Serum level of macrophage colony-stimulating factor is increased in prostate cancer patients with bone metastasis

被引:34
作者
Ide, Hisamitsu [1 ]
Hatake, Kiyohiko [3 ]
Terado, Yuichi [2 ]
Tsukino, Hiroyuki [4 ]
Okegawa, Takatsugu [5 ]
Nutahara, Kikuo [5 ]
Higashihara, Eiji [5 ]
Horie, Shigeo [1 ]
机构
[1] Teikyo Univ, Sch Med, Dept Urol, Itabashi Ku, Tokyo 1738605, Japan
[2] Kyorin Univ, Sch Med, Dept Pathol, Mitaka, Tokyo 181, Japan
[3] Japanese Fdn Canc Res, Dept Med Oncol, Canc Inst Hosp, Koutou Ku, Mitaka, Tokyo, Japan
[4] Miyazaki Univ, Dept Urol, Sch Med, Miyazaki, Japan
[5] Kyorin Univ, Sch Med, Dept Urol, Mitaka, Tokyo 181, Japan
关键词
bone metastasis; macrophage colony-stimulating factor; prostate cancer;
D O I
10.1111/j.1749-0774.2007.00042.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Recent evaluation of human prostate tissues has shown predominantly high expression of the macrophage colony-stimulating factor receptor in prostatic intra-epithelial neoplasia or prostate cancer. However, the expression of its ligand, the macrophage colony-stimulating factor (M-CSF), and the biological role of this signaling in prostate cancer has not been analyzed. In this research we determined the relationship of serum M-CSF level to clinical parameters of prostate cancer progression. We measured the serum level of M-CSF in 170 patients with histologically confirmed prostatic adenocarcinoma and in 54 patients in whom prostate cancer was not detected. We also investigated the M-CSF expression in prostate cancer tissues by immunohistochemistry. The serum levels of M-CSF in bone metastatic prostate cancer patients was significantly higher than those in non-metastatic patients, while M-CSF did not differ with regards to histological grade, Gleason score or local tumor progression. M-CSF expression was detected in prostate cancer cells themselves by immunohistochemistry. These results suggest that M-CSF may have a functional role in prostate cancer progression.
引用
收藏
页码:1 / 6
页数:6
相关论文
共 32 条
[1]
Colony-stimulating factor-1 blockade by antisense oligonucleotides and small interfering RNAs suppresses growth of human mammary tumor xenografts in mice [J].
Aharinejad, S ;
Paulus, P ;
Sioud, M ;
Hofmann, M ;
Zins, K ;
Schäfer, R ;
Stanley, ER ;
Abraham, D .
CANCER RESEARCH, 2004, 64 (15) :5378-5384
[2]
Cecchini MG, 1997, MOL REPROD DEV, V46, P75
[3]
Djakiew D, 2000, PROSTATE, V42, P150, DOI 10.1002/(SICI)1097-0045(20000201)42:2<150::AID-PROS10>3.0.CO
[4]
2-H
[5]
Therapeutic potential of curcumin in prostate cancer - IV: Interference with the osteomimetic properties of hormone refractory C4-2B prostate cancer cells [J].
Dorai, T ;
Dutcher, JP ;
Dempster, DW ;
Wiernik, PH .
PROSTATE, 2004, 60 (01) :1-17
[6]
MACROPHAGE-COLONY-STIMULATING FACTOR-1, A CLINICALLY USEFUL TUMOR-MARKER IN ENDOMETRIAL ADENOCARCINOMA - COMPARISON WITH CA-125 AND THE AMINOTERMINAL PROPEPTIDE OF TYPE-III PROCOLLAGEN [J].
HAKALA, A ;
KACINSKI, BM ;
STANLEY, ER ;
KOHORN, EI ;
PUISTOLA, U ;
RISTELI, J ;
RISTELI, L ;
TOMAS, C ;
KAUPPILA, A .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1995, 173 (01) :112-119
[7]
Expression of colony-stimulating factor 1 receptor during prostate development and prostate cancer progression [J].
Ide, H ;
Seligson, DB ;
Memarzadeh, S ;
Xin, L ;
Horvath, S ;
Dubey, P ;
Flick, MB ;
Kacinski, BM ;
Palotie, A ;
Witte, ON .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (22) :14404-14409
[8]
High serum levels of M-CSF and G-CSF in Kawasaki disease [J].
Igarashi, H ;
Hatake, K ;
Tomizuka, H ;
Yamada, M ;
Gunji, Y ;
Momoi, MY .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 105 (03) :613-615
[9]
Kacinski BM, 1997, MOL REPROD DEV, V46, P71, DOI 10.1002/(SICI)1098-2795(199701)46:1<71::AID-MRD11>3.0.CO
[10]
2-6