TY - JOUR
T1 - Isolation and characterization of tumor-initiating cells from sarcoma patient-derived xenografts
AU - Han, Dan
AU - Rodriguez-Bravo, Veronica
AU - Izadmehr, Sudeh
AU - Domingo-Domenech, Josep
AU - Cordon-Cardo, Carlos
N1 - Funding Information:
This research was supported by NCI-P01-CA087497 (to C.C.-C. and D.H.) and NIH-U 54-0OD020353 (to C.C.-C., D.H., and J.D.-D.), the Agilent Thought Leader Award (to C.C.-C.), and the Martel Foundation (to C.C.-C. and J.D.-D.).
Publisher Copyright:
© 2019 Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.
PY - 2019/6
Y1 - 2019/6
N2 - The existence and importance of tumor-initiating cells (TICs) have been supported by increasing evidence during the past decade. These TICs have been shown to be responsible for tumor initiation, metastasis, and drug resistance. Therefore, it is important to develop specific TIC-targeting therapy in addition to current chemotherapy strategies, which mostly focus on the bulk of non-TICs. In order to further understand the mechanism behind the malignancy of TICs, we describe a method to isolate and to characterize TICs in human sarcomas. Herein, we show a detailed protocol to generate patient-derived xenografts (PDXs) of human sarcomas and to isolate TICs by fluorescence-activated cell sorting (FACS) using human leukocyte antigen class I (HLA-1) as a negative marker. Also, we describe how to functionally characterize these TICs, including a sphere formation assay and a tumor formation assay, and to induce differentiation along mesenchymal pathways. The isolation and characterization of PDX TICs provide clues for the discovery of potential targeting therapy reagents. Moreover, increasing evidence suggests that this protocol may be further extended to isolate and characterize TICs from other types of human cancers.
AB - The existence and importance of tumor-initiating cells (TICs) have been supported by increasing evidence during the past decade. These TICs have been shown to be responsible for tumor initiation, metastasis, and drug resistance. Therefore, it is important to develop specific TIC-targeting therapy in addition to current chemotherapy strategies, which mostly focus on the bulk of non-TICs. In order to further understand the mechanism behind the malignancy of TICs, we describe a method to isolate and to characterize TICs in human sarcomas. Herein, we show a detailed protocol to generate patient-derived xenografts (PDXs) of human sarcomas and to isolate TICs by fluorescence-activated cell sorting (FACS) using human leukocyte antigen class I (HLA-1) as a negative marker. Also, we describe how to functionally characterize these TICs, including a sphere formation assay and a tumor formation assay, and to induce differentiation along mesenchymal pathways. The isolation and characterization of PDX TICs provide clues for the discovery of potential targeting therapy reagents. Moreover, increasing evidence suggests that this protocol may be further extended to isolate and characterize TICs from other types of human cancers.
KW - Cancer research
KW - Human leukocyte antigen-1
KW - Human tissue samples
KW - Intratumoral heterogeneity
KW - Issue 148
KW - Patient-derived xenograft
KW - Sarcomas
KW - Tumor-initiating cells
UR - http://www.scopus.com/inward/record.url?scp=85068969003&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85068969003&partnerID=8YFLogxK
U2 - 10.3791/57011
DO - 10.3791/57011
M3 - Article
C2 - 31259909
AN - SCOPUS:85068969003
SN - 1940-087X
VL - 2019
JO - Journal of visualized experiments : JoVE
JF - Journal of visualized experiments : JoVE
IS - 148
M1 - e57011
ER -