Epithelial protein lost in neoplasm (EPLIN): Beyond a tumor suppressor

The majority of cancer-related deaths are caused by tumor recurrence, metastasis and therapeutic resistance. During the late stages of tumor progression, multiple factors are involved, including the downregulation and/or loss of function of metastasis suppressors. Epithelial protein lost in neoplasm...

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Main Author: Daqing Wu
Format: Article
Language:English
Published: KeAi Communications Co., Ltd. 2017-06-01
Series:Genes and Diseases
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2352304217300259
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author Daqing Wu
author_facet Daqing Wu
author_sort Daqing Wu
collection DOAJ
description The majority of cancer-related deaths are caused by tumor recurrence, metastasis and therapeutic resistance. During the late stages of tumor progression, multiple factors are involved, including the downregulation and/or loss of function of metastasis suppressors. Epithelial protein lost in neoplasm (EPLIN), an actin-binding protein, was initially identified as a putative tumor suppressor that is frequently downregulated in epithelial tumors. Recent evidence indicates that EPLIN may negatively regulate epithelia-to-mesenchymal transition (EMT), a crucial process by which cancer cells acquire invasive capabilities and therapeutic resistance. Importantly, downregulation of EPLIN is associated with clinical metastasis in a variety of solid tumors, suggesting that EPLIN could be a suppressor of metastasis. In this review, I will discuss the regulation and function of EPLIN in human cancer cells and explore the clinical significance of EPLIN in metastatic disease.
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spelling doaj.art-9986ffd490164830b14e9fc873ec11e72023-09-02T15:15:13ZengKeAi Communications Co., Ltd.Genes and Diseases2352-30422017-06-014210010710.1016/j.gendis.2017.03.002Epithelial protein lost in neoplasm (EPLIN): Beyond a tumor suppressorDaqing Wu0Georgia Cancer Center and Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta University, Augusta, GA, USAThe majority of cancer-related deaths are caused by tumor recurrence, metastasis and therapeutic resistance. During the late stages of tumor progression, multiple factors are involved, including the downregulation and/or loss of function of metastasis suppressors. Epithelial protein lost in neoplasm (EPLIN), an actin-binding protein, was initially identified as a putative tumor suppressor that is frequently downregulated in epithelial tumors. Recent evidence indicates that EPLIN may negatively regulate epithelia-to-mesenchymal transition (EMT), a crucial process by which cancer cells acquire invasive capabilities and therapeutic resistance. Importantly, downregulation of EPLIN is associated with clinical metastasis in a variety of solid tumors, suggesting that EPLIN could be a suppressor of metastasis. In this review, I will discuss the regulation and function of EPLIN in human cancer cells and explore the clinical significance of EPLIN in metastatic disease.http://www.sciencedirect.com/science/article/pii/S2352304217300259Actin cytoskeletonChemoresistanceEpithelial-to-mesenchymal transitionEPLINMetastasis suppressorTumor suppressor
spellingShingle Daqing Wu
Epithelial protein lost in neoplasm (EPLIN): Beyond a tumor suppressor
Genes and Diseases
Actin cytoskeleton
Chemoresistance
Epithelial-to-mesenchymal transition
EPLIN
Metastasis suppressor
Tumor suppressor
title Epithelial protein lost in neoplasm (EPLIN): Beyond a tumor suppressor
title_full Epithelial protein lost in neoplasm (EPLIN): Beyond a tumor suppressor
title_fullStr Epithelial protein lost in neoplasm (EPLIN): Beyond a tumor suppressor
title_full_unstemmed Epithelial protein lost in neoplasm (EPLIN): Beyond a tumor suppressor
title_short Epithelial protein lost in neoplasm (EPLIN): Beyond a tumor suppressor
title_sort epithelial protein lost in neoplasm eplin beyond a tumor suppressor
topic Actin cytoskeleton
Chemoresistance
Epithelial-to-mesenchymal transition
EPLIN
Metastasis suppressor
Tumor suppressor
url http://www.sciencedirect.com/science/article/pii/S2352304217300259
work_keys_str_mv AT daqingwu epithelialproteinlostinneoplasmeplinbeyondatumorsuppressor