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Targeting the SR-B1 Receptor as a Gateway for Cancer Therapy and Imaging

Malignant tumors display remarkable heterogeneity to the extent that even at the same tissue site different types of cells with varying genetic background may be found. In contrast, a relatively consistent marker the scavenger receptor type B1 (SR-B1) has been found to be consistently overexpressed...

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Autores principales: Mooberry, Linda K., Sabnis, Nirupama A., Panchoo, Marlyn, Nagarajan, Bhavani, Lacko, Andras G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5156841/
https://www.ncbi.nlm.nih.gov/pubmed/28018216
http://dx.doi.org/10.3389/fphar.2016.00466
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author Mooberry, Linda K.
Sabnis, Nirupama A.
Panchoo, Marlyn
Nagarajan, Bhavani
Lacko, Andras G.
author_facet Mooberry, Linda K.
Sabnis, Nirupama A.
Panchoo, Marlyn
Nagarajan, Bhavani
Lacko, Andras G.
author_sort Mooberry, Linda K.
collection PubMed
description Malignant tumors display remarkable heterogeneity to the extent that even at the same tissue site different types of cells with varying genetic background may be found. In contrast, a relatively consistent marker the scavenger receptor type B1 (SR-B1) has been found to be consistently overexpressed by most tumor cells. Scavenger Receptor Class B Type I (SR-BI) is a high density lipoprotein (HDL) receptor that facilitates the uptake of cholesterol esters from circulating lipoproteins. Additional findings suggest a critical role for SR-BI in cholesterol metabolism, signaling, motility, and proliferation of cancer cells and thus a potential major impact in carcinogenesis and metastasis. Recent findings indicate that the level of SR-BI expression correlate with aggressiveness and poor survival in breast and prostate cancer. Moreover, genomic data show that depending on the type of cancer, high or low SR-BI expression may promote poor survival. This review discusses the importance of SR-BI as a diagnostic as well as prognostic indicator of cancer to help elucidate the contributions of this protein to cancer development, progression, and survival. In addition, the SR-B1 receptor has been shown to serve as a potential gateway for the delivery of therapeutic agents when reconstituted high density lipoprotein nanoparticles are used for their transport to cancer cells and tumors. Opportunities for the development of new technologies, particularly in the areas of cancer therapy and tumor imaging are discussed.
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spelling pubmed-51568412016-12-23 Targeting the SR-B1 Receptor as a Gateway for Cancer Therapy and Imaging Mooberry, Linda K. Sabnis, Nirupama A. Panchoo, Marlyn Nagarajan, Bhavani Lacko, Andras G. Front Pharmacol Pharmacology Malignant tumors display remarkable heterogeneity to the extent that even at the same tissue site different types of cells with varying genetic background may be found. In contrast, a relatively consistent marker the scavenger receptor type B1 (SR-B1) has been found to be consistently overexpressed by most tumor cells. Scavenger Receptor Class B Type I (SR-BI) is a high density lipoprotein (HDL) receptor that facilitates the uptake of cholesterol esters from circulating lipoproteins. Additional findings suggest a critical role for SR-BI in cholesterol metabolism, signaling, motility, and proliferation of cancer cells and thus a potential major impact in carcinogenesis and metastasis. Recent findings indicate that the level of SR-BI expression correlate with aggressiveness and poor survival in breast and prostate cancer. Moreover, genomic data show that depending on the type of cancer, high or low SR-BI expression may promote poor survival. This review discusses the importance of SR-BI as a diagnostic as well as prognostic indicator of cancer to help elucidate the contributions of this protein to cancer development, progression, and survival. In addition, the SR-B1 receptor has been shown to serve as a potential gateway for the delivery of therapeutic agents when reconstituted high density lipoprotein nanoparticles are used for their transport to cancer cells and tumors. Opportunities for the development of new technologies, particularly in the areas of cancer therapy and tumor imaging are discussed. Frontiers Media S.A. 2016-12-15 /pmc/articles/PMC5156841/ /pubmed/28018216 http://dx.doi.org/10.3389/fphar.2016.00466 Text en Copyright © 2016 Mooberry, Sabnis, Panchoo, Nagarajan and Lacko. 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
Mooberry, Linda K.
Sabnis, Nirupama A.
Panchoo, Marlyn
Nagarajan, Bhavani
Lacko, Andras G.
Targeting the SR-B1 Receptor as a Gateway for Cancer Therapy and Imaging
title Targeting the SR-B1 Receptor as a Gateway for Cancer Therapy and Imaging
title_full Targeting the SR-B1 Receptor as a Gateway for Cancer Therapy and Imaging
title_fullStr Targeting the SR-B1 Receptor as a Gateway for Cancer Therapy and Imaging
title_full_unstemmed Targeting the SR-B1 Receptor as a Gateway for Cancer Therapy and Imaging
title_short Targeting the SR-B1 Receptor as a Gateway for Cancer Therapy and Imaging
title_sort targeting the sr-b1 receptor as a gateway for cancer therapy and imaging
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5156841/
https://www.ncbi.nlm.nih.gov/pubmed/28018216
http://dx.doi.org/10.3389/fphar.2016.00466
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