Author/Editor     Edhemović, I; Snoj, M; Kljun, A; Golouh, R
Title     Immunohistochemical localization of group II phospholipase A2 in the tumours and mucosa of the colon and rectum
Type     članek
Source     Eur J Surg Oncol
Vol. and No.     Letnik 27, št. 6
Publication year     2001
Volume     str. 545-8
Language     eng
Abstract     Background: Group II phospholipase A2 (PLA2) is an enzyme important in malignant transformation and in the invasion process of malignant cells. The aim of the present study was to investigate the expression of group II PLA2 in the cancers of the colorectum, peritumoural mucosa and in the mucosa distant from the tumour. Methods: Resection specimens from 57 patients with colorectal carcinoma (caecum 10, ascending 10, transverse 10, sigmoid colon nine, and rectum 18) were analysed immunohistochemically. Histological slides from paraffin blocks were stained by the human monoclonal group II PLA2 antibody (Upstate Biotechnology, Lake Placid, NY 12946, USA. Antibody Class: IgGIk. Immunogen: HPC perifed human sperm phospholipase A2-14 kDa enzyme) using the standard DAKO peroxidase-labelled streptavidin-biotin method by TechMate 500 stainer. Group II PLA2 expression was evaluated semi-quantitatively according to the extensivity and intensivity of the positive cells. For statistical evaluation the Kruskal-Wallis one way analysis of variance on ranks and the Mann-Whitney rank sum tests were used. Results: The highest expression of group II PLA2 was found in the peritumoural mucosa (median 4.00), much lower in the mucosa distal from the tumour (median 0.70) and almost no activity in the tumour itself (median 0.00), all diferences were statistically significant (all pairwise multiple comparison procedures-Dunns Method: P<0.05). The expression of group II PLA2 was higher in the left colon and rectum than in the right colon (Mann-Whitney rank sum test: P<0.05). Conclusions: Our results suggest that there is variation of the group II PLA2 expression throughout the mucosa and tumours of the colorectum, which might reflect the progression of neoplastic process.
Descriptors     PHOSPHOLIPASES A
COLORECTAL NEOPLASMS
INTESTINAL MUCOSA
IMMUNOHISTOCHEMISTRY