Luk G D, Canellakis Z N
Department of Medicine, Wayne State University School of Medicine, Detroit, Michigan 48201.
Biochem Int. 1990;20(1):169-76.
Our studies demonstrate that diacetylputrescine (TMBA), and its analog hexamethylenebisacetamide, HMBA, inhibit the expression of the c-myc oncogene in activated human B-lymphocytes. Activation of human B-cells induced by anti-IgM is associated with the induction of c-myc by greater than 20 times basal levels, maximal levels occurring at about 2 hours. This increased c-myc expression is inhibited by greater than 90% by 3 mM TMBA or 3mM HMBA. TMBA and HMBA also inhibit by greater than 90% the subsequent activation of the B-cells. These diacetylated polyamines may play a regulatory role in B-cell activation.
我们的研究表明,二乙酰腐胺(TMBA)及其类似物六亚甲基双乙酰胺(HMBA)可抑制活化的人B淋巴细胞中c-myc癌基因的表达。抗IgM诱导的人B细胞活化与c-myc的诱导有关,其水平比基础水平高20倍以上,最高水平出现在约2小时。3 mM TMBA或3 mM HMBA可将这种c-myc表达的增加抑制90%以上。TMBA和HMBA还可将随后的B细胞活化抑制90%以上。这些二乙酰化多胺可能在B细胞活化中起调节作用。