Cancer Stem Cells and the Tumor Microenvironment: Soloists or Choral Singers

被引:35
作者
Albini, A. [1 ,2 ]
Cesana, E.
Noonan, D. M. [3 ]
机构
[1] IRCCS MultiMed, Multimed Castellanza VA, I-20138 Milan, Italy
[2] MultiMedica, Casa Cura, S Maria, Castellanza, Italy
[3] Univ Insubria, Dept Expt Med, Varese, Italy
关键词
Cancer stem cell; stemness control; microenvironment; surface markers; niche; matrigel; miRNA; models; ACUTE LYMPHOBLASTIC-LEUKEMIA; CHRONIC MYELOID-LEUKEMIA; INITIATING CELLS; BREAST-CANCER; MESENCHYMAL TRANSITION; ALOX5; GENE; GROWTH; IDENTIFICATION; PROLIFERATION; ANGIOGENESIS;
D O I
10.2174/138920111794295756
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The idea of cancer stem cell (CSC) has recently moved to the forefront of cancer research. There is still a lack of a widespread consensus on the of these cells, description and definition. The increasing literature on CSCs has compelled researchers worldwide to rewrite the natural history of cancer including those cells as principal players as well as to revise their views on tumor formation and progression. CSCs are tumor cell components that can initiate a new tumor after an apparent therapeutic eradication. A functional definition of cancer stem cell or cancer initiating cell is that of a cell which, when transplanted in a mouse model, can give rise to a tumor recapitulating the original one or even a phenotypically diverse tumor related to the tumor of origin. Since the characteristic asymmetric division of stem cells is somewhat anomalous in cancer, it might be advisable to refer to them as "stemloids". Stemness in cancer is not as much as an identity but rather a status. There is increasing evidence of the importance of the tumor and the host microenvironment in conditioning the stem cell status itself. The cancer stem cell microenvironment may be the key in the development of therapeutic strategies. We must think in terms of targeting "standard" tumor cells, cancer stem cells, and also their niche and tumor microenvironment. Here we discuss some features of cancer stem cells, and the role of the microenvironment, envisaging a choral view of cancer stem cell development and-or latency, towards development of specific therapeutic approaches. Here we propose models of replication and quiescence and the modulation by cells, genes and miRNAs. We also summarize in a table surface markers useful for the identification and isolation of CSCs.
引用
收藏
页码:171 / 181
页数:11
相关论文
共 63 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]
MATRIGEL PROMOTES RETINOBLASTOMA CELL-GROWTH INVITRO AND INVIVO [J].
ALBINI, A ;
MELCHIORI, A ;
GAROFALO, A ;
NOONAN, DM ;
BASOLO, F ;
TARABOLETTI, G ;
CHADER, GJ ;
GIAVAZZI, R .
INTERNATIONAL JOURNAL OF CANCER, 1992, 52 (02) :234-240
[3]
[Anonymous], NAT REP STEM CELLS
[4]
[Anonymous], CBTRUS STAT REP PRIM
[5]
Stem cell-like glioma cells promote tumor angiogenesis through vascular endothelial growth factor [J].
Bao, Shideng ;
Wu, Qiulian ;
Sathornsumetee, Sith ;
Hao, Yueling ;
Li, Zhizhong ;
Hjelmeland, Anita B. ;
Shi, Oing ;
McLendon, Roger E. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
CANCER RESEARCH, 2006, 66 (16) :7843-7848
[6]
Cancer stem cell and cancer stemloids [J].
Blagosklonny, Mikhail V. .
CANCER BIOLOGY & THERAPY, 2007, 6 (11) :1684-1690
[7]
Opinion -: Invasive growth:: a MET-driven genetic programme for cancer and stem cells [J].
Boccaccio, Carla ;
Comoglio, Paolo M. .
NATURE REVIEWS CANCER, 2006, 6 (08) :637-645
[8]
Reprogramming cell fates in the mammary microenvironment [J].
Boulanger, Corinne A. ;
Smith, Gilbert H. .
CELL CYCLE, 2009, 8 (08) :1127-1132
[9]
The hunt for cancer-initiating cells: a history stemming from leukemia [J].
Buzzeo, M. P. ;
Scott, E. W. ;
Cogle, C. R. .
LEUKEMIA, 2007, 21 (08) :1619-1627
[10]
A perivascular niche for brain tumor stem cells [J].
Calabrese, Christopher ;
Poppleton, Helen ;
Kocak, Mehmet ;
Hogg, Twala L. ;
Fuller, Christine ;
Hamner, Blair ;
Oh, Eun Young ;
Gaber, M. Waleed ;
Finklestein, David ;
Allen, Meredith ;
Frank, Adrian ;
Bayazitov, Ildar T. ;
Zakharenko, Stanislav S. ;
Gajjar, Amar ;
Davidoff, Andrew ;
Gilbertson, Richard J. .
CANCER CELL, 2007, 11 (01) :69-82