生物合成
乳腺癌
干细胞
胆固醇
钥匙(锁)
癌症
内科学
癌症研究
肿瘤科
医学
生物
内分泌学
生物信息学
生物化学
细胞生物学
基因
生态学
作者
Sidse Ehmsen,Martin H. Pedersen,Guisong Wang,Mikkel G. Terp,Amina Arslanagic,Brian L. Hood,Thomas P. Conrads,Rikke Leth‐Larsen,Henrik J. Ditzel
出处
期刊:Cell Reports
[Cell Press]
日期:2019-06-01
卷期号:27 (13): 3927-3938.e6
被引量:175
标识
DOI:10.1016/j.celrep.2019.05.104
摘要
Tumor eradication may be greatly improved by targeting cancer stem cells (CSCs), as they exhibit resistance to conventional therapy. To gain insight into the unique biology of CSCs, we developed patient-derived xenograft tumors (PDXs) from ER- breast cancers from which we isolated mammospheres that are enriched for CSCs. Comparative global proteomic analysis was performed on patient tumor tissues and corresponding PDXs and mammospheres. Mammospheres exhibited increased expression of proteins associated with de novo cholesterol synthesis. The clinical relevance of increased cholesterol biosynthesis was verified in a large breast cancer cohort showing correlation with shorter relapse-free survival. RNAi and chemical inhibition of the cholesterol biosynthesis pathway reduced mammosphere formation, which could be rescued by a downstream metabolite. Our findings identify the cholesterol biosynthesis pathway as central for CSC propagation and a potential therapeutic target, as well as providing a mechanistic explanation for the therapeutic benefit of statins in breast cancer.
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