Kallikreins as markers of disseminated tumour cells in ovarian cancer - A pilot study

被引:20
作者
Oikonomopoulou, K
Scorilas, A
Michael, IP
Grass, L
Soosaipillai, A
Rosen, B
Murphy, J
Diamandis, EP
机构
[1] Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[3] Princess Margaret Hosp, Gynecol Oncol Clin, Toronto, ON M4X 1K9, Canada
[4] Univ Athens, Fac Biol, Dept Biochem & Mol Biol, Athens, Greece
关键词
human kallikreins; serine proteases; metastasis; blood dissemination; ascites fluid;
D O I
10.1159/000092325
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Kallikreins are a family of secreted serine proteases, encoded by 15 genes which all localize in tandem on chromosome 19q13.4. Several members of this family have been previously associated with ovarian cancer. Kallikreins 6 (KLK6) and 10 (KLK10) are elevated in tumour cells, serum and ascites fluid of ovarian cancer patients and correlate with disease prognosis. Other kallikreins that have been related to ovarian cancer include KLK4, 5, 7, 8, 9, 11, 13, 14 and 15. We hypothesized that KLK6 and KLK10 can be utilized to monitor dissemination of ovarian cancer cells in blood and ascites fluid of ovarian cancer patients. Methods: RNA was isolated by immunomagnetic separation of cancer cells and was amplified by RT-PCR. Results: Screening for disseminated cancer cells in blood from 24 ovarian cancer patients, with RT-PCR for KLK6 mRNA, resulted in 75% positivity; however, this was not different from the positivity of normal controls. By utilizing KLK10 as a marker, the positivity of patients was 40% versus 20% of controls. Screening of ascites fluid of ovarian cancer patients revealed 90% positivity for KLK6 and KLK10 mRNA compared with 33% for other cancer types. Significant correlations were identified among mRNA of KLK4,5, 6,7, 8, 9,10,11, 13,14 and 15 in cancer cells isolated from ascites fluid. Conclusion: Kallikrein expression by ovarian cancer cells is not specific enough for detecting disseminated disease. Kallikrein expression may have some value for differentiating ovarian cancer from other types of cancer or from non-malignant diseases that lead to ascites accumulation. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:104 / 114
页数:11
相关论文
共 54 条
[1]  
Agarwal Roshan, 2004, Proceedings of the American Association for Cancer Research Annual Meeting, V45, P1028
[2]   Endothelial cell serine proteases expressed during vascular morphogenesis and angiogenesis [J].
Aimes, RT ;
Zijlstra, A ;
Hooper, JD ;
Ogbourne, SM ;
Sit, ML ;
Fuchs, S ;
Gotley, DC ;
Quigley, JP ;
Antalis, TM .
THROMBOSIS AND HAEMOSTASIS, 2003, 89 (03) :561-572
[3]  
*AM CANC SOC, 2004, FACTS FIG 2004
[4]  
[Anonymous], 2003, J. Clin. Oncol, DOI DOI 10.1200/JCO.2003.01.068
[5]   Targeting kallikrein 6-proteolysis attenuates CNS inflammatory disease [J].
Blaber, SI ;
Ciric, B ;
Christophi, GP ;
Bernett, MJ ;
Blaber, M ;
Rodriguez, M ;
Scarisbrick, IA .
FASEB JOURNAL, 2004, 18 (03) :920-+
[6]   The emerging roles of human tissue kallikreins in cancer [J].
Borgoño, CA ;
Diamandis, EP .
NATURE REVIEWS CANCER, 2004, 4 (11) :876-890
[7]  
Borgoño CA, 2004, MOL CANCER RES, V2, P257
[8]  
Bracete A.M., 1999, FOCUS, V21, P38
[9]   Effect of collection, transport, processing and storage of blood specimens on the activity of lysosomal enzymes in plasma and leukocytes [J].
Burin, M ;
Dutra, C ;
Brum, J ;
Mauricio, T ;
Amorim, M ;
Giugliani, R .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2000, 33 (09) :1003-1013
[10]   ILLEGITIMATE (OR ECTOPIC) TRANSCRIPTION PROCEEDS THROUGH THE USUAL PROMOTERS [J].
CHELLY, J ;
HUGNOT, JP ;
CONCORDET, JP ;
KAPLAN, JC ;
KAHN, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 178 (02) :553-557