Determining tumor apoptosis and necrosis in patient serum using cytokeratin 18 as a biomarker

被引:118
作者
Linder, S [1 ]
Havelka, AM [1 ]
Ueno, T [1 ]
Shoshan, MC [1 ]
机构
[1] Karolinska Hosp & Inst, Dept Pathol & Oncol, Canc Ctr Karolinska, S-17176 Stockholm, Sweden
关键词
tumor apoptosis; necrosis; cytokeratins;
D O I
10.1016/j.canlet.2004.06.032
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Intracellular macromolecules are released from dying tumor cells and may subsequently be detected in patient blood. In this review, we will discuss the use of cytokeratin-18 as a serum biomarker for monitoring therapy-induced cell death. Cytokeratins are abundant intracellular proteins expressed by most types of carcinoma, but not by treatment-sensitive cells from bone marrow and other tissues. Release of cytokeratins into blood is therefore expected to show some specificity for tumor cell death. Cytokeratin-18 (CK18) is cleaved by caspases specifically during apoptosis, and the molecular form of this protein (caspase-cleaved vs. non-cleaved) released from dying tumor cells is therefore diagnostic as to the type of cell death (apoptosis vs. necrosis). Analyses of different CK18 forms in patient sera have suggested that tumor apoptosis may not necessarily be the dominating death mode in many tumors in vivo. Measurements of increased levels of CK18 in serum during therapy of prostate and breast cancer patients have been encouraging with regard to the possible future use of CK18 as a biomarker for monitoring therapy efficiency. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 65 条
[1]   Detection of circulating tumour DNA in the blood (plasma/serum) of cancer patients [J].
Anker, P ;
Mulcahy, H ;
Chen, XQ ;
Stroun, M .
CANCER AND METASTASIS REVIEWS, 1999, 18 (01) :65-73
[2]   Early changes in apoptosis and proliferation following primary chemotherapy for breast cancer [J].
Archer, CD ;
Parton, M ;
Smith, IE ;
Ellis, PA ;
Salter, J ;
Ashley, S ;
Gui, G ;
Sacks, N ;
Ebbs, SR ;
Allum, W ;
Nasiri, N ;
Dowsett, M .
BRITISH JOURNAL OF CANCER, 2003, 89 (06) :1035-1041
[3]   CA 125 production and release by ovarian cancer cells in vitro [J].
Beck, EP ;
Moldenhauer, A ;
Merkle, E ;
Kiesewetter, F ;
Jäger, W ;
Wildt, L ;
Lang, N .
INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 1998, 13 (04) :200-206
[4]  
Belhocine T, 2002, CLIN CANCER RES, V8, P2766
[5]   Clearance mechanism of prostate specific antigen and its complexes with α2-macroglobulin and α1-antichymotrypsin [J].
Birkenmeier, G ;
Struck, F ;
Gebhardt, R .
JOURNAL OF UROLOGY, 1999, 162 (03) :897-901
[6]   A novel assay for discovery and characterization of pro-apoptotic drugs and for monitoring apoptosis in patient sera [J].
Bivén, K ;
Erdal, H ;
Hägg, M ;
Ueno, T ;
Zhou, R ;
Lynch, M ;
Rowley, B ;
Wood, J ;
Zhang, C ;
Toi, M ;
Shoshan, MC ;
Linder, S .
APOPTOSIS, 2003, 8 (03) :263-268
[7]   Rapid exponential elimination of free prostate-specific antigen contrasts the slow, capacity-limited elimination of PSA complexed to alpha1-antichymotrypsin from serum [J].
Björk, T ;
Ljungberg, B ;
Piironen, T ;
Abrahamsson, PA ;
Pettersson, K ;
Cockett, ATK ;
Lilja, H .
UROLOGY, 1998, 51 (01) :57-62
[8]  
Bjorklund B, 1978, Antibiot Chemother (1971), V22, P16
[9]   Phagocytosis of necrotic cells by macrophages is phosphatidylserine dependent and does not induce inflammatory cytokine production [J].
Brouckaert, G ;
Kalai, M ;
Krysko, DV ;
Saelens, X ;
Vercammen, D ;
Ndlovu, M ;
Haegeman, G ;
D'Herde, K ;
Vandenabeele, P .
MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (03) :1089-1100
[10]   Caspase cleavage of keratin 18 and reorganization of intermediate filaments during epithelial cell apoptosis [J].
Caulin, C ;
Salvesen, GS ;
Oshima, RG .
JOURNAL OF CELL BIOLOGY, 1997, 138 (06) :1379-1394