Redox Regulation in Cancer Stem Cells

被引:92
作者
Ding, Shijie [1 ]
Li, Chunbao [1 ]
Cheng, Ninghui [2 ]
Cui, Xiaojiang [3 ,4 ]
Xu, Xinglian [1 ]
Zhou, Guanghong [1 ]
机构
[1] Nanjing Agr Univ, Coll Food Sci & Technol, Key Lab Meat Proc & Qual Control, Nanjing 210095, Jiangsu, Peoples R China
[2] Baylor Coll Med, USDA ARS, Children Nutr Res Ctr, Dept Pediat, Houston, TX 77030 USA
[3] Cedars Sinai Med Ctr, Samuel Oschin Comprehens Canc Inst, Womens Canc Program, Dept Surg, Los Angeles, CA 90048 USA
[4] Cedars Sinai Med Ctr, Samuel Oschin Comprehens Canc Inst, Womens Canc Program, Dept Obstet & Gynecol, Los Angeles, CA 90048 USA
基金
美国农业部; 美国国家卫生研究院;
关键词
NF-KAPPA-B; MYELOGENOUS LEUKEMIA STEM; OXIDATIVE STRESS; PROSTATE-CANCER; THIOREDOXIN REDUCTASE; TRANSCRIPTION FACTOR; ROS PRODUCTION; SELF-RENEWAL; TUMOR; NOTCH;
D O I
10.1155/2015/750798
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Reactive oxygen species (ROS) and ROS-dependent (redox regulation) signaling pathways and transcriptional activities are thought to be critical in stem cell self-renewal and differentiation during growth and organogenesis. Aberrant ROS burst and dysregulation of those ROS-dependent cellular processes are strongly associated with human diseases including many cancers. ROS levels are elevated in cancer cells partially due to their higher metabolism rate. In the past 15 years, the concept of cancer stem cells (CSCs) has been gaining ground as the subpopulation of cancer cells with stem cell-like properties and characteristics have been identified in various cancers. CSCs possess low levels of ROS and are responsible for cancer recurrence after chemotherapy or radiotherapy. Unfortunately, how CSCs control ROS production and scavenging and how ROS-dependent signaling pathways contribute to CSCs function remain poorly understood. This review focuses on the role of redox balance, especially in ROS-dependent cellular processes in cancer stem cells (CSCs). We updated recent advances in our understanding of ROS generation and elimination in CSCs and their effects on CSC self-renewal and differentiation through modulating signaling pathways and transcriptional activities. The review concludes that targeting CSCs by manipulating ROS metabolism/dependent pathways may be an effective approach for improving cancer treatment.
引用
收藏
页数:11
相关论文
共 141 条
[1]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[2]   Nrf2, a Cap'n'Collar transcription factor, regulates induction of the heme oxygenase-1 gene [J].
Alam, J ;
Stewart, D ;
Touchard, C ;
Boinapally, S ;
Choi, AMK ;
Cook, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (37) :26071-26078
[3]   Oxidants and Antioxidants in Breast Cancer [J].
Ambrosone, Christine B. .
ANTIOXIDANTS & REDOX SIGNALING, 2000, 2 (04) :903-918
[4]  
[Anonymous], MOL CARCINOGENESIS
[5]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[6]  
Bao B, 2014, CURR STEM CELL RES T, V9, P22
[7]   Astroglial NF-κB mediates oxidative stress by regulation of NADPH oxidase in a model of retinal ischemia reperfusion injury [J].
Barakat, David J. ;
Dvoriantchikova, Galina ;
Ivanov, Dmitry ;
Shestopalov, Valery I. .
JOURNAL OF NEUROCHEMISTRY, 2012, 120 (04) :586-597
[8]   Cigarette Smoke-induced Oxidative Stress A Role in Chronic Obstructive Pulmonary Disease Skeletal Muscle Dysfunction [J].
Barreiro, Esther ;
Peinado, Victor I. ;
Galdiz, Juan B. ;
Ferrer, Elisabet ;
Mann-Corral, Judith ;
Sanchez, Francisco ;
Gea, Joaquim ;
Albert Barbera, Joan .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2010, 182 (04) :477-488
[9]   PML inhibits HIF-1α translation and neoangiogenesis through repression of mTOR [J].
Bernardi, Rosa ;
Guernah, Ilhem ;
Jin, David ;
Grisendi, Silvia ;
Alimonti, Andrea ;
Teruya-Feldstein, Julie ;
Cordon-Cardo, Carlos ;
Simon, M. Celeste ;
Rafii, Shahin ;
Pandolfi, Pier Paolo .
NATURE, 2006, 442 (7104) :779-785
[10]  
Bonneau D, 2000, HUM MUTAT, V16, P109, DOI 10.1002/1098-1004(200008)16:2<109::AID-HUMU3>3.0.CO