Chapter 5 Immortalized Mouse Epithelial Cell Models to Study the Role of Apoptosis in Cancer

癌变 永生化细胞系 生物 癌症研究 癌症 细胞凋亡 细胞培养 细胞生物学 细胞 癌细胞 遗传学
作者
Robin Mathew,Kurt Degenhardt,Liti Haramaty,Cristina M. Karp,Eileen White
出处
期刊:Methods in Enzymology [Academic Press]
卷期号:: 77-106 被引量:28
标识
DOI:10.1016/s0076-6879(08)01605-4
摘要

Human cancer cell lines are widely used to model cancer but also have serious limitations. As an alternate approach, we have developed immortalized mouse epithelial cell model systems that are applicable to different tissue types and involve generation of immortalized cell lines that are genetically defined. By applying these model systems to mutant mice, we have extended the powerful approach of mouse genetics to in vitro analysis. By use of this model we have generated immortal epithelial cells that are either competent or deficient for apoptosis by different gain- and loss-of-function mutations that have revealed important mechanisms of tumor progression and treatment resistance. Furthermore, we have derived immortalized, isogenic mouse kidney, mammary, prostate, and ovarian epithelial cell lines to address the issues of tissue specificity. One of the major advantages of these immortalized mouse epithelial cell lines is the ability to perform biochemical analysis, screening, and further genetic manipulations. Moreover, the ability to generate tumor allografts in mice allows the integration of in vitro and in vivo approaches to delineate the mechanistic aspects of tumorigenesis. These model systems can be used effectively to determine the molecular requirements of epithelial tumorigenesis and tumor-promoting functions. This approach provides an efficient way to study the role of apoptosis in cancer and also enables the interrogation and identification of potential chemotherapeutic targets involving this pathway. Applying this technology to other mouse models can provide insight into additional aspects of oncogenesis.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
ruby完成签到,获得积分10
刚刚
青藤发布了新的文献求助10
1秒前
2秒前
冤家Gg发布了新的文献求助10
2秒前
luojinjin完成签到,获得积分10
3秒前
英吉利25发布了新的文献求助10
4秒前
5秒前
现代的东蒽完成签到,获得积分10
6秒前
seven7完成签到,获得积分10
6秒前
右二森关注了科研通微信公众号
7秒前
7秒前
一条咸鱼小辉辉完成签到,获得积分20
7秒前
8秒前
初景发布了新的文献求助30
8秒前
9秒前
11秒前
Jasper应助微笑的剑鬼采纳,获得10
11秒前
Sus发布了新的文献求助10
11秒前
12秒前
青藤完成签到,获得积分10
12秒前
爆米花应助合适幼荷采纳,获得10
13秒前
14秒前
beiwei完成签到 ,获得积分10
15秒前
BBridge发布了新的文献求助10
17秒前
17秒前
科研通AI6.4应助小北采纳,获得10
17秒前
18秒前
provin完成签到,获得积分10
18秒前
18秒前
王超完成签到,获得积分10
18秒前
21秒前
21秒前
hygge完成签到,获得积分10
22秒前
xiaoxiao完成签到,获得积分10
22秒前
22秒前
22秒前
22秒前
23秒前
23秒前
合适幼荷发布了新的文献求助10
24秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Molecular Mechanisms of Photosynthesis, 4th Edition 1000
Organic Reactions, Volume 116 1000
Current concepts in cutaneous toxicity : proceedings of the Fourth Conference on Cutaneous Toxicity, Washington, D.C., May 9-11, 1979 1000
The recovery-stress questionnaires : user manual 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7256332
求助须知:如何正确求助?哪些是违规求助? 8878360
关于积分的说明 18751270
捐赠科研通 6936509
什么是DOI,文献DOI怎么找? 3200809
关于科研通互助平台的介绍 2374982
邀请新用户注册赠送积分活动 2176400