TY - CHAP
T1 - Targeting Cancer Stem Cells-Modulating Embryonic Stem Cell Signaling, Epigenetics, and Tumor Metabolism
AU - Takebe, Naoko
AU - Harris, Pamela Jo
AU - Kondo, Yutaka
AU - Nair, Abhilasha
AU - Percy Ivy, S.
AU - Saya, Hideyuki
N1 - Publisher Copyright:
© 2014 by John Wiley & Sons, Inc. All rights reserved.
PY - 2014/4/14
Y1 - 2014/4/14
N2 - Cancer stem cells (CSC) are important to understand in order to develop solutions to treat tumor metastasis and resistance to therapy. CSCs are characterized by their ability to self-renew and differentiate into tumors, ultimately leading to therapeutic resistance. This chapter summarizes the various potential therapeutic approaches to control CSCs survival and proliferation based on preclinical and clinical study-based rationale. The proposed agents range from investigational, which are still in pre-clinical stage, already in early clinical investigational stage, or already approved for clinical use for other indications. The manuscript covers the agents targeting embryonic stem cell signaling, epigenetic control, cancer metabolism, and induction of epithelial-to-mesenchymal transition (EMT). The combination of therapeutic strategies to reduce bulk tumor populations and to target CSCs population may provide clinically meaningful tumor suppression. The development of new anti-CSC therapeutic agents and the complexity of potential molecular pathways controlling CSC survival are described in this review.
AB - Cancer stem cells (CSC) are important to understand in order to develop solutions to treat tumor metastasis and resistance to therapy. CSCs are characterized by their ability to self-renew and differentiate into tumors, ultimately leading to therapeutic resistance. This chapter summarizes the various potential therapeutic approaches to control CSCs survival and proliferation based on preclinical and clinical study-based rationale. The proposed agents range from investigational, which are still in pre-clinical stage, already in early clinical investigational stage, or already approved for clinical use for other indications. The manuscript covers the agents targeting embryonic stem cell signaling, epigenetic control, cancer metabolism, and induction of epithelial-to-mesenchymal transition (EMT). The combination of therapeutic strategies to reduce bulk tumor populations and to target CSCs population may provide clinically meaningful tumor suppression. The development of new anti-CSC therapeutic agents and the complexity of potential molecular pathways controlling CSC survival are described in this review.
KW - CSC therapeutic targets
KW - Cancer stem cells (CSCs)
KW - Embryonic stem cell signaling
KW - Epigenetics
KW - Epithelial-to-mesenchymal transition (EMT)
KW - Hedgehog signaling pathway
KW - Notch signaling pathway
KW - Polycomb-repressive complexes
KW - Tumor metabolism
KW - Wnt signaling pathway
UR - http://www.scopus.com/inward/record.url?scp=84926475250&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84926475250&partnerID=8YFLogxK
U2 - 10.1002/9781118356203.ch23
DO - 10.1002/9781118356203.ch23
M3 - Chapter
AN - SCOPUS:84926475250
SN - 9781118356166
SP - 295
EP - 317
BT - Cancer Stem Cells
PB - Wiley Blackwell
ER -