TY - JOUR
T1 - Generation of prostate cancer cell models of resistance to the anti-mitotic agent docetaxel
AU - Mohr, Lisa
AU - Carceles-Cordon, Marc
AU - Woo, Jungreem
AU - Cordon-Cardo, Carlos
AU - Domingo-Domenech, Josep
AU - Rodriguez-Bravo, Veronica
N1 - Funding Information:
V.R.-B. receives funding from the U.S. Department of Health & Human Services, NIH, National Cancer Institute grant number 1 K22 CA207458-01 and J.D.-D. receives funding from U.S. Department of Health & Human Services, NIH, National Cancer Institute grant number 1 R01 CA207311-01.
Publisher Copyright:
© 2017 Journal of Visualized Experiments.
PY - 2017/9/8
Y1 - 2017/9/8
N2 - Microtubule targeting agents (MTAs) are a mainstay in the treatment of a wide range of tumors. However, acquired resistance to chemotherapeutic drugs is a common mechanism of disease progression and a prognostic-determinant feature of malignant tumors. In prostate cancer (PC), resistance to MTAs such as the taxane Docetaxel dictates treatment failure as well as progression towards lethal stages of disease that are defined by a poor prognosis and high mortality rates. Though studied for decades, the array of mechanisms contributing to acquired resistance are not completely understood, and thus pose a significant limitation to the development of new therapeutic strategies that could benefit patients in these advanced stages of disease. In this protocol, we describe the generation of Docetaxel-resistant prostate cancer cell lines that mimic lethal features of late-stage prostate cancer, and therefore can be used to study the mechanisms by which acquired chemoresistance arises. Despite potential limitations intrinsic to a cell based model, such as the loss of resistance properties over time, the Docetaxel-resistant cell lines produced by this method have been successfully used in recent studies and offer the opportunity to advance our molecular understanding of acquired chemoresistance in lethal prostate cancer.
AB - Microtubule targeting agents (MTAs) are a mainstay in the treatment of a wide range of tumors. However, acquired resistance to chemotherapeutic drugs is a common mechanism of disease progression and a prognostic-determinant feature of malignant tumors. In prostate cancer (PC), resistance to MTAs such as the taxane Docetaxel dictates treatment failure as well as progression towards lethal stages of disease that are defined by a poor prognosis and high mortality rates. Though studied for decades, the array of mechanisms contributing to acquired resistance are not completely understood, and thus pose a significant limitation to the development of new therapeutic strategies that could benefit patients in these advanced stages of disease. In this protocol, we describe the generation of Docetaxel-resistant prostate cancer cell lines that mimic lethal features of late-stage prostate cancer, and therefore can be used to study the mechanisms by which acquired chemoresistance arises. Despite potential limitations intrinsic to a cell based model, such as the loss of resistance properties over time, the Docetaxel-resistant cell lines produced by this method have been successfully used in recent studies and offer the opportunity to advance our molecular understanding of acquired chemoresistance in lethal prostate cancer.
KW - Anti-mitotic Agents
KW - Cancer Research
KW - Chemotherapy Resistance
KW - Docetaxel
KW - Issue 127
KW - Microtubule Targeting Agents
KW - Prostate Cancer (PC)
KW - Taxanes
UR - http://www.scopus.com/inward/record.url?scp=85028975114&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85028975114&partnerID=8YFLogxK
U2 - 10.3791/56327
DO - 10.3791/56327
M3 - Article
C2 - 28930981
AN - SCOPUS:85028975114
SN - 1940-087X
VL - 2017
JO - Journal of visualized experiments : JoVE
JF - Journal of visualized experiments : JoVE
IS - 127
M1 - e56327
ER -