Chromatin-bound PCNA as S-phase marker in mononuclear blood cells of patients with acute lymphoblastic leukaemia or multiple myeloma

被引:9
|
作者
Zoelzer, F. [1 ,2 ]
Basu, O. [3 ]
Devi, P. U. [4 ]
Mohanty, S. P. [5 ]
Streffer, C. [2 ]
机构
[1] Univ S Bohemia, Dept Radiol & Toxicol, Fac Hlth & Social Studies, Ceske Budejovice 37001, Czech Republic
[2] Univ Duisburg Essen, Dept Med Radiobiol, Fac Med, Essen, Germany
[3] Univ Duisburg Essen, Dept Paediat Oncol, Fac Med, Essen, Germany
[4] Kasturba Med Coll & Hosp, Dept Radiobiol, Manipal, Karnataka, India
[5] Kasturba Med Coll & Hosp, Dept Orthopaed, Manipal, Karnataka, India
关键词
FLOW-CYTOMETRIC ANALYSIS; DNA POLYMERASE-DELTA; NUCLEAR ANTIGEN; MONOCLONAL-ANTIBODIES; AUXILIARY PROTEIN; PROGNOSTIC VALUE; CYCLIN; PROLIFERATION; REPLICATION; FRACTION;
D O I
10.1111/j.1365-2184.2010.00707.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objectives: Proliferating cell nuclear antigen (PCNA) has often been used as a marker to aid assessment of tumour growth fraction. This paper addresses the question of whether it can be used as an S-phase marker, when the non-chromatin-bound form of the protein is removed by pepsin treatment. Materials and methods: Cytofluorometric measurements were carried out after immunofluorescence staining of PCNA and counterstaining of DNA. S-phase fraction was determined with the help of windows on PCNA versus DNA scattergrams, or mathematically from DNA histograms. Results: S-phase fractions obtained using the two methods correlated well, but did not always agree, exact discrepancies depending on the mathematical model used for histogram analysis. Conclusions: Determination of S-phase fractions with the help of PCNA immunofluorescence staining is possible, and probably more reliable than calculation of S-fractions from DNA histograms. It thus offers an alternative to assays involving BrdU labelling in vivo.
引用
收藏
页码:579 / 583
页数:5
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