癌症细胞中另一种形式的修饰的高活性6-磷酸果糖-1-激酶

A. Kristl, K. Čamernik, S. Avbelj, M. Legiša
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引用次数: 1

摘要

糖酵解通量增加是癌症细胞的一个特征。糖酵解的关键调节酶6-磷酸果糖-1-激酶(Pfk1)的翻译后修饰可能引发代谢通量失调。在癌症细胞中,人85kDa肌肉型nPfk-M酶可以被蛋白水解切割以形成高活性的47kDa短片段,其保持活性但对反馈抑制具有抗性。在几种致瘤细胞系中,也没有发现天然的85kDa肝型nPfk-L亚型,并且通过免疫印迹仅检测到70kDa的较短片段。为了了解更多关于癌症特异性修饰的sfPfk-L酶的信息,将编码70kDa片段的截短的人sfPfk-L基因插入无pfk酵母酿酒酵母细胞中。相对于重组天然PFK-L酶,重组修饰酶对底物果糖-6-磷酸表现出更高的亲和力,对柠檬酸盐和ATP抑制的敏感性降低。相对于四聚体天然nPfk-L酶,在缓冲液中稀释的条件下,缺乏酶的C部分的部分纯化的癌症特异性sfPfk-L片段显示出一些不稳定性。编码短sfPfk-L酶的酵母转化体的生长特性类似于编码短sfPfk-M酶的那些。在葡萄糖上没有观察到具有sfPfk-L基因的转化体的生长,但在培养基中具有低麦芽糖浓度和10mM乙醇的狭窄生态位中,它比具有天然人nPfk-L酶的转化体生长得更快。类似于修饰的47kDa sfPfk-M片段,短的70kDa nPfk-L片段也可能导致酵母和癌症细胞中糖酵解通量的失调。在酵母中,失调的代谢通量使氧化还原电位失衡,从而导致生长速度降低。然而,癌症细胞通过快速再氧化多余的NADH来克服氧化还原失衡,这导致乳酸盐的形成,而生长速率仍然很高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Another Form of Modified, Highly-Active 6-Phosphofructo-1-Kinase in Cancer Cells
Enhanced glycolytic flux is a hallmarks of cancer cells. Posttranslational modification of the key regulatory enzyme of glycolysis, 6-Phosphofructo-1- Kinase (Pfk1) might trigger metabolic flux deregulation. In the cancer cells the human 85 kDa muscle type nPfk-M enzyme can be proteolytically cleaved to form highly-active 47 kDa shorter fragments that retain activity but become resistant to feed-back inhibition. In several tumorigenic cell lines, no native 85 kDa liver type nPfk-L isoforms could be either found and only 70 kDa shorter fragments were detected by immune-blotting. To learn more about the cancer-specific modified sfPfk-L enzyme, the truncated human sfPfk-L gene encoding 70 kDa fragments was inserted into the pfk null yeast S.cerevisiae cell. The recombinant modified enzyme showed higher affinity toward the substrate fructose-6-phosphate, reduced sensitivity toward the citrate and ATP inhibition in respect to the recombinant native PFK-L enzyme. Partially purified cancer-specific sfPfk-L fragments lacking the C-portion of the enzyme showed some instability under the diluted conditions in the buffer in respect to the tetrameric native nPfk-L enzyme. Growth characteristics of the yeast transformant encoding short sfPfk-L enzymes were similar to those encoding shorter sfPfk-M enzymes. No growth of the transformant with the sfPfk-L gene was observed on glucose but it grew faster than the transformant with the native human nPfk-L enzyme in a narrow ecological niche with low maltose concentration and 10 mM of ethanol in the medium. Similar to modified 47 kDa sfPfk-M fragments, also the short 70 kDa nPfk- Lfragments might cause deregulation of the glycolytic flux in the yeast and in the cancer cells. In yeast, deregulated metabolic flux unbalances redox potential that results in reduced growth rate. However, the cancer cells beat the redox unbalance by rapid re-oxidation of redundant NADH that results in lactate formation while the growth rate remains high.
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