4.8 Article

Identification of potential anticancer drug targets through the selection of growth-inhibitory genetic suppressor elements

期刊

CANCER CELL
卷 4, 期 1, 页码 41-53

出版社

CELL PRESS
DOI: 10.1016/S1535-6108(03)00169-7

关键词

-

资金

  1. NCI NIH HHS [R01 CA95727, R01 CA62099, R21 CA76908] Funding Source: Medline

向作者/读者索取更多资源

To identify human genes required for tumor cell growth, transcriptome-scale selection was used to isolate genetic suppressor elements (GSEs) inhibiting breast carcinoma cell growth. Growth-inhibitory GSEs (cDNA fragments that counteract their cognate gene) were selected from 57 genes, including known positive regulators of cell growth or carcinogenesis as well as genes that have not been previously implicated in cell proliferation. Many GSE-cognate genes encode transcription factors (such as STAT and AP-1) and signal transduction proteins. Monoclonal antibodies against a cell surface protein identified by GSE selection, neural cell adhesion molecule L1CAM, strongly inhibited the growth of several tumor cell lines but not of untransformed cells. Hence, selection for growth-inhibitory GSEs allows one to find potential targets for new anticancer drugs.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据