吉西他滨
胰腺癌
表皮生长因子受体
癌症研究
癌细胞
适体
癌症
酪氨酸激酶
药理学
受体酪氨酸激酶
化学
生物
受体
医学
激酶
细胞生物学
分子生物学
内科学
生物化学
作者
Partha Ray,Marcus A. Cheek,Mariam L. Sharaf,Na Li,Andrew D. Ellington,Bruce A. Sullenger,Barbara Ramsay Shaw,Rebekah R. White
出处
期刊:Nucleic Acid Therapeutics
[Mary Ann Liebert]
日期:2012-10-01
卷期号:22 (5): 295-305
被引量:68
标识
DOI:10.1089/nat.2012.0353
摘要
Gemcitabine is a nucleoside analog that is currently the best available single-agent chemotherapeutic drug for pancreatic cancer. However, efficacy is limited by our inability to deliver sufficient active metabolite into cancer cells without toxic effects on normal tissues. Targeted delivery of gemcitabine into cancer cells could maximize effectiveness and concurrently minimize toxic side effects by reducing uptake into normal cells. Most pancreatic cancers overexpress epidermal growth factor receptor (EGFR), a trans-membrane receptor tyrosine kinase. We utilized a nuclease resistant RNA aptamer that binds and is internalized by EGFR on pancreatic cancer cells to deliver gemcitabine-containing polymers into EGFR-expressing cells and inhibit cell proliferation in vitro. This approach to cell type–specific therapy can be adapted to other targets and to other types of therapeutic cargo.
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