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. 2006 Aug;87(4):297-306.
doi: 10.1111/j.1365-2613.2006.00482.x.

Alterations of p53, BCL-2, and hMSH2 protein expression in the normal brain tissues, gliosis, and gliomas

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Alterations of p53, BCL-2, and hMSH2 protein expression in the normal brain tissues, gliosis, and gliomas

Mahmoud R Hussein et al. Int J Exp Pathol. 2006 Aug.

Abstract

Tumorigenesis involves alterations in the tumor suppressor genes (p53), protooncogenes (BCL-2), and housekeeping genes (human MutS homologue-2 (hMSH2). We hypothesized that development of gliomas is associated with alterations of p53, BCL-2, and hMSH2 protein expression. To test our hypothesis and to examine these issues, we immunostained 60 specimens entailing normal brain tissues, gliosis, and gliomas (Grade I, II, III, IV) for p53, BCL-2, and hMSH2 protein expression. As compared with the normal brain and gliosis, examination of the average weighted scores in gliomas (Grade I, II, III, IV, respectively) showed significant up-regulation of: (i) p53 protein (0.0 +/- 0.0; 0.0 +/- 0.0; 0.9 +/- 0.5; 1.6 +/- 0.8; 1.7 +/- 0.5; and 4.1 +/- 0.8, P < 0.0001) (ii) hMSH2 (1.3 +/- 0.3; 1.5 +/- 0.7; 1.9 +/- 1.1; 2.2 +/- 0.5; 4.1 +/- 1.5; and 4.7 +/- 1.1, P < 0.0006), and (iii) BCL-2 (0.8 +/- 0.5; 1.9 +/- 0.5; 1.9 +/- 0.6; 2.0 +/- 0.6; 4.4 +/- 1.2; and 4.6 +/- 0.8, P < 0.001). The expression values (p53, BCL-2, and hMSH2) were statistically significantly higher (P < 0.05) in astrocytomas (Grade III) than in other gliomas. There was an insignificant negative correlation between p53 and BCL-2 (r = -0.07, P > 0.05) and between p53 and hMSH2 (r = -0.08, P > 0.05) protein expression. Alterations of the p53, BCL-2, and hMSH2 proteins occur during the development of these tumors.

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Figures

Figure 1
Figure 1
Immunoreactivity scores of p53, BCL-2, and hMSH2 proteins in (a) normal brain, gliosis, ependymoma, and oligodendroglioma; (b) in normal brain, and astrocytomas (Grades I, II, III, IV); (c) normal brain, gliosis, and gliomas, and (d) histological characteristics of gliomas (Cellularity, pleomorphism, mitosis, microvascular proliferation). MMR, mismatch repair system.
Figure 2
Figure 2
Positive controls p53 protein nuclear expression pattern in the squamous cell carcinoma. BCL-2 protein cytoplasmic expression pattern in the lymph node (reactive hyperplasia) in the mantle zone with negative reactivity in the germ centres. hMSH2 protein nuclear expression pattern in the skin (normal epidermis).
Figure 3
Figure 3
Immunohistochemical staining of p53 protein in the normal brain, gliosis, and different grades of gliomas (nuclear expression, ×400).
Figure 4
Figure 4
Immunohistochemical staining of BCL-2 protein in the normal brain, gliosis, and different grades of gliomas (cytoplasmic expression, ×400).
Figure 5
Figure 5
Immunohistochemical staining of hMSH2 protein in the normal brain, gliosis, and different grades of gliomas (nuclear expression, ×400).

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