Angiogenesis in gliomas

被引:27
作者
Lebelt, Agnieszka [1 ]
Dzieciol, Janusz [1 ]
Guzinska-Ustymowicz, Katarzyna [2 ]
Lemancewicz, Dorota [1 ]
Zimnoch, Lech [3 ]
Czykier, Elzbieta [4 ]
机构
[1] Med Univ Bialystok, Dept Human Anat, PL-15230 Bialystok, Poland
[2] Med Univ Bialystok, Dept Gen Pathomorphol, PL-15230 Bialystok, Poland
[3] Med Univ Bialystok, Dept Med Pathomorphol, PL-15230 Bialystok, Poland
[4] Med Univ Bialystok, Dept Histol, PL-15230 Bialystok, Poland
关键词
angiogenesis; glioma; Ki-67; PCNA; microvascular proliferation; microvessel density;
D O I
10.2478/v10042-008-0009-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Brain gliomas are characterized by invasive growth and neovascularisation potential. Angiogenesis plays a major role in the progression of gliomas and its determination has a great prognostic value. The aim of the study was to assess the vascularisation of chosen brain gliomas and to estimate how it is correlated with tumour histological type, malignancy grade, location and size, and with age and sex of patients. Tumour vascularisation analysis was based on the determination of microvascular proliferation (MVP) and microvessel density (MVD). Microvascular proliferation was measured with immunohistochemical methods using mouse monoclonal antibodies to detect cell proliferation antigens. The following antibodies were used Ki-67 and PCNA (DAKO). Identification of vessels was performed by CD31 antibody and anti-human von Willebrand factor (DAKO). The highest microvascular proliferation and microvascular density were observed in multiform glioblastomas and the lowest in oligodendrogliomas. Significant correlation was observed between the vascularisation and malignancy grade.
引用
收藏
页码:69 / 72
页数:4
相关论文
共 21 条
  • [1] Assimakopoulou M, 1997, ANTICANCER RES, V17, P4747
  • [2] Vascular patterns in glioblastoma influence clinical outcome and associate with variable expression of angiogenic proteins:: Evidence for distinct angiogenic subtypes
    Birner, P
    Piribauer, M
    Fischer, I
    Gatterbauer, B
    Marosi, C
    Ambros, PF
    Ambros, IM
    Bredel, M
    Oberhuber, G
    Rössler, K
    Budka, H
    Harris, AL
    Hainfellner, JA
    [J]. BRAIN PATHOLOGY, 2003, 13 (02) : 133 - 143
  • [3] Carroll RS, 1999, CANCER-AM CANCER SOC, V86, P1335, DOI 10.1002/(SICI)1097-0142(19991001)86:7<1335::AID-CNCR32>3.0.CO
  • [4] 2-Z
  • [5] FOLKMAN J, 1971, NEW ENGL J MED, V285, P1182
  • [6] WHAT IS THE EVIDENCE THAT TUMORS ARE ANGIOGENESIS DEPENDENT
    FOLKMAN, J
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1990, 82 (01): : 4 - 6
  • [7] High microvessel density in primitive neuroectodermal brain tumors of childhood
    Grotzer, MA
    Wiewrodt, R
    Janss, AJ
    Zhao, HQ
    Cnaan, A
    Sutton, LN
    Rorke, LB
    Phillips, PC
    [J]. NEUROPEDIATRICS, 2001, 32 (02) : 75 - 79
  • [8] Gupta K, 2004, ANAL QUANT CYTOL, V26, P223
  • [9] Izycka-Swleszewska E, 2003, FOLIA NEUROPATHOL, V41, P15
  • [10] Proliferative activity of microvascular cells in glioblastomas does not correlate with time to recurrence
    Kern, MA
    Feisel, KD
    Friese, M
    Ernestus, RI
    Schröder, R
    [J]. JOURNAL OF NEURO-ONCOLOGY, 2003, 63 (01) : 9 - 13