Selective PI3K inhibition by BKM120 and BEZ235 alone or in combination with chemotherapy in wild-type and mutated human gastrointestinal cancer cell lines.
第一作者:
Annett,Mueller
第一单位:
First Department of Internal Medicine, University Medical Centre of the Johannes Gutenberg University Mainz, Langenbeckstrasse 1, 55101, Mainz, Germany. annett.mueller@unimedizin-mainz.de
作者:
主题词
氨基吡啶类(Aminopyridines);抗肿瘤联合化疗方案(Antineoplastic Combined Chemotherapy Protocols);喜树碱(Camptothecin);半胱氨酸天冬氨酸蛋白酶3(Caspase 3);细胞存活(Cell Survival);剂量效应关系, 药物(Dose-Response Relationship, Drug);胃肠肿瘤(Gastrointestinal Neoplasms);HCT116细胞(HCT116 Cells);HT29细胞(HT29 Cells);人类(Humans);咪唑类(Imidazoles);吗啉类(Morpholines);突变(Mutation);蛋白激酶抑制剂(Protein Kinase Inhibitors);原癌基因蛋白质c-akt(Proto-Oncogene Proteins c-akt);喹啉类(Quinolines);信号传导(Signal Transduction);TOR丝氨酸-苏氨酸激酶(TOR Serine-Threonine Kinases)
DOI
10.1007/s00280-012-1869-z
PMID
22543857
发布时间
2021-12-03
- 浏览49
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文