This video describes a protocol for generating taxane-resistant cell models of prostate cancer. These models can help study the pathways involved in progression to Docetaxel resistance in prostate cancer patients.
Protocol
1. Generation of Docetaxel-resistant Prostate Cancer Cells
NOTE: Perform cell treatments using Docetaxel solution stock used for the determination of IC50 drug concentration (prepare enough stock in advance for experimental use). Parental cells should be grown in parallel in a small flask throughout the whole procedure and exposed to vehicle (DMSO) in corresponding volumes mimicking the amounts used in the Docetaxel treated flasks.
Plate DU145 or 22Rv1 cells in 150 cm2 flasks containing 20 mL of media (3.5 x 106 cells per flask for DU145 and 6.5 x 106 cells per flask for 22Rv1). Use of 10 to 20 flasks of cells is recommended to have enough cells at the end of the protocol.
After 24 h, when cells are at about 70-80% confluence (Figure 1B, before Docetaxel), add Docetaxel at the IC50 concentration (5 nM for the cells described in this protocol).
After 72 h, aspirate drug-containing media and add fresh, Docetaxel-free media (Figure 1B, 72 h after Docetaxel). Change the media every 3-4 days. Within approximately 1-2 weeks, resistant clones will appear evident under the microscope (Figure 1B, 7 and 14 days after Docetaxel).
Aspirate media, carefully wash cells with 15 mL PBS and incubate with 4 mL 0.05% Trypsin-EDTA for 3-5 min at 37 °C to detach cells from the flask surface.
Resuspend trypsinized cells from the flask using 8 mL of fresh media. Pool cells from all treated flasks. Pellet cells by centrifugation (300 x g, 3 min, RT).
Remove the supernatant, resuspend the cell pellet in 20 mL of fresh media and plate the cells in 150 cm2 flasks (3.5 x 106 cells per flask for DU145 and 6.5 x 106 cells per flask for 22Rv1).
After 24 h, when cells are at about 70-80% confluence, add 5 nM Docetaxel (initial IC50 concentration) again.
Repeat steps 1.3 to 1.6 on day 3.
After 24 h, when cells are at about 70-80% confluence, treat them with 2X IC50 Docetaxel concentration (10 nM for the cells described in this protocol).
Repeat steps 1.3 to 1.8, following a dose-escalation of Docetaxel concentrations (25 nM, 50 nM, 100 nM, and 250 nM), to generate a stable population of cells growing in the flasks under the final highest concentration. For higher concentrations, the dose-escalation protocol can be implemented for up to 6 months until the 1,000 nM concentration is reached (Figure 2A).
Representative Results
Figure 1: Generation of Docetaxel-resistant prostate cancer cell model systems. (A) Diagram depicting the determination of the Docetaxel IC50 in the parental prostate cancer cell lines DU145 and 22Rv1 (Step 1 of the protocol). Expected percentages of cell viability and the Docetaxel dose-escalating concentrations needed are included. Representative DU145 and 22Rv1 cell viability graphs indicating 5 nM as the IC50 after 72 h of Docetaxel exposure are included. The experiments are triplicates and data represents the mean ± SD. (B) Representative bright-field microscopy images of DU145 and 22Rv1 cells at indicated times during the generation of Docetaxel resistance (Step 2 of the protocol). Red arrows indicate a Docetaxel resistant clone after the protocol is completed. Scale bars = 50 nm.
Figure 2: Timeline for the generation of Docetaxel-resistant prostate cancer cell models. (A) Representative diagram of the protocol timeline for generation of Docetaxel-resistant cell models. Illustration depicts the Docetaxel treatment, validation steps, and time needed for each part. (B) Schematic representation of the validation steps of the protocol including functional colony formation assays of parental and Docetaxel-resistant cells treated with the indicated Docetaxel concentrations for 72 h (in red), representative graph of colony percentage, and qRT-PCR for phenotypic validation.
開示
The authors have nothing to disclose.
Materials
DU145 cells
ATCC
HTB-81
22Rv1 cells
ATCC
CRL-2505
Docetaxel
Selleck Chemicals
S1148
in DMSO (10mM)
Tissue culture flask 150cm^{2}
Falcon
355001
RPMI 1640 Medium
Gibco
11875093
Supplemented with 10% FBS and
1% Penicilin/Streptomycin
Generating Chemoresistant Prostate Cancer Cells: A Procedure for Obtaining Drug-resistant Cancer Cells In Vitro. J. Vis. Exp. (Pending Publication), e20399, doi: (2023).