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Apolipoprotein A-I and Cancer

High-density lipoprotein (HDL) and apolipoprotein A-I (apoA-I), the predominant protein in plasma HDL, have long been the focus of intense studies in the field of atherosclerosis and cardiovascular disease. ApoA-I, in large part, is responsible for HDL assembly and its main atheroprotective function...

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Autores principales: Zamanian-Daryoush, Maryam, DiDonato, Joseph A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642354/
https://www.ncbi.nlm.nih.gov/pubmed/26617517
http://dx.doi.org/10.3389/fphar.2015.00265
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author Zamanian-Daryoush, Maryam
DiDonato, Joseph A.
author_facet Zamanian-Daryoush, Maryam
DiDonato, Joseph A.
author_sort Zamanian-Daryoush, Maryam
collection PubMed
description High-density lipoprotein (HDL) and apolipoprotein A-I (apoA-I), the predominant protein in plasma HDL, have long been the focus of intense studies in the field of atherosclerosis and cardiovascular disease. ApoA-I, in large part, is responsible for HDL assembly and its main atheroprotective function, that of shuttling excess cholesterol from peripheral tissues to the liver for excretion (reverse cholesterol transport). Recently, a protective role for HDL in cancer was suggested from several large clinical studies where an inverse relationship between plasma HDL-cholesterol (HDL-C) levels and risk of developing cancer was noted. This notion has now been tested and found to be supported in mouse tumor studies, where increasing levels of apoA-I/HDL were discovered to protect against tumor development and provision of human apoA-I was therapeutic against established tumors. This mini-review discusses the emerging role of apoA-I in tumor biology and its potential as cancer therapeutic.
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spelling pubmed-46423542015-11-27 Apolipoprotein A-I and Cancer Zamanian-Daryoush, Maryam DiDonato, Joseph A. Front Pharmacol Pharmacology High-density lipoprotein (HDL) and apolipoprotein A-I (apoA-I), the predominant protein in plasma HDL, have long been the focus of intense studies in the field of atherosclerosis and cardiovascular disease. ApoA-I, in large part, is responsible for HDL assembly and its main atheroprotective function, that of shuttling excess cholesterol from peripheral tissues to the liver for excretion (reverse cholesterol transport). Recently, a protective role for HDL in cancer was suggested from several large clinical studies where an inverse relationship between plasma HDL-cholesterol (HDL-C) levels and risk of developing cancer was noted. This notion has now been tested and found to be supported in mouse tumor studies, where increasing levels of apoA-I/HDL were discovered to protect against tumor development and provision of human apoA-I was therapeutic against established tumors. This mini-review discusses the emerging role of apoA-I in tumor biology and its potential as cancer therapeutic. Frontiers Media S.A. 2015-11-12 /pmc/articles/PMC4642354/ /pubmed/26617517 http://dx.doi.org/10.3389/fphar.2015.00265 Text en Copyright © 2015 Zamanian-Daryoush and DiDonato. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Zamanian-Daryoush, Maryam
DiDonato, Joseph A.
Apolipoprotein A-I and Cancer
title Apolipoprotein A-I and Cancer
title_full Apolipoprotein A-I and Cancer
title_fullStr Apolipoprotein A-I and Cancer
title_full_unstemmed Apolipoprotein A-I and Cancer
title_short Apolipoprotein A-I and Cancer
title_sort apolipoprotein a-i and cancer
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642354/
https://www.ncbi.nlm.nih.gov/pubmed/26617517
http://dx.doi.org/10.3389/fphar.2015.00265
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