Cellular and soluble markers of tumor angiogenesis: From patient selection to the identification of the most appropriate postresistance therapy

被引:18
作者
Bertolini, Francesco [1 ,2 ]
Marighetti, Paola [1 ,2 ]
Shaked, Yuval [3 ]
机构
[1] European Inst Oncol, Dept Pathol Lab Med, Lab Hematol Oncol, I-20141 Milan, Italy
[2] European Inst Oncol, Dept Med, Lab Hematol Oncol, I-20141 Milan, Italy
[3] Technion Israel Inst Technol, Rappaport Fac Med, Dept Mol Pharmacol, Haifa, Israel
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2010年 / 1806卷 / 02期
基金
以色列科学基金会;
关键词
Angiogenesis; Oncology endothelial cells; Endothelial progenitors; ENDOTHELIAL GROWTH-FACTOR; METASTATIC COLORECTAL-CANCER; TYROSINE KINASE INHIBITOR; ADVANCED BREAST-CANCER; MARROW-DERIVED CELLS; PHASE-II TRIAL; ANTIANGIOGENIC THERAPY; MAGNETIC-RESONANCE; PROGENITOR CELLS; LUNG-CANCER;
D O I
10.1016/j.bbcan.2010.05.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antiangiogenic drugs are now intensively used in clinical oncology, but some drawbacks still hamper their development. First, it is frequently unclear what patient subpopulation is likely to gain clinical benefit from these expensive therapies: second, there is evidence of (sometimes rapid) development of drug resistance in many patients: third, the results of some preclinical and clinical studies have suggested acceleration of malignant cell aggressiveness when some antiangiogenic therapies are terminated. Here we discuss the role of soluble molecules and cellular markers of neoplastic angiogenesis for patient selection and follow-up during treatment. These markers should help clinicians to decide the right therapy, advise them of the generation of mechanisms of drug resistance during antiangiogenic treatment, and finally suggest the most appropriate next line of therapy according to the new patterns of cancer vascularization induced by antiangiogenic therapies. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:131 / 137
页数:7
相关论文
共 64 条
[1]   AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients [J].
Batchelor, Tracy T. ;
Sorensen, A. Gregory ;
di Tomaso, Emmanuelle ;
Zhang, Wei-Ting ;
Duda, Dan G. ;
Cohen, Kenneth S. ;
Kozak, Kevin R. ;
Cahill, Daniel P. ;
Chen, Poe-Jou ;
Zhu, Mingwang ;
Ancukiewicz, Marek ;
Mrugala, Maciej M. ;
Plotkin, Scott ;
Drappatz, Jan ;
Louis, David N. ;
Ivy, Percy ;
Scadden, David T. ;
Benner, Thomas ;
Loeffler, Jay S. ;
Wen, Patrick Y. ;
Jain, Rakesh K. .
CANCER CELL, 2007, 11 (01) :83-95
[2]   Differential effects of vascular endothelial growth factor receptor-2 inhibitor ZD6474 on circulating endothelial progenitors and mature circulating endothelial cells: Implications for use as a surrogate marker of antiangiogenic activity [J].
Beaudry, P ;
Force, J ;
Naumov, GN ;
Wang, A ;
Baker, CH ;
Ryan, A ;
Soker, S ;
Johnson, BE ;
Folkman, J ;
Heymach, JV .
CLINICAL CANCER RESEARCH, 2005, 11 (09) :3514-3522
[3]  
Bello C, 2006, J CLIN ONCOL, V24, p189S
[4]   Modes of resistance to anti-angiogenic therapy [J].
Bergers, Gabriele ;
Hanahan, Douglas .
NATURE REVIEWS CANCER, 2008, 8 (08) :592-603
[5]   The multifaceted circulating endothelial cell in cancer: towards marker and target identification [J].
Bertolini, Francesco ;
Shaked, Yuval ;
Mancuso, Patrizia ;
Kerbel, Robert S. .
NATURE REVIEWS CANCER, 2006, 6 (11) :833-845
[6]   The multiple personality disorder phenotype(s) of circulating endothelial cells in cancer [J].
Bertolini, Francesco ;
Mancuso, Patrizia ;
Braidotti, Paola ;
Shaked, Yuval ;
Kerbel, Robert S. .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2009, 1796 (01) :27-32
[7]   Circulating endothelial cells - Biomarker of vascular disease [J].
Blann, AD ;
Woywodt, A ;
Bertolini, F ;
Bull, TM ;
Buyon, JP ;
Clancy, RM ;
Haubitz, M ;
Hebbel, RP ;
Lip, GYH ;
Mancuso, P ;
Sampol, J ;
Solovey, A ;
Dignat-George, F .
THROMBOSIS AND HAEMOSTASIS, 2005, 93 (02) :228-235
[8]   Phase II study of sunitinib malate, an oral multitargeted tyrosine kinase inhibitor, in patients with metastatic breast cancer previously treated with an anthracycline and a taxane [J].
Burstein, Harold J. ;
Elias, Anthony D. ;
Rugo, Hope S. ;
Cobleigh, Melody A. ;
Wolff, Antonio C. ;
Eisenberg, Peter D. ;
Lehman, Mary ;
Adams, Bonne J. ;
Bello, Carlo L. ;
DePrimo, Samuel E. ;
Baum, Charles M. ;
Miller, Kathy D. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (11) :1810-1816
[9]   Reversible tumor growth acceleration following bevacizumab interruption in metastatic colorectal cancer patients scheduled for surgery [J].
Cacheux, W. ;
Boisserie, T. ;
Staudacher, L. ;
Vignaux, O. ;
Dousset, B. ;
Soubrane, O. ;
Terris, B. ;
Mateus, C. ;
Chaussade, S. ;
Goldwasser, F. .
ANNALS OF ONCOLOGY, 2008, 19 (09) :1659-1661
[10]   Predictive Potential of Angiogenic Growth Factors and Circulating Endothelial Cells in Breast Cancer Patients Receiving Metronomic Chemotherapy Plus Bevacizumab [J].
Calleri, Angelica ;
Bono, Anna ;
Bagnardi, Vincenzo ;
Quarna, Jessica ;
Mancuso, Patrizia ;
Rabascio, Cristina ;
Dellapasqua, Silvia ;
Campagnoli, Elisabetta ;
Shaked, Yuval ;
Goldhirsch, Aron ;
Colleoni, Marco ;
Bertolini, Francesco .
CLINICAL CANCER RESEARCH, 2009, 15 (24) :7652-7657