Dráber Pavel, Dráberová Eduarda
Department of Biology of Cytoskeleton, Institute of Molecular Genetics, Czech Academy of Sciences, CZ-142 20 Prague, Czech Republic.
Cancers (Basel). 2021 Nov 11;13(22):5638. doi: 10.3390/cancers13225638.
In cells, microtubules typically nucleate from microtubule organizing centers, such as centrosomes. γ-Tubulin, which forms multiprotein complexes, is essential for nucleation. The γ-tubulin ring complex (γ-TuRC) is an efficient microtubule nucleator that requires additional centrosomal proteins for its activation and targeting. Evidence suggests that there is a dysfunction of centrosomal microtubule nucleation in cancer cells. Despite decades of molecular analysis of γ-TuRC and its interacting factors, the mechanisms of microtubule nucleation in normal and cancer cells remains obscure. Here, we review recent work on the high-resolution structure of γ-TuRC, which brings new insight into the mechanism of microtubule nucleation. We discuss the effects of γ-TuRC protein dysregulation on cancer cell behavior and new compounds targeting γ-tubulin. Drugs inhibiting γ-TuRC functions could represent an alternative to microtubule targeting agents in cancer chemotherapy.
在细胞中,微管通常从微管组织中心(如中心体)成核。形成多蛋白复合物的γ-微管蛋白对成核至关重要。γ-微管蛋白环复合物(γ-TuRC)是一种高效的微管成核剂,其激活和靶向需要额外的中心体蛋白。有证据表明癌细胞中存在中心体微管成核功能障碍。尽管对γ-TuRC及其相互作用因子进行了数十年的分子分析,但正常细胞和癌细胞中微管成核的机制仍不清楚。在这里,我们综述了关于γ-TuRC高分辨率结构的最新研究,这为微管成核机制带来了新的见解。我们讨论了γ-TuRC蛋白失调对癌细胞行为的影响以及靶向γ-微管蛋白的新化合物。抑制γ-TuRC功能的药物可能成为癌症化疗中微管靶向药物的替代品。