Molecular design of hybrid tumour necrosis factor alpha with polyethylene glycol increases its anti-tumour potency.
This study was conducted to increase the anti-tumour potency and reduce the toxic side-effects of tumour necrosis factor alpha ( TNF-alpha). Natural human TNF-alpha was chemically conjugated with monomethoxy polyethylene glycol (PEG) using succinimidyl coupling of lysine amino groups of TNF-alpha. The number-average molecular weight of PEG-modified TNF-alpha (PEG- TNF-alpha) increased with an increase in the reaction time and the initial molar ratio of PEG relative to TNF-alpha. The resulting modified TNF-alpha was separated into fractions of various molecular weights. The specific activity of separated PEG- TNF-alpha s relative to that of native TNF-alpha gradually decreased with an increase in the degree of PEG modification, but the plasma half-life was drastically increased with the increase in molecular weight of modified TNF-alpha. PEG- TNF-alpha s, in which 29% and 56% of lysine residues were coupled to PEG, had anti-tumour activity approximately 4 and 100 times greater than unmodified TNF-alpha in the murine Meth-A fibrosarcoma model. Extensive PEG modification did not increase its in vivo activity. A high dose of unmodified TNF-alpha induced toxic side-effects, but these were not observed with the modified TNF-alpha s. Optimal PEG modification of TNF-alpha markedly increased its bioavailability and may facilitate its potential anti-tumour therapeutic use.[1]References
- Molecular design of hybrid tumour necrosis factor alpha with polyethylene glycol increases its anti-tumour potency. Tsutsumi, Y., Kihira, T., Tsunoda, S., Kanamori, T., Nakagawa, S., Mayumi, T. Br. J. Cancer (1995) [Pubmed]
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