Role of CXCR4 and SDF-1 in mammary tumor metastasis in the cat

被引:14
|
作者
Oonuma, T
Morimatsu, M [1 ]
Nakagawa, T
Uyama, R
Sasaki, N
Nakaichi, M
Tamamura, H
Fuji, N
Hashimoto, S
Yamamura, H
Syuto, B
机构
[1] Iwate Univ, Fac Agr, Vet Physiol Lab, Morioka, Iwate 0208550, Japan
[2] Univ Tokyo, Grad Sch Agr & Life Sci, Div Vet Med Sci, Lab Vet Surg,Bunkyo Ku, Tokyo 1138657, Japan
[3] Yamaguchi Univ, Fac Agr, Dept Vet Surg, Yamaguchi 7538515, Japan
[4] Kitagawa Anim Hosp, Itabashi Ku, Tokyo 1740072, Japan
[5] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan
来源
JOURNAL OF VETERINARY MEDICAL SCIENCE | 2003年 / 65卷 / 10期
关键词
CXCR4; feline; mammary tumor; metastasis; SDF-1;
D O I
10.1292/jvms.65.1069
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
It has recently been suggested that the chemokine receptor CXCR4 and its ligand SDF-1 (CXCL12) promote metastasis of various cancers in humans. Since feline mammary tumors also metastasize to distant organs frequently, we used real-time quantitative PCR to examine the expression of feline CXCR4 (fCXCR4) in ten feline mammary tumor cell lines and seven feline mammary tumor tissues, and also the expression of feline SDF-1 (fSDF-1) in various organs. Cell lines derived from metastatic regions expressed more fCXCR4 than those derived from primary tumors. Mammary tumor tissues overexpressed more fCXCR4 than normal mammary tissues. Organs with high levels of fSDF-1 expression represent common sites of metastasis. Migration assays using the feline mammary tumor cell line NAC were also performed to test the activity of TN14003 and TC14012, antagonists of human CXCR4, to antagonize fCXCR4 expressed on NAC cells. TN14003 and TC14012 inhibited migration of NAC cells. We conclude that fCXCR4 may be a therapeutic target for feline mammary tumors.
引用
收藏
页码:1069 / 1073
页数:5
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