TY - JOUR
T1 - Cancer stem cells in neuroblastoma therapy resistance
AU - Aravindan, Natarajan
AU - Jain, Drishti
AU - Somasundaram, Dinesh Babu
AU - Herman, Terence S.
AU - Aravindan, Sheeja
N1 - Funding Information:
The authors are supported by the research funding from the National Institutes of Health (NIH 1P20GM103639-01) from the COBRE Program of NIH; OUHSC Department of Radiation Oncology Research Development Funds.
Publisher Copyright:
© The Author(s) 2019.
PY - 2019
Y1 - 2019
N2 - Neuroblastoma (NB) is the most common cancer of infancy and accounts for nearly one tenth of pediatric cancer deaths. This mortality rate has been attributed to the > 50% frequency of relapse despite intensive, multimodal clinical therapy in patients with progressive NB. Given the disease’s heterogeneity and developed resistance, attaining a cure after relapse of progressive NB is highly challenging. A rapid decrease in the timeline between successive recurrences is likely due to the ongoing acquisition of genetic rearrangements in undifferentiated NB-cancer stem cells (CSCs). In this review, we present the current understanding of NB-CSCs, their intrinsic role in tumorigenesis, their function in disease progression, and their influence on acquired therapy resistance and tumor evolution. In particular, this review focus on the intrinsic involvement of stem cells and signaling in the genesis of NB, the function of pre-existing CSCs in NB progression and therapy response, the formation and influence of induced CSCs (iCSCs) in drug resistance and tumor evolution, and the development of a CSC-targeted therapeutic approach.
AB - Neuroblastoma (NB) is the most common cancer of infancy and accounts for nearly one tenth of pediatric cancer deaths. This mortality rate has been attributed to the > 50% frequency of relapse despite intensive, multimodal clinical therapy in patients with progressive NB. Given the disease’s heterogeneity and developed resistance, attaining a cure after relapse of progressive NB is highly challenging. A rapid decrease in the timeline between successive recurrences is likely due to the ongoing acquisition of genetic rearrangements in undifferentiated NB-cancer stem cells (CSCs). In this review, we present the current understanding of NB-CSCs, their intrinsic role in tumorigenesis, their function in disease progression, and their influence on acquired therapy resistance and tumor evolution. In particular, this review focus on the intrinsic involvement of stem cells and signaling in the genesis of NB, the function of pre-existing CSCs in NB progression and therapy response, the formation and influence of induced CSCs (iCSCs) in drug resistance and tumor evolution, and the development of a CSC-targeted therapeutic approach.
KW - Cancer stem cells
KW - Clonal selection
KW - Drug resistance
KW - Induced cancer stem cell
KW - Neuroblastoma
KW - Therapy resistance
UR - http://www.scopus.com/inward/record.url?scp=85079894314&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85079894314&partnerID=8YFLogxK
U2 - 10.20517/cdr.2019.72
DO - 10.20517/cdr.2019.72
M3 - Review article
AN - SCOPUS:85079894314
SN - 2578-532X
VL - 2
SP - 948
EP - 967
JO - Cancer Drug Resistance
JF - Cancer Drug Resistance
IS - 4
ER -