Gliomas are among the most aggressive and treatment-refractory of all human tumors. The aim of the present study is to evaluate the role of the expression of cell cycle molecules as prognostic indicators in gliomas. We immunohistochemically analyzed the expression of p21, p27, p14, p16, p53 and proliferation marker Ki67, in 67 low and high grade astrocytic tumors. High grade tumors exhibited higher labeling indices for Ki67 (P = 0.004), p53 (P = 0.039) and slightly higher index for p21 (P = 0.07) compared to low grade tumors. p14 and p16 were more frequently present in low grade tumors (P = 0.001 and P = 0.052, respectively). Worse survival was correlated with high grade tumors (P < 0.0001) and higher Ki67 index (P < 0.0001). Cox regression analysis revealed that only age, grade and marginally Ki67 index were independent prognostic factors. Cell cycle alterations are involved in the malignant progression of astrocytomas, but only age, tumor grade and proliferating index can predict the outcome of the patients with glioma.

Twelve C-terminal heptapeptide analogues of substance P have been synthesized by solid phase and by the classical solution method. The modifications concerned all the C-terminal primary amide of SP and should therefore help to understand the biological significance of this carboxamide, as evaluated by in vivo and in vitro bioassays. From the results it can be seen that not the slightest change of the two amide protons is tolerated without an important loss of activity: replacement of one or two amide protons with alkyl groups, extension of the amide to the hydrazide and its alkyl analogues, and exchange of the amide with an ester or a carboxylic acid all reduce the relative activity/affinity at least by 2-fold. It is not clear for what reason all these modifications produce such a drastic activity reduction.

Groups of sea bass (Dicentrarhus labrax L.) were surgically implanted in the abdominal cavity with dialysis tubing of di¡erent pore size containing either live Photobacterium damsela subsp. piscicida cells or sterile phosphate-bu¡ered saline, in order to grow the pathogen in vivo. During the course of the experiment mortalities, not due to microbial infection, occurred, that prompted the use of histology in order to identify the lesions caused by molecules released from the dialysis bags during in vivo growth of the pathogen. Collected tissues from moribund ¢sh were processed for light microscopy. Fish implanted with the 2 kD molecular weight cut-o¡ (MWCO) bags suffered very minor histological changes whereas ¢sh with12 kD MWCO membranes showed severe lesions varying upon the time post operation. Moreover, in-£ammatory cells appeared in all tissues from ¢sh implanted with12 kD MWCO especially 48 h after infection. Spleen, liver, intestine and gills showed necrotic changes appearing 60 h post infection. Since no bacteria were isolated after microbiological sampling of tissue, the in£ammatory-necrotic changes observed in the tissues were attributed to the toxicity of extracellular products.