TY - JOUR
T1 - An update on synthetic high-density lipoprotein-like nanoparticles for cancer therapy
AU - Henrich, Stephen E.
AU - Thaxton, C. Shad
N1 - Funding Information:
CS Thaxton received funding from the Simpson Querrey Institute?s Center for Regenerative Nanomedicine at Northwestern University. SE Henrich received funding from the NIH with an NRSA individual graduate fellowship under Grant number 5 F30 CA225133-02. The authors are grateful to Michael Plebanek for assistance with graphic production.
Publisher Copyright:
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2019/6/3
Y1 - 2019/6/3
N2 - Introduction: Significant clinical correlations have been observed between serum high-density lipoprotein (HDL) cholesterol and cancer risk, outcomes, and patient response to specific treatments. While the biological processes underlying these correlations remain unclear, evidence suggests that HDLs actively inhibit tumor progression through a variety of mechanisms. As a result, synthetic HDLs have emerged as attractive agents for targeted cancer therapy. Areas covered: We present a focused review of recent developments in the use of synthetic HDLs for cancer therapy, including roles in drug delivery, RNAi, monotherapy, and immunotherapy. In addition to historic references relevant to the field, we searched the following databases for recent articles published from January 1st, 2015–May 1st, 2019: MEDLINE, Web of Science Core Collection, and Google Scholar. Expert opinion: Synthetic HDLs have already been used in human patients for cardiovascular disease, and have proven to be effective anticancer agents in pre-clinical testing, which should pave the way for future clinical trials in the setting of cancer. Given the growing notoriety of dysregulated cholesterol homeostasis as a key mechanism of cancer progression, and the immense success of synthetic HDLs in animal models, synthetic HDLs are well-poised to make significant strides toward the clinic as cancer therapy.
AB - Introduction: Significant clinical correlations have been observed between serum high-density lipoprotein (HDL) cholesterol and cancer risk, outcomes, and patient response to specific treatments. While the biological processes underlying these correlations remain unclear, evidence suggests that HDLs actively inhibit tumor progression through a variety of mechanisms. As a result, synthetic HDLs have emerged as attractive agents for targeted cancer therapy. Areas covered: We present a focused review of recent developments in the use of synthetic HDLs for cancer therapy, including roles in drug delivery, RNAi, monotherapy, and immunotherapy. In addition to historic references relevant to the field, we searched the following databases for recent articles published from January 1st, 2015–May 1st, 2019: MEDLINE, Web of Science Core Collection, and Google Scholar. Expert opinion: Synthetic HDLs have already been used in human patients for cardiovascular disease, and have proven to be effective anticancer agents in pre-clinical testing, which should pave the way for future clinical trials in the setting of cancer. Given the growing notoriety of dysregulated cholesterol homeostasis as a key mechanism of cancer progression, and the immense success of synthetic HDLs in animal models, synthetic HDLs are well-poised to make significant strides toward the clinic as cancer therapy.
KW - Cancer therapy
KW - cholesterol
KW - drug delivery
KW - high-density lipoprotein
KW - immunotherapy
KW - myeloid-derived suppressor cell
KW - nanoparticle
KW - siRNA
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U2 - 10.1080/14737140.2019.1624529
DO - 10.1080/14737140.2019.1624529
M3 - Review article
C2 - 31148521
AN - SCOPUS:85067209531
SN - 1473-7140
VL - 19
SP - 515
EP - 528
JO - Expert review of anticancer therapy
JF - Expert review of anticancer therapy
IS - 6
ER -