Ki67, PCNA, and MCM proteins: Markers of proliferation in the diagnosis of breast cancer

被引:617
作者
Jurikova, Miroslava [1 ]
Danihel, Ludovit [2 ]
Polak, Stefan [1 ]
Varga, Ivan [1 ]
机构
[1] Comenius Univ, Fac Med, Inst Histol & Embryol, Spitalska 24, Bratislava 81372, Slovakia
[2] Comenius Univ, Fac Med, Inst Pathol Anat, Spitalska 24, Bratislava 81372, Slovakia
关键词
Proliferative markers; Ki67; PCNA; MCM; Breast cancer; Diagnosis; Prognosis; CELL NUCLEAR ANTIGEN; MINICHROMOSOME MAINTENANCE PROTEINS; CHROMOSOMAL DNA-REPLICATION; ORIGIN RECOGNITION COMPLEX; LYMPH-NODE METASTASES; PROGNOSTIC MARKER; KI-67; EXPRESSION; MONOCLONAL-ANTIBODIES; MITOTIC CHROMOSOMES; INTERNATIONAL KI67;
D O I
10.1016/j.acthis.2016.05.002
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The proliferative activity of tumour cells represents an important prognostic marker in the diagnosis of cancer. One of the methods for assessing the proliferative activity of cells is the immunohistochemical detection of cell cycle-specific antigens. For example, Ki67, proliferating cell nuclear antigen (PCNA), and minichromosome maintenance (MCM) proteins are standard markers of proliferation that are commonly used to assess the growth fraction of a cell population. The function of Ki67, the widely used marker of proliferation, still remains unclear. In contrast, PCNA and MCM proteins have been identified as important participants of DNA replication. All three proteins only manifest their expression during the cell division of normal and neoplastic cells. Since the expression of these proliferative markers was confirmed in several malignant tumours, their prognostic and predictive values have been evaluated to determine their significance in the diagnosis of cancer. This review offers insight into the discovery of the abovementioned proteins, as well as their current molecular and biological importance. In addition, the functions and properties of all three proteins and their use as markers of proliferation in the diagnosis of breast cancer are described. This work also reveals new findings about the role of Ki67 during the mitotic phase of the cell cycle. Finally, information is provided about the advantages and disadvantages of using all three antigens in the diagnosis of cancer. (C) 2016 Elsevier GmbH. All rights reserved.
引用
收藏
页码:544 / 552
页数:9
相关论文
共 131 条
[61]
Chromatin binding of the fission yeast replication factor mcm4 occurs during anaphase and requires ORC and cdc18 [J].
Kearsey, SE ;
Montgomery, S ;
Labib, K ;
Lindner, K .
EMBO JOURNAL, 2000, 19 (07) :1681-1690
[62]
MCM proteins: evolution, properties, and role in DNA replication [J].
Kearsey, SE ;
Labib, K .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1998, 1398 (02) :113-136
[63]
Kill IR, 1996, J CELL SCI, V109, P1253
[64]
Mouse MCM proteins: Complex formation and transportation to the nucleus [J].
Kimura, H ;
Ohtomo, T ;
Yamaguchi, M ;
Ishii, A ;
Sugimoto, K .
GENES TO CELLS, 1996, 1 (11) :977-993
[65]
Standardized Ki67 Diagnostics Using Automated Scoring-Clinical Validation in the GeparTrio Breast Cancer Study [J].
Klauschen, Frederick ;
Wienert, Stephan ;
Schmitt, Wolfgang D. ;
Loibl, Sibylle ;
Gerber, Bernd ;
Blohmer, Jens-Uwe ;
Huober, Jens ;
Ruediger, Thomas ;
Erbstoesser, Erhard ;
Mehta, Keyur ;
Lederer, Bianca ;
Dietel, Manfred ;
Denkert, Carsten ;
von Minckwitz, Gunter .
CLINICAL CANCER RESEARCH, 2015, 21 (16) :3651-3657
[66]
A direct interaction between proliferating cell nuclear antigen (PCNA) and Cdk2 targets PCNA-interacting proteins for phosphorylation [J].
Koundrioukoff, S ;
Jónsson, ZO ;
Hasan, S ;
de Jong, RN ;
van der Vliet, PC ;
Hottiger, MO ;
Hübscher, U .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (30) :22882-22887
[67]
Krude T, 1996, J CELL SCI, V109, P309
[68]
Kwok HF, 2015, AM J CANCER RES, V5, P52
[69]
Uninterrupted MCM2-7 function required for DNA replication fork progression [J].
Labib, K ;
Tercero, JA ;
Diffley, JFX .
SCIENCE, 2000, 288 (5471) :1643-1647
[70]
Transfer of the MSH2•MSH6 complex from proliferating cell nuclear antigen to mispaired bases in DNA [J].
Lau, PJ ;
Kolodner, RD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (01) :14-17