Antibodies targeting cancer stem cells A new paradigm in immunotherapy?

被引:140
作者
Deonarain, Mahendra P. [1 ]
Kousparou, Christina A. [2 ]
Epenetos, Agamemnon A. [1 ,2 ,3 ,4 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Div Cell & Mol Biol, Dept Life Sci, London SW7 2AZ, England
[2] Bank Cyprus Oncol Ctr, Trojantec Ltd, Nicosia, Cyprus
[3] Access Pharmaceut Inc, London, England
[4] Harley St Oncol Clin, London, England
基金
英国惠康基金;
关键词
antibody; targeting; cancer; stem cell; therapy; ACUTE MYELOID-LEUKEMIA; HUMANIZED MONOCLONAL-ANTIBODY; GROWTH-FACTOR RECEPTOR; PROSTATE-CANCER; BREAST-CANCER; TUMOR-GROWTH; PANCREATIC-CANCER; COLON-CANCER; IN-VIVO; ADHESION MOLECULES;
D O I
10.4161/mabs.1.1.7347
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Antibody targeting of cancer is showing clinical and commercial success after much intense research and development over the last 30 years. They still have the potential to delivery long-term cures but a shift in thinking towards a cancer stem cell (CSC) model for tumor development is certain to impact on how antibodies are selected and developed, the targets they bind to and the drugs used in combination with them. CSCs have been identified from many human tumors and share many of the characteristics of normal stem cells. The ability to renew, metabolically or physically protect themselves from xenobiotics and DNA damage and the range of locomotory-related receptors expressed could explain the observations of drug resistance and radiation insensitivity leading to metastasis and patient relapse. Targeting CSCs could be a strategy to improve the outcome of cancer therapy but this is not as simple as it seems. Targets such as CD133 and EpCAM/ESA could mark out CSCs from normal cells enabling specific intervention but indirect strategies such as interfering with the establishment of a supportive niche through anti-angiogenic or anti-stroma therapy could be more effective. This review will outline the recent discoveries for CSCs across the major tumor types highlighting the possible molecules for intervention. Examples of antibody-directed CSC therapies and the outlook for the future development of this emerging area will be given.
引用
收藏
页码:12 / 25
页数:14
相关论文
共 177 条
[1]
Abraham BK, 2005, CLIN CANCER RES, V11, P1154
[2]
The chemokine SDF-1 is a chemoattractant for human CD34(+) hematopoietic progenitor cells and provides a new mechanism to explain the mobilization of CD34(+) progenitors to peripheral blood [J].
Aiuti, A ;
Webb, IJ ;
Bleul, C ;
Springer, T ;
GutierrezRamos, JC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (01) :111-120
[3]
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
[4]
Mechanisms of regulation of CXCR4/SDF-1 (CXCL12)-dependent migration and homing in multiple myeloma [J].
Alsayed, Yazan ;
Ngo, Hai ;
Runnels, Judith ;
Leleu, Xavier ;
Singha, Ujjal K. ;
Pitsillides, Costas M. ;
Spencer, Joel A. ;
Kimlinger, Teresa ;
Ghobrial, Joanna M. ;
Jia, Xiaoying ;
Lu, Ganwei ;
Timm, Michael ;
Kumar, Ashok ;
Cote, Daniel ;
Veilleux, Israel ;
Hedin, Karen E. ;
Roodman, G. David ;
WitZig, Thomas E. ;
Kung, Andrew L. ;
Hideshima, Teru ;
Anderson, Kenneth C. ;
Lin, Charles P. ;
Ghobrial, Irene M. .
BLOOD, 2007, 109 (07) :2708-2717
[5]
In vitro and in vivo pharmacology and pharmacokinetics of a Human Engineered™ monoclonal antibody to epithelial cell adhesion molecule [J].
Ammons, WS ;
Bauer, RJ ;
Horwitz, AH ;
Chen, ZJ ;
Bautista, E ;
Ruan, HH ;
Abramova, M ;
Scott, KR ;
Dedrick, RL .
NEOPLASIA, 2003, 5 (02) :146-154
[6]
Recombinant protein expression for therapeutic applications [J].
Andersen, DC ;
Krummen, L .
CURRENT OPINION IN BIOTECHNOLOGY, 2002, 13 (02) :117-123
[7]
Antibody-directed enzyme prodrug therapy (ADEPT) for cancer [J].
Bagshawe, KD ;
Sharma, SK ;
Begent, RHJ .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2004, 4 (11) :1777-1789
[8]
The biology of the 17-1A antigen (Ep-CAM) [J].
Balzar, M ;
Winter, MJ ;
de Boer, CJ ;
Litvinov, SV .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1999, 77 (10) :699-712
[9]
Targeting cancer stem cells through L1CAM suppresses glioma growth [J].
Bao, Shideng ;
Wu, Qiulian ;
Li, Zhizhong ;
Sathornsumetee, Sith ;
Wang, Hui ;
McLendon, Roger E. ;
Hjehneland, Anita B. ;
Rich, Jeremy N. .
CANCER RESEARCH, 2008, 68 (15) :6043-6048
[10]
Glioma stem cells promote radioresistance by preferential activation of the DNA damage response [J].
Bao, Shideng ;
Wu, Qiulian ;
McLendon, Roger E. ;
Hao, Yueling ;
Shi, Qing ;
Hjelmeland, Anita B. ;
Dewhirst, Mark W. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
NATURE, 2006, 444 (7120) :756-760