一个由17个微管相关基因组成的网络突出显示了乳腺癌中的功能性脱调
Sylvie Rodrigues-Ferreira1,2,3, Morgane Morin1,2, Gwenn Guichaoua4,5
1Gustave Roussy Cancer Center, F-94800 Villejuif, France.
Cancers
|October 14, 2023
概括
在乳腺癌中,与微管相关的基因被改变,影响患者的存活率. 准线性极光激酶为乳腺癌治疗提供了潜在的治疗策略.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- 微管相关的蛋白质和激酶调节细胞骨,并与癌症有关.
- 之前的一项研究确定了17个微管相关 (MT-Rel) 基因,在抗分类素的乳腺瘤中差异地表达.
研究的目的:
- 评估17个MT-Rel基因在乳腺癌中的表达,预后意义和功能影响.
- 在这些MT-Rel基因中识别潜在的治疗点.
主要方法:
- 对乳腺瘤与正常组织的基因表达分析.
- 使用患者生存数据进行预后价值评估.
- 系统生物学方法绘制功能网络的地图.
- 鉴定细胞生存必需的基因.
主要成果:
- 14个MT-Rel基因在乳腺瘤中被上调,其中6个过度表达>10倍.
- 四个MT-Rel基因 (KIF11,AURKB,TPX2,KIFC1) 对于细胞生存至关重要.
- 14个基因的过度表达和3个基因的不足表达与患者的生存率差相关.
- 确定了三种功能性网络,它们的中心是轴组装,染色体分离和细胞运动.
结论:
- 该研究确定了特定的MT-Rel基因作为乳腺癌预后的潜在生物标志物.
- 线性极光激酶及其基质代表了乳腺癌的有前途的治疗标.
相关概念视频
mTOR Signaling and Cancer Progression
3.8K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
The mTOR pathway or the...
3.8K
Destabilization of Microtubules
2.7K
The destabilization of microtubules can occur during different stages of the microtubule lifecycle, such as nucleation or elongation. It can take place at either end of the microtubule or in the microtubule lattices as a whole. The lifespan of individual microtubules within a cell varies according to the cell type and stage of the cell cycle. During interphase, the lifespan of the microtubule is about 30 minutes, while during cell division, it is about 15 minutes. In axonal microtubules of...
2.7K
Microtubule Instability
5.1K
Microtubules are hollow cylindrical filaments having a diameter of approximately 25 nm and a length that varies from 200 nm to 25 μm. GTP-bound tubulin subunits form αβ-heterodimers for microtubule assembly. These core building blocks interact longitudinally, polymerizing into protofilaments. The protofilaments then interact with one another through lateral bonding forces to form stable cylindrical microtubules. These cylindrical filaments are dynamic as they undergo repeated...
5.1K
Microtubule Formation
5.8K
Microtubules are dynamic structures that undergo continuous assembly and disassembly. They originate from specialized multi-protein complexes known as microtubule organizing centers or MTOCs. Within the MTOC, the point of origin of the microtubule is known as the minus end, while the end radiating outward is the plus end. Microtubules serve two primary functions — the organization of spindle complexes to separate sister chromatids during mitotic or meiotic cell division and the formation...
5.8K
Drugs that Destabilize Microtubules
2.0K
Microtubules are dynamic structures and can be regulated by microtubule targeting agents (MTAs). Microtubule destabilizing drugs are a class of MTAs that destabilize and prevent microtubules' polymerization. Both natural and synthetic chemicals can be found under this class of drugs. Vincristine and vinblastine, two vinca alkaloids, and colchicine were among the first to be discovered. These drugs can affect cells in various ways, either by inducing a change in cell morphology, preventing...
2.0K
Microtubules in Signaling
1.7K
The primary cilium, made up of microtubules, acts as antennae on the cell surfaces for relaying external stimuli into the cells. These fine hair-like structures are present, generally one per cell. These are non-motile cilia in a 9+0 microtubules arrangement, where the central pair of microtubules are absent. The primary cilia arise from the basal body embedded in the cell membrane. Intraflagellar transport (IFT) carries requisite proteins from the cytoplasm to the cilium because the primary...
1.7K


