TY - JOUR
T1 - Clinical utility of non-EpCAM based circulating tumor cell assays
AU - Austin, R. Garland
AU - Huang, Tony Jun
AU - Wu, Mengxi
AU - Armstrong, Andrew J.
AU - Zhang, Tian
N1 - Funding Information:
The authors acknowledge the academic environment at Duke University and the genitourinary oncology program that supported time and effort in preparing this manuscript. AJA received support from the Prostate Cancer Foundation Young Investigator Award. AJA and TZ report research funding from Janssen for circulating tumor cell biomarker studies.
Funding Information:
The authors acknowledge the academic environment at Duke University and the genitourinary oncology program that supported time and effort in preparing this manuscript. AJA received support from the Prostate Cancer Foundation . AJA and TZ report research funding from Janssen for circulating tumor cell biomarker studies.
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Methods enabling the isolation, detection, and characterization of circulating tumor cells (CTCs) in blood have clear potential to facilitate precision medicine approaches in patients with cancer, not only for prognostic purposes but also for prediction of the benefits of specific therapies in oncology. However, current CTC assays, which capture CTCs based on expression of epithelial cell adhesion molecule (EpCAM), fail to capture cells from de-differentiated tumors and carcinomas undergoing loss of the epithelial phenotype during the invasion/metastatic process. To address this limitation, many groups are developing non-EpCAM based CTC assays that incorporate nanotechnology to improve test sensitivity for rare but important cells that may otherwise go undetected, and therefore may improve upon clinical utility. In this review, we outline emerging non-EpCAM based CTC assays utilizing nanotechnology approaches for CTC capture or characterization, including dendrimers, magnetic nanoparticles, gold nanoparticles, negative selection chip or software-based on-slide methods, and nano-scale substrates. In addition, we address challenges that remain for the clinical translation of these platforms.
AB - Methods enabling the isolation, detection, and characterization of circulating tumor cells (CTCs) in blood have clear potential to facilitate precision medicine approaches in patients with cancer, not only for prognostic purposes but also for prediction of the benefits of specific therapies in oncology. However, current CTC assays, which capture CTCs based on expression of epithelial cell adhesion molecule (EpCAM), fail to capture cells from de-differentiated tumors and carcinomas undergoing loss of the epithelial phenotype during the invasion/metastatic process. To address this limitation, many groups are developing non-EpCAM based CTC assays that incorporate nanotechnology to improve test sensitivity for rare but important cells that may otherwise go undetected, and therefore may improve upon clinical utility. In this review, we outline emerging non-EpCAM based CTC assays utilizing nanotechnology approaches for CTC capture or characterization, including dendrimers, magnetic nanoparticles, gold nanoparticles, negative selection chip or software-based on-slide methods, and nano-scale substrates. In addition, we address challenges that remain for the clinical translation of these platforms.
KW - Biomarker
KW - Circulating tumor cell
KW - Liquid biopsy
KW - Nanotechnology
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U2 - 10.1016/j.addr.2018.01.013
DO - 10.1016/j.addr.2018.01.013
M3 - Review article
C2 - 29366804
AN - SCOPUS:85041701175
SN - 0169-409X
VL - 125
SP - 132
EP - 142
JO - Advanced Drug Delivery Reviews
JF - Advanced Drug Delivery Reviews
ER -