Expression pattern of chemokine receptor 6 (CCR6) and CCR7 in squamous cell carcinoma of the head and neck identifies a novel metastatic phenotype

被引:134
作者
Wang, J
Xi, LQ
Hunt, JL
Gooding, W
Whiteside, TL
Chen, Z
Godfrey, TE
Ferris, RL
机构
[1] Univ Pittsburgh, Inst Canc, Hillman Canc Ctr, Dept Otolaryngol, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Inst Canc, Hillman Canc Ctr, Dept Immunol, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Inst Canc, Dept Surg, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Inst Canc, Dept Biostat, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Sch Med, Dept Otolaryngol & Immunol, Pittsburgh, PA 15260 USA
[6] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15260 USA
关键词
D O I
10.1158/0008-5472.CAN-03-2968
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Squamous cell carcinoma of the head and neck (SCCHN) metastasizes predictably to cervical lymph nodes, with low rates of distant metastases. Tumor cells can express various receptors that facilitate such metastatic spread to lymph nodes and other nonlymphoid organs. Chemokine receptors (CCR), normally expressed on lymphocytes, control immune and inflammatory cell migration, providing a link between innate and adaptive immunity. Chemokine receptor expression was evaluated in SCCHN, using paired primary and metastatic tumors cell lines, and paired primary and metastatic biopsies from the same patients. Quantitative reverse transcription-PCR showed a consistent pattern of CCR6 down-regulation and up-regulation of CCR7 in metastatic cells and tissues. Chemotaxis assays, ligand-induced receptor down-regulation, and specific antibody blocking experiments supported the quantitative reverse transcription-PCR results, indicating that these surface receptors were functional on metastatic tumor cells. Cells derived from a highly metastatic mouse model of SCCHN were used to confirm CCR7 up-regulation in tumor cells with higher metastatic potential. CCR6 down-regulation is consistent with its decreased expression in cells emigrating from peripheral mucosal sites, whereas CCR7, important for homing of immune cells to secondary lymphoid organs, was significantly up-regulated. Thus, CCR6, CCR7, and their ligands, normally important in controlling immune cell trafficking in response to inflammatory stimuli, may have an important role in determining the metastasis of SCCHN cells in vivo.
引用
收藏
页码:1861 / 1866
页数:6
相关论文
共 34 条
[1]   Lymphocyte trafficking and regional immunity [J].
Butcher, EC ;
Williams, M ;
Youngman, K ;
Rott, L ;
Briskin, M .
ADVANCES IN IMMUNOLOGY, VOL. 72, 1999, 72 :209-253
[2]   Chemokines in tissue-specific and microenvironment-specific lymphocyte homing [J].
Campbell, JJ ;
Butcher, EC .
CURRENT OPINION IN IMMUNOLOGY, 2000, 12 (03) :336-341
[3]   Chemokines and the arrest of lymphocytes rolling under flow conditions [J].
Campbell, JJ ;
Hedrick, J ;
Zlotnik, A ;
Siani, MA ;
Thompson, DA ;
Butcher, EC .
SCIENCE, 1998, 279 (5349) :381-384
[4]   Dissemination and growth of cancer cells in metastatic sites [J].
Chambers, AF ;
Groom, AC ;
MacDonald, IC .
NATURE REVIEWS CANCER, 2002, 2 (08) :563-572
[5]   Comparison of gene expression between metastatic derivatives and their poorly metastatic parental cells implicates crucial tumor-environment interaction in metastasis of head and neck squamous cell carcinoma [J].
Chen, Z ;
Zhang, K ;
Zhang, X ;
Yuan, XH ;
Yuan, ZY ;
Jin, L ;
Xiong, M .
CLINICAL & EXPERIMENTAL METASTASIS, 2003, 20 (04) :335-342
[6]   Dendritic cell migration in different micropore filter assays [J].
Dunzendorfer, S ;
Kaser, A ;
Meierhofer, C ;
Tilg, H ;
Wiedermann, CJ .
IMMUNOLOGY LETTERS, 2000, 71 (01) :5-11
[7]   BIOLOGICAL DIVERSITY IN METASTATIC NEOPLASMS - ORIGINS AND IMPLICATIONS [J].
FIDLER, IJ ;
HART, IR .
SCIENCE, 1982, 217 (4564) :998-1003
[8]   CCR7 coordinates the primary immune response by establishing functional microenvironments in secondary lymphoid organs [J].
Förster, R ;
Schubel, A ;
Breitfeld, D ;
Kremmer, E ;
Renner-Müller, I ;
Wolf, E ;
Lipp, M .
CELL, 1999, 99 (01) :23-33
[9]   Neck disease and distant metastases [J].
Genden, EM ;
Ferlito, A ;
Bradley, PJ ;
Rinaldo, A ;
Scully, C .
ORAL ONCOLOGY, 2003, 39 (03) :207-212
[10]   Quantitative mRNA expression analysis from formalin-fixed, paraffin-embedded tissues using 5′ nuclease quantitative reverse transcription-polymerase chain reaction [J].
Godfrey, TE ;
Kim, SH ;
Chavira, M ;
Ruff, DW ;
Warren, RS ;
Gray, JW ;
Jensen, RH .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2000, 2 (02) :84-91