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1
Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activity.氟尿苷诱导的脆性(X)表达是短暂的,且与胸苷酸合成酶活性水平呈负相关。
Am J Hum Genet. 1985 Sep;37(5):947-55.
2
Variability of thymidylate synthase activity in whole blood cultures treated with FUdR.用氟尿苷处理的全血培养物中胸苷酸合成酶活性的变异性。
Am J Med Genet. 1986 Jan-Feb;23(1-2):483-90. doi: 10.1002/ajmg.1320230140.
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Fragile X expression increased by low cell-culture density.
Am J Med Genet. 1986 Jan-Feb;23(1-2):467-73. doi: 10.1002/ajmg.1320230138.
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The effect of caffeine on fragile X expression.咖啡因对脆性X表达的影响。
Hum Genet. 1986 May;73(1):20-2. doi: 10.1007/BF00292657.
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Thymidylate synthase mRNA expression does not predict resistance to floxuridine in a choriocarcinoma cell line.胸苷酸合成酶mRNA表达不能预测绒毛膜癌细胞系对氟尿苷的耐药性。
J Reprod Med. 2010 May-Jun;55(5-6):247-52.
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Antisense-induced down-regulation of thymidylate synthase and enhanced cytotoxicity of 5-FUdR in 5-FUdR-resistant HeLa cells.反义诱导胸苷酸合成酶下调及5-氟脱氧尿苷对5-氟脱氧尿苷耐药的HeLa细胞增强的细胞毒性作用
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[Establishment of floxuridine-resistant JeG-3 subline and the role of thymidylate synthetase mRNA expression in chem-resistant-prediction.].
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Cytogenetic investigations in mentally retarded and normal males from 14 families with the fragile site at Xq28. Results of folic acid treatment on fra(X) expression.对14个家系中具有Xq28脆性位点的智力迟钝男性和正常男性进行的细胞遗传学研究。叶酸治疗对fra(X)表达的影响结果。
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The fragile X(q27) form of X-linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes.
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HPV16-E7 expression causes fluorodeoxyuridine-mediated radiosensitization in SW620 human colon cancer cells.人乳头瘤病毒16型E7蛋白的表达使SW620人结肠癌细胞对氟脱氧尿苷介导的放射增敏。
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本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Cell cycle regulation of thymidylate synthetase gene expression in cultured mouse fibroblasts.培养的小鼠成纤维细胞中胸苷酸合成酶基因表达的细胞周期调控
J Biol Chem. 1980 Aug 10;255(15):7386-90.
3
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: a new technical approach.脆性X染色体在淋巴细胞和成纤维细胞培养中的表达:一种新的技术方法。
Hum Genet. 1981;59(2):166-9. doi: 10.1007/BF00293069.
4
X-linked mental retardation: a study of 7 families.X连锁智力迟钝:对7个家族的研究
Am J Med Genet. 1980;7(4):471-89. doi: 10.1002/ajmg.1320070408.
5
X-linked mental retardation, macro-orchidism, and the Xq27 fragile site.X连锁智力迟钝、巨睾症与Xq27脆性位点
J Pediatr. 1980 May;96(5):837-41. doi: 10.1016/s0022-3476(80)80552-x.
6
The expression of fragile X chromosomes in members of the same family at different times of examination.
Hum Genet. 1982;61(3):254-5. doi: 10.1007/BF00296453.
7
Marker X syndrome in an oriental family with probable transmission by a normal male.一个东方家庭中的标记X综合征,可能由一名正常男性遗传。
Am J Med Genet. 1982 Jun;12(2):205-17. doi: 10.1002/ajmg.1320120211.
8
Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).X连锁智力迟钝与X染色体标记fra(X)(q27)的杂合表达。
N Engl J Med. 1980 Sep 18;303(12):662-4. doi: 10.1056/NEJM198009183031202.
9
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.脆性X智力障碍综合征与乙型血友病紧密连锁并通过正常男性传递。
Nature. 1983;306(5944):701-4. doi: 10.1038/306701a0.
10
Marker X chromosome induction in fibroblasts by FUdR.氟尿苷(FUdR)诱导成纤维细胞中X染色体标记
Am J Med Genet. 1981;9(3):263-4. doi: 10.1002/ajmg.1320090313.

氟尿苷诱导的脆性(X)表达是短暂的,且与胸苷酸合成酶活性水平呈负相关。

Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activity.

作者信息

Cantú E S, Nussbaum R L, Airhart S D, Ledbetter D H

出版信息

Am J Hum Genet. 1985 Sep;37(5):947-55.

PMID:2931977
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1684697/
Abstract

Thymidylate synthase (TS) activity was monitored in fluorodeoxyuridine (FUdR)-treated lymphoblasts from individuals carrying the fragile (X) [fra(X)] chromosome. Fra(X) expression and levels of TS activity were measured over a 72-hr period at different cell densities. TS activity was 80%-90% inhibited immediately after exposure to FUdR and remained suppressed for the first 24 hrs. Fra(X) expression was not found until 6-8 hrs after FUdR treatment, and at 24 hrs, reached a maximum expression of approximately 50%. At 48 and 72 hrs, however, increasing levels of TS activity paralleled a dramatic drop in fra(X) expression. High fra(X) expression at 48 and 72 hrs could be maintained by rechallenging cultures with increasing doses of FUdR. At low cell densities, fra(X) expression was maintained at high levels for a much longer period of time. In two lymphoblastoid cell lines from obligate carriers, which either expressed at very low levels or did not express the fra(X) in routine cultures, TS activity was also 90% inhibited but with no corresponding fra(X) expression 12 or 24 hrs after FUdR treatment. We conclude that: FUdR inhibits TS activity immediately and induces fra(X) expression 6-8 hrs later, FUdR-induced fra(X) expression and TS activity are inversely related, the FUdR effect on fra(X) expression and TS activity is time and cell-density dependent, and inhibition of TS activity is a necessary but not sufficient condition for fra(X) expression.

摘要

在来自携带脆性X染色体[fra(X)]个体的经氟脱氧尿苷(FUdR)处理的淋巴母细胞中监测胸苷酸合成酶(TS)活性。在不同细胞密度下,在72小时内测量fra(X)表达和TS活性水平。暴露于FUdR后,TS活性立即被抑制80%-90%,并在最初24小时内保持受抑制状态。直到FUdR处理后6-8小时才发现fra(X)表达,在24小时时,达到约50%的最大表达。然而,在48和72小时时,TS活性水平的增加与fra(X)表达的急剧下降平行。通过用增加剂量的FUdR再次刺激培养物,可以在48和72小时维持高fra(X)表达。在低细胞密度下,fra(X)表达在更长时间内维持在高水平。在来自 obligate携带者的两个淋巴母细胞系中,它们在常规培养中要么表达水平非常低,要么不表达fra(X),在FUdR处理后12或24小时,TS活性也被抑制90%,但没有相应的fra(X)表达。我们得出结论:FUdR立即抑制TS活性,并在6-8小时后诱导fra(X)表达;FUdR诱导的fra(X)表达与TS活性呈负相关;FUdR对fra(X)表达和TS活性的影响取决于时间和细胞密度;TS活性的抑制是fra(X)表达的必要但不充分条件。