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Targeting SR-BI for Cancer Diagnostics, Imaging and Therapy

Scavenger receptor class B type I (SR-BI) plays an important role in trafficking cholesteryl esters between the core of high density lipoprotein and the liver. Interestingly, this integral membrane protein receptor is also implicated in the metabolism of cholesterol by cancer cells, whereby overexpr...

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Detalles Bibliográficos
Autores principales: Rajora, Maneesha A., Zheng, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037127/
https://www.ncbi.nlm.nih.gov/pubmed/27729859
http://dx.doi.org/10.3389/fphar.2016.00326
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author Rajora, Maneesha A.
Zheng, Gang
author_facet Rajora, Maneesha A.
Zheng, Gang
author_sort Rajora, Maneesha A.
collection PubMed
description Scavenger receptor class B type I (SR-BI) plays an important role in trafficking cholesteryl esters between the core of high density lipoprotein and the liver. Interestingly, this integral membrane protein receptor is also implicated in the metabolism of cholesterol by cancer cells, whereby overexpression of SR-BI has been observed in a number of tumors and cancer cell lines, including breast and prostate cancers. Consequently, SR-BI has recently gained attention as a cancer biomarker and exciting target for the direct cytosolic delivery of therapeutic agents. This brief review highlights these key developments in SR-BI-targeted cancer therapies and imaging probes. Special attention is given to the exploration of high density lipoprotein nanomimetic platforms that take advantage of upregulated SR-BI expression to facilitate targeted drug-delivery and cancer diagnostics, and promising future directions in the development of these agents.
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spelling pubmed-50371272016-10-11 Targeting SR-BI for Cancer Diagnostics, Imaging and Therapy Rajora, Maneesha A. Zheng, Gang Front Pharmacol Pharmacology Scavenger receptor class B type I (SR-BI) plays an important role in trafficking cholesteryl esters between the core of high density lipoprotein and the liver. Interestingly, this integral membrane protein receptor is also implicated in the metabolism of cholesterol by cancer cells, whereby overexpression of SR-BI has been observed in a number of tumors and cancer cell lines, including breast and prostate cancers. Consequently, SR-BI has recently gained attention as a cancer biomarker and exciting target for the direct cytosolic delivery of therapeutic agents. This brief review highlights these key developments in SR-BI-targeted cancer therapies and imaging probes. Special attention is given to the exploration of high density lipoprotein nanomimetic platforms that take advantage of upregulated SR-BI expression to facilitate targeted drug-delivery and cancer diagnostics, and promising future directions in the development of these agents. Frontiers Media S.A. 2016-09-27 /pmc/articles/PMC5037127/ /pubmed/27729859 http://dx.doi.org/10.3389/fphar.2016.00326 Text en Copyright © 2016 Rajora and Zheng. 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
Rajora, Maneesha A.
Zheng, Gang
Targeting SR-BI for Cancer Diagnostics, Imaging and Therapy
title Targeting SR-BI for Cancer Diagnostics, Imaging and Therapy
title_full Targeting SR-BI for Cancer Diagnostics, Imaging and Therapy
title_fullStr Targeting SR-BI for Cancer Diagnostics, Imaging and Therapy
title_full_unstemmed Targeting SR-BI for Cancer Diagnostics, Imaging and Therapy
title_short Targeting SR-BI for Cancer Diagnostics, Imaging and Therapy
title_sort targeting sr-bi for cancer diagnostics, imaging and therapy
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037127/
https://www.ncbi.nlm.nih.gov/pubmed/27729859
http://dx.doi.org/10.3389/fphar.2016.00326
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