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通过调控微量金属元素来控制白血病细胞(L1210)的生长

Control of the growth of leukemic cells (L1210) through manipulation of trace metals.

作者信息

Oblender M, Carpentieri U

机构信息

Department of Pediatrics, UTMB, Galveston, TX 77550.

出版信息

Anticancer Res. 1991 Jul-Aug;11(4):1561-4.

PMID:1746914
Abstract

Trace metals have a role in the activity of the enzyme ribonucleotide reductase (RR) which is essential for the synthesis of DNA and the growth of lymphocytes. Manipulation of the intracellular metals of leukemic cells has been proposed for the therapeutic control of cell growth. We studied the effects of prolonged metal deprivation (Fe, Cu, Zn) on cell growth and RR activity of murine leukemic lymphocytes in culture in metal-depleted media. Intracellular metals, cell growth and RR activity were decreased in related and interdependent ways. A metal-chelator (deferoxamine, DFX) had similar effect. In all cases these effects were reversible by metal supplementation. We conclude that it is possible to control RR activity and growth of leukemic cells in vitro by exposing them to a metal-poor environment (eg. through the action of a chelator). These effects are not permanent, but might be beneficial if integrated with more conventional measures (chemotherapy).

摘要

微量金属在核糖核苷酸还原酶(RR)的活性中发挥作用,该酶对于DNA合成和淋巴细胞生长至关重要。有人提出通过操纵白血病细胞的细胞内金属来治疗性控制细胞生长。我们研究了在贫金属培养基中长时间金属剥夺(铁、铜、锌)对培养的小鼠白血病淋巴细胞的细胞生长和RR活性的影响。细胞内金属、细胞生长和RR活性以相关且相互依赖的方式降低。一种金属螯合剂(去铁胺,DFX)具有类似的效果。在所有情况下,这些影响通过补充金属均可逆转。我们得出结论,通过将白血病细胞暴露于贫金属环境(例如通过螯合剂的作用),有可能在体外控制RR活性和白血病细胞的生长。这些影响不是永久性的,但如果与更传统的措施(化疗)相结合可能会有益。

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