The CXCL12-CXCR4 chemotactic pathway as a target of adjuvant breast cancer therapies

被引:115
作者
Epstein, RJ [1 ]
机构
[1] Univ Hong Kong, Queen Mary Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China
关键词
D O I
10.1038/nrc1473
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Dose-dense adjuvant breast cancer chemotherapy is a new treatment strategy that aims to improve tumour control by using more frequent cytotoxic dosing together with continuous granulocyte colony-stimulating factor (G-CSF) to minimize neutropaenia. In addition to stimulating neutrophil proliferation, G-CSF mobilizes neutrophils from the bone marrow through proteolytic disruption of the chemokine receptor CXCR4 and its chemotactic ligand CXCL12. As breast cancers also express CXCR4 and oestrogen induces CXCL12, the success of dose-dense treatment could partly reflect inhibition of CXCR4-dependent micrometastatic homing and/or paracrine survival, and suggests a benefit of adjuvant oestrogen suppression for patients with oestrogen-receptor-negative, CXCR4-positive disease.
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收藏
页码:901 / 909
页数:10
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共 144 条
[51]  
GYLLENBERG M, 1989, GROWTH DEVELOP AGING, V53, P25
[52]   Stromal cell-derived factor 1, a novel target of estrogen receptor action, mediates the mitogenic effects of estradiol in ovarian and breast cancer cells [J].
Hall, JM ;
Korach, KS .
MOLECULAR ENDOCRINOLOGY, 2003, 17 (05) :792-803
[53]   Chemokine receptor inhibition by AMD3100 is strictly confined to CXCR4 [J].
Hatse, S ;
Princen, K ;
Bridger, G ;
De Clercq, E ;
Schols, D .
FEBS LETTERS, 2002, 527 (1-3) :255-262
[54]   NF-κB promotes breast cancer cell migration and metastasis by inducing the expression of the chemokine receptor CXCR4 [J].
Helbig, G ;
Christopherson, KW ;
Bhat-Nakshatri, P ;
Kumar, S ;
Kishimoto, H ;
Miller, KD ;
Broxmeyer, HE ;
Nakshatri, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (24) :21631-21638
[55]   Comodulation of CXCR4 and CD26 in human lymphocytes [J].
Herrera, C ;
Morimoto, C ;
Blanco, J ;
Mallol, J ;
Arenzana, F ;
Lluis, C ;
Franco, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (22) :19532-19539
[56]   Estrogen receptors and distinct patterns of breast cancer relapse [J].
Hess, KR ;
Pusztai, L ;
Buzdar, AU ;
Hortobagyi, GN .
BREAST CANCER RESEARCH AND TREATMENT, 2003, 78 (01) :105-118
[57]   Hypoxia-induced production of stromal cell-derived factor 1 (CXCL12) and vascular endothelial growth factor by synovial fibroblasts [J].
Hitchon, C ;
Wong, K ;
Ma, GP ;
Reed, J ;
Lyttle, D ;
El-Gabalawy, H .
ARTHRITIS AND RHEUMATISM, 2002, 46 (10) :2587-2597
[58]   Gonadal damage from chemotherapy and radiotherapy [J].
Howell, S ;
Shalet, S .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1998, 27 (04) :927-+
[59]   Proteolytic cleavage of granulocyte colony-stimulating factor and its receptor by neutrophil elastase induces growth inhibition and decreased cell surface expression of the granulocyte colony-stimulating factor receptor [J].
Hunter, MG ;
Druhan, LJ ;
Massullo, PR ;
Avalos, BR .
AMERICAN JOURNAL OF HEMATOLOGY, 2003, 74 (03) :149-155
[60]   Overexpression of CXCR4 on human CD34+ progenitors increases their proliferation, migration, and NOD/SCID repopulation [J].
Kahn, J ;
Byk, T ;
Jansson-Sjostrand, L ;
Petit, I ;
Shivtiel, S ;
Nagler, A ;
Hardan, I ;
Deutsch, V ;
Gazit, Z ;
Gazit, D ;
Karlsson, S ;
Lapidot, T .
BLOOD, 2004, 103 (08) :2942-2949