Glebov A V, Kalinovskiĭ V P, Seĭts I F
Eksp Onkol. 1986;8(6):16-8.
Pepsinogen mRNA is shown to be the major fraction of rat poly (A)+RNA. It codes polypeptide with molecular weight of about 45 kD. Changes in the pepsinogen mRNA content at the early stage of carcinogenesis are nonspecific and are due to the toxic effect of MNNG. Steady shifts in the quantity of pepsinogen mRNA are found between the 1st and 3d months. Pepsinogen mRNA content decreases down to the half of the normal one between the 3d and 6th months. A quantity of RNA capable to be a template for pepsinogen synthesis is reduced by more than 90% in the MNNG induced tumour. The pepsinogen production defect in gastric mucosa neoplasia is mainly due to pepsinogen mRNA synthesis damage.
胃蛋白酶原mRNA被证明是大鼠多聚腺苷酸(poly (A)+)RNA的主要成分。它编码分子量约为45kD的多肽。在致癌作用早期,胃蛋白酶原mRNA含量的变化是非特异性的,是由N-甲基-N'-硝基-N-亚硝基胍(MNNG)的毒性作用引起的。在第1个月和第3个月之间发现胃蛋白酶原mRNA数量有稳定变化。在第3个月和第6个月之间,胃蛋白酶原mRNA含量降至正常水平的一半。在MNNG诱导的肿瘤中,能够作为胃蛋白酶原合成模板的RNA数量减少了90%以上。胃黏膜肿瘤形成中胃蛋白酶原产生缺陷主要是由于胃蛋白酶原mRNA合成受损。