title_full_unstemmed |
The CTLH Complex in Cancer Cell Plasticity |
title_sort |
ctlh complex in cancer cell plasticity |
publisher |
Hindawi Limited |
series |
Journal of Oncology |
issn |
1687-8450 1687-8469 |
publishDate |
2019-01-01 |
description |
Cancer cell plasticity is the ability of cancer cells to intermittently morph into different fittest phenotypic states. Due to the intrinsic capacity to change their composition and interactions, protein macromolecular complexes are the ideal instruments for transient transformation. This review focuses on a poorly studied mammalian macromolecular complex called the CTLH (carboxy-terminal to LisH) complex. Currently, this macrostructure includes 11 known members (ARMC8, GID4, GID8, MAEA, MKLN1, RMND5A, RMND5B, RANBP9, RANBP10, WDR26, and YPEL5) and it has been shown to have E3-ligase enzymatic activity. CTLH proteins have been linked to all fundamental biological processes including proliferation, survival, programmed cell death, cell adhesion, and migration. At molecular level, the complex seems to interact and intertwine with key signaling pathways such as the PI3-kinase, WNT, TGFβ, and NFκB, which are key to cancer cell plasticity. As a whole, the CTLH complex is overexpressed in the most prevalent types of cancer and may hold the key to unlock many of the biological secrets that allow cancer cells to thrive in harsh conditions and resist antineoplastic therapy. |
url |
http://dx.doi.org/10.1155/2019/4216750 |
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