Therapeutic stem-cells for cancer treatment: hopes and hurdles in tactical warfare

被引:132
作者
Corsten, Maarten F. [1 ]
Shah, Khalid [1 ]
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Boston, MA 02115 USA
关键词
D O I
10.1016/S1470-2045(08)70099-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
As our understanding of stem-cell behaviour rapidly increases, more and more reports suggest that use of stem-cell therapy will extend well beyond regenerative medicine in the near future. Due to their inherent tumoritropic migratory properties, stem cells can serve as vehicles for the delivery of effective, targeted treatment to isolated tumours and to metastatic disease. In vitro, stem cells can readily be engineered by inserting specifically tailored transgenes with antitumour effects to create tumour-seeking therapeutic vehicles. Transgene effects include direct tumour-cell killing, promotion of local immune responses, oncolytic virus production, and prodrug activation schemes. Many of these strategies have been validated in a wide range of studies assessing treatment feasibility or efficacy and establishing methods for real-time monitoring of stem-cell migration and fate in vivo. New insights into avenues for stem-cell sourcing have shortened the probable time to realisation of such treatments for patients. In this Review, we provide an outline of the rationale and status of stem-cell-based treatments fir tumours, and we discuss prospects for clinical implementation and the factors crucial for maintaining momentum towards this goal.
引用
收藏
页码:376 / 384
页数:9
相关论文
共 76 条
[1]
Efficient retrovirus-mediated transfer of the multidrug resistance 1 gene into autologous human long-term repopulating hematopoietic stem cells [J].
Abonour, R ;
Williams, DA ;
Einhorn, L ;
Hall, KM ;
Chen, J ;
Coffman, J ;
Traycoff, CM ;
Bank, A ;
Kato, I ;
Ward, M ;
Williams, SD ;
Hromas, R ;
Robertson, MJ ;
Smith, FO ;
Woo, D ;
Mills, B ;
Srour, EF ;
Cornetta, K .
NATURE MEDICINE, 2000, 6 (06) :652-658
[2]
Neural stem cells display extensive tropism for pathology in adult brain: Evidence from intracranial gliomas [J].
Aboody, KS ;
Brown, A ;
Rainov, NG ;
Bower, KA ;
Liu, SX ;
Yang, W ;
Small, JE ;
Herrlinger, U ;
Ourednik, V ;
Black, PM ;
Breakefield, XO ;
Snyder, EY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) :12846-12851
[3]
Targeting of melanoma brain metastases using engineered neural stem/progenitor cells [J].
Aboody, KS ;
Najbauer, J ;
Schmidt, NO ;
Yang, W ;
Wu, JK ;
Zhuge, Y ;
Przylecki, W ;
Carroll, R ;
Black, PM ;
Perides, G .
NEURO-ONCOLOGY, 2006, 8 (02) :119-126
[4]
Aghi M, 2000, J GENE MED, V2, P148, DOI 10.1002/(SICI)1521-2254(200005/06)2:3<148::AID-JGM105>3.0.CO
[5]
2-Q
[6]
Ligand-targeted therapeutics in anticancer therapy [J].
Allen, TM .
NATURE REVIEWS CANCER, 2002, 2 (10) :750-763
[7]
Can stem cells cross lineage boundaries? [J].
Anderson, DJ ;
Gage, FH ;
Weissman, IL .
NATURE MEDICINE, 2001, 7 (04) :393-395
[8]
Noninvasive MR imaging of magnetically labeled stem cells to directly identify neovasculature in a glioma model [J].
Anderson, SA ;
Glod, J ;
Arbab, AS ;
Noel, M ;
Ashari, P ;
Fine, HA ;
Frank, JA .
BLOOD, 2005, 105 (01) :420-425
[9]
Haematopoietic cell transplantation as immunotherapy [J].
Appelbaum, FR .
NATURE, 2001, 411 (6835) :385-389
[10]
Umbilical-cord blood transplantation for the treatment of cancer [J].
Barker, JN ;
Wagner, JE .
NATURE REVIEWS CANCER, 2003, 3 (07) :526-532