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鸟氨酸脱羧酶在表皮肿瘤发生中的作用。

Role of ornithine decarboxylase in epidermal tumorigenesis.

作者信息

Clifford A, Morgan D, Yuspa S H, Soler A P, Gilmour S

机构信息

Lankenau Medical Research Center, Wynnewood, Pennsylvania 19096, USA.

出版信息

Cancer Res. 1995 Apr 15;55(8):1680-6.

PMID:7712475
Abstract

Ornithine decarboxylase (ODC) plays a key role in the biosynthesis of polyamines, which are necessary for cell growth and differentiation. ODC expression is very tightly controlled in all normal cells; however, regulation of its expression is altered in many tumor cells resulting in much higher basal levels of ODC in tumors. To investigate the potential role of ODC overexpression in epidermal tumorigenesis, we constructed a replication-defective retroviral vector to overexpress a truncated ODC protein in epidermal cells. Stable viral infection of mouse epidermal cells dramatically increases not only the basal ODC activity but also the basal putrescine and spermidine levels. In all infected epidermal cells with high polyamine levels, DNA synthesis is increased as measured by [3H]thymidine incorporation into DNA as well as increased bromodeoxyuridine staining in the nuclei of ODC-infected epidermal cells. ODC viral infection of nontumorigenic BK-1 epidermal cells and primary cultures of mouse keratinocytes and fibroblasts from newborn mouse skin yields no tumors when injected s.c. into athymic nude mice or when transplanted as skin grafts onto nude mice. Epidermal cell lines SP-1 and 308 (which possess an activated rasHa gene) are not tumorigenic when injected s.c. into nude mice. However, following infection with the ODC virus, they form tumors filled with keratin and papilloma-like projections of hyperplastic epidermal cells displaying dysplasia and many mitotic figures. These data indicate that ODC overexpression by itself is not sufficient to induce tumors in normal cells but that increased expression of ODC enhances tumor development in initiated premalignant epidermal cells.

摘要

鸟氨酸脱羧酶(ODC)在多胺的生物合成中起关键作用,多胺是细胞生长和分化所必需的。ODC的表达在所有正常细胞中受到非常严格的调控;然而,其表达的调控在许多肿瘤细胞中发生改变,导致肿瘤中ODC的基础水平高得多。为了研究ODC过表达在表皮肿瘤发生中的潜在作用,我们构建了一种复制缺陷型逆转录病毒载体,以在表皮细胞中过表达截短的ODC蛋白。小鼠表皮细胞的稳定病毒感染不仅显著增加了基础ODC活性,还增加了基础腐胺和亚精胺水平。在所有多胺水平高的感染表皮细胞中,通过将[3H]胸苷掺入DNA来测量的DNA合成增加,以及ODC感染的表皮细胞核中溴脱氧尿苷染色增加。将非致瘤性BK-1表皮细胞、新生小鼠皮肤的小鼠角质形成细胞和成纤维细胞的原代培养物进行ODC病毒感染后,皮下注射到无胸腺裸鼠中或作为皮肤移植物移植到裸鼠身上时均未产生肿瘤。表皮细胞系SP-1和308(具有激活的rasHa基因)皮下注射到裸鼠中时不具有致瘤性。然而,在用ODC病毒感染后,它们形成充满角蛋白的肿瘤以及增生性表皮细胞的乳头状瘤样突起,显示发育异常和许多有丝分裂象。这些数据表明,ODC自身过表达不足以在正常细胞中诱导肿瘤,但ODC表达增加会增强起始的癌前表皮细胞中的肿瘤发展。

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