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线粒体相关嘧啶合成的部分抑制会增加致瘤潜力和溶酶体积累。

Partial inhibition of mitochondrial-linked pyrimidine synthesis increases tumorigenic potential and lysosome accumulation.

作者信息

Desler Claus, Durhuus Jon Ambæk, Hansen Thomas Lau-Lindestrand, Anugula Sharath, Zelander Nadia Thaulov, Bøggild Sisse, Rasmussen Lene Juel

机构信息

Center for Healthy Aging, Department of Cellular and Molecular Medicine, University of Copenhagen, Denmark.

Center for Healthy Aging, Department of Cellular and Molecular Medicine, University of Copenhagen, Denmark; Department of Clinical Research, Copenhagen University Hospital - Amager and Hvidovre, Copenhagen, Denmark.

出版信息

Mitochondrion. 2022 May;64:73-81. doi: 10.1016/j.mito.2022.03.005. Epub 2022 Mar 25.

Abstract

The correlation between mitochondrial function and oncogenesis is complex and is not fully understood. Here we determine the importance of mitochondrial-linked pyrimidine synthesis for the aggressiveness of cancer cells. The enzyme dihydroorotate dehydrogenase (DHODH) links oxidative phosphorylation to de novo synthesis of pyrimidines. We demonstrate that an inhibition of DHODH results in a respiration-independent significant increase of anchorage-independent growth but does not affect DNA repair ability. Instead, we show an autophagy-independent increase of lysosomes. The results of this study suggest that inhibition of mitochondrial-linked pyrimidine synthesis in cancer cells results in a more aggressive tumor phenotype.

摘要

线粒体功能与肿瘤发生之间的相关性很复杂,尚未完全了解。在此,我们确定了线粒体相关嘧啶合成对癌细胞侵袭性的重要性。二氢乳清酸脱氢酶(DHODH)将氧化磷酸化与嘧啶的从头合成联系起来。我们证明,抑制DHODH会导致不依赖于呼吸作用的锚定非依赖性生长显著增加,但不影响DNA修复能力。相反,我们发现溶酶体在不依赖自噬的情况下增加。本研究结果表明,抑制癌细胞中线粒体相关的嘧啶合成会导致更具侵袭性的肿瘤表型。

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