相关实验视频
Updated: Apr 26, 2026

09:45
Detection of Copy Number Alterations Using Single Cell Sequencing
Published on: February 17, 2017
12.6K
乳腺癌的克隆进化是由单核基因组测序揭示的
Yong Wang1, Jill Waters1, Marco L Leung2
1The University of Texas MD Anderson Cancer Center, Department of Genetics, Houston, Texas 77030, USA.
Nature
|August 1, 2014
概括
这项研究介绍了nuc-seq,这是一种用于乳腺癌的新型单细胞测序方法. 它揭示了早期的,稳定的动体积和渐进的点突变演变,影响了癌症治疗策略.
科学领域:
- 基因组学就是基因组学.
- 癌症生物学 癌症生物学
- 分子瘤学分子瘤学
背景情况:
- 现有的乳腺癌测序研究对瘤内基因组多样性的洞察力有限.
- 了解瘤进化和异质性对于有效的癌症治疗至关重要.
研究的目的:
- 开发和应用一种新的全基因组和外体单细胞测序方法 (nuc-seq) 来分析乳腺瘤中的基因组多样性.
- 研究不同乳腺癌亚型的拷贝数变化和点突变的进化动态.
主要方法:
- 开发了nuc-seq,一种全基因组和外体单细胞测序方法,利用G2/M核进行高覆盖.
- 应用 nuc-seq 单个核从ER (((+) 乳腺癌和三阴性导管癌.
- 进行单核复制号分析和向单分子测序.
主要成果:
- 在瘤克隆扩张期间,状重组是早期和稳定的.
- 点突变逐渐演变,产生显著的克隆多样性,通常在低频率 (<10%).
- 三重阴性瘤的突变率比ER瘤增加了13.3倍.
结论:
- Nuc-seq提供了对乳腺癌基因组异质性的深入了解.
- 早期的状体稳定性和逐渐的点突变积累塑造了瘤的进化.
- 乳腺癌亚型的突变率差异对诊断和治疗有影响.
相关概念视频
Cancers Originate from Somatic Mutations in a Single Cell
12.4K
Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
12.4K
Cancers Originate from Somatic Mutations in a Single Cell
3.1K
3.1K
Evolutionary Relationships through Genome Comparisons
5.8K
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
5.8K
The Nucleolus
8.6K
The nucleolus is the most prominent substructure of the nucleus. When it was first discovered, it was considered to be an isolated organelle that forms fibrils and granules. In 1931, the relationship between the nucleolus and chromosomes was first described by Heitz. He observed that the appearance and size of nucleolus varies depending on the stage of the cell cycle. He also noticed constricted regions on different chromosomes clustered together at definite cell cycle stages. These regions,...
8.6K
Next-generation Sequencing
87.6K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
87.6K
Cancer-Critical Genes II: Tumor Suppressor Genes
2.6K
2.6K

