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内源性γ-干扰素激活结直肠癌组织中的胸苷磷酸化酶。

Endogenous gamma-interferon activates thymidine phosphorylase in colorectal cancer tissue.

作者信息

Iwagaki H, Hizuta A, Mori K, Yoshino T, Kawahara K, Tanaka N, Orita K

机构信息

First Department of Surgery, Okayama University Medical School, Japan.

出版信息

Res Commun Mol Pathol Pharmacol. 1995 Mar;87(3):345-52.

PMID:7620827
Abstract

We measured neopterin (NPT), an indirect marker of gamma (gamma)-interferon, and the activity of thymidine phosphorylase (dThdPase) in the advancing front of colorectal carcinoma and in normal mucosa. Cancer showed a higher concentration of NPT than normal mucosa and also showed significantly higher (p < 0.0001) dThdPase activity than normal mucosa. There was a strong correlation between NPT concentration and dThdPase activity in cancerous and normal mucosa. These results suggest that endogenous gamma-interferon could activate dThdPase activity, which is essential to nucleic acid metabolism because it regulates the availability of thymidine.

摘要

我们测定了新蝶呤(NPT),一种γ-干扰素的间接标志物,以及在结直肠癌进展前沿和正常黏膜中胸苷磷酸化酶(dThdPase)的活性。癌症组织中NPT的浓度高于正常黏膜,并且dThdPase活性也显著高于正常黏膜(p < 0.0001)。癌组织和正常黏膜中NPT浓度与dThdPase活性之间存在强相关性。这些结果表明,内源性γ-干扰素可激活dThdPase活性,而dThdPase活性对核酸代谢至关重要,因为它调节胸苷的可用性。

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