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尿苷5'-二磷酸半乳糖:喂食N-(4-(5-硝基-2-呋喃基)-2-噻唑基)甲酰胺的大鼠脱落膀胱上皮细胞中的糖蛋白半乳糖基转移酶活性

Uridine 5'-diphosphate galactose: glycoprotein galactosyl transferase activity in exfoliated bladder epithelial cells in rats fed N-(4-(5-nitro-2-furyl)-2-thiazolyl) formamide.

作者信息

Plotkin G M, Brigham S C, Wolf G, Jacobs J B, Arai M

出版信息

Cancer Biochem Biophys. 1977;2(2):59-63.

PMID:99227
Abstract

Urine samples of normal male Fischer rats or rats fed 0.2% N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide for 6,8 or 30 weeks were collected and centrifuged 50 weeks after beginning treatment. After being sonicated and assayed (with purified desialylated ovine submaxillary mucin as acceptor glycoprotein), the exfoliated bladder cells obtained from the urines of treated rats showed uridine 5'-diphosphate galactose:glycoprotein transferase activity. The specific enzymatic activity of the enzyme from cells of 30-week-treated rats was about 10 times higher than from normal rats. The enzyme from cells of hyperplastic rats (treated 6 or 8 weeks) was only slightly higher in specific activity than that of normal rats. A similar was obtained at a later stage of bladder tumor induction, when the urines from 30-week-treated rats contained blood. A correction was made for protein contributed by the blood clot. The possibility that the blood clot contributed galactosyl transferase activity was excluded. Activity of the enzyme was detected in normal rat bladder tissue and in normal human urine.

摘要

收集正常雄性Fischer大鼠或喂食0.2% N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺6周、8周或30周的大鼠的尿液样本,并在开始治疗50周后进行离心。对处理过的大鼠尿液中获得的脱落膀胱细胞进行超声处理和检测(以纯化的去唾液酸羊颌下粘蛋白作为受体糖蛋白)后,显示出尿苷5'-二磷酸半乳糖:糖蛋白转移酶活性。处理30周的大鼠细胞中的该酶的比酶活性比正常大鼠高约10倍。增生大鼠(处理6周或8周)细胞中的酶的比活性仅略高于正常大鼠。在膀胱肿瘤诱导后期也得到了类似结果,此时处理30周的大鼠尿液中含有血液。对血凝块贡献的蛋白质进行了校正。排除了血凝块贡献半乳糖基转移酶活性的可能性。在正常大鼠膀胱组织和正常人尿液中检测到了该酶的活性。

相似文献

1
Uridine 5'-diphosphate galactose: glycoprotein galactosyl transferase activity in exfoliated bladder epithelial cells in rats fed N-(4-(5-nitro-2-furyl)-2-thiazolyl) formamide.尿苷5'-二磷酸半乳糖:喂食N-(4-(5-硝基-2-呋喃基)-2-噻唑基)甲酰胺的大鼠脱落膀胱上皮细胞中的糖蛋白半乳糖基转移酶活性
Cancer Biochem Biophys. 1977;2(2):59-63.
2
Galactosyl transferase activity in rat bladder transitional cell carcinoma lines and in exfoliated cells in urine during carcinogenesis and reversible hyperplasia.大鼠膀胱移行细胞癌系以及致癌过程和可逆性增生期间尿液中脱落细胞的半乳糖基转移酶活性
Cancer Biochem Biophys. 1980;4(4):251-6.
3
A long-term study of reversible and progressive urinary bladder cancer lesions in rats fed N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide.对喂食N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺的大鼠膀胱可逆性和进展性癌病变的长期研究。
Cancer Res. 1977 Aug;37(8 Pt 2):2817-21.
4
Effect of dose on urinary bladder carcinogenesis induced in F344 rats by N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide.剂量对N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺诱导F344大鼠膀胱致癌作用的影响。
J Natl Cancer Inst. 1979 Apr;62(4):1013-6.
5
Aspirin inhibition of N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide-induced lesions of the urinary bladder correlated with inhibition of metabolism by bladder prostaglandin endoperoxide synthetase.阿司匹林对N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺诱导的膀胱损伤的抑制作用与膀胱前列腺素内过氧化物合成酶对其代谢的抑制作用相关。
Cancer Res. 1981 Sep;41(9 Pt 1):3355-9.
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Neovascularization in rats during urinary bladder carcinogenesis induced by N-[4-(5-Nitro-2-furyl)-2-thiazolyl]formamide.N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺诱导大鼠膀胱致癌过程中的新生血管形成
J Natl Cancer Inst. 1980 Jul;65(1):145-8.
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Effect of aspirin on urinary bladder carcinogenesis initiated with N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide in rats.阿司匹林对N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺诱发大鼠膀胱癌的影响。
Cancer Res. 1989 Jan 15;49(2):372-7.
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Effect of sodium phenobarbital and sodium saccharin in AIN-76A diet on carcinogenesis initiated with N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide and N,N-dibutylnitrosamine in male F344 rats.苯巴比妥钠和糖精钠在AIN - 76A饮食中对雄性F344大鼠由N - [4 -(5 - 硝基 - 2 - 呋喃基)- 2 - 噻唑基]甲酰胺和N,N - 二丁基亚硝胺引发的致癌作用的影响。
Cancer Res. 1986 Dec;46(12 Pt 1):6160-4.
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Promoting effect of saccharin and DL-tryptophan in urinary bladder carcinogenesis.糖精和DL-色氨酸在膀胱癌发生中的促进作用。
Cancer Res. 1979 Apr;39(4):1207-17.
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Low susceptibility of analbuminemic rats to induction of bladder cancer by N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide.无白蛋白血症大鼠对N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺诱导膀胱癌的低易感性。
Jpn J Cancer Res. 1985 Jul;76(7):577-82.