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吉西他滨与CHK1抑制剂联合治疗可诱导富集于非小细胞肺癌细胞系肿瘤球状体中的癌症干细胞样细胞产生凋亡抗性。

Combined gemcitabine and CHK1 inhibitor treatment induces apoptosis resistance in cancer stem cell-like cells enriched with tumor spheroids from a non-small cell lung cancer cell line.

作者信息

Fang Douglas D, Cao Joan, Jani Jitesh P, Tsaparikos Konstantinos, Blasina Alessandra, Kornmann Jill, Lira Maruja E, Wang Jianying, Jirout Zuzana, Bingham Justin, Zhu Zhou, Gu Yin, Los Gerrit, Hostomsky Zdenek, Vanarsdale Todd

机构信息

Oncology Research Unit, Pfizer, Inc., 10777 Science Center Drive, San Diego, CA, 92121, USA,

出版信息

Front Med. 2013 Dec;7(4):462-76. doi: 10.1007/s11684-013-0270-6. Epub 2013 Jul 2.

Abstract

Evaluating the effects of novel drugs on appropriate tumor models has become crucial for developing more effective therapies that target highly tumorigenic and drug-resistant cancer stem cell (CSC) populations. In this study, we demonstrate that a subset of cancer cells with CSC properties may be enriched into tumor spheroids under stem cell conditions from a non-small cell lung cancer cell line. Treating these CSC-like cells with gemcitabine alone and a combination of gemcitabine and the novel CHK1 inhibitor PF-00477736 revealed that PF-00477736 enhances the anti-proliferative effect of gemcitabine against both the parental and the CSC-like cell populations. However, the CSC-like cells exhibited resistance to gemcitabine-induced apoptosis. Collectively, the spheroid-forming CSC-like cells may serve as a model system for understanding the mechanism underlying the drug resistance of CSCs and for guiding the development of better therapies that can inhibit tumor growth and eradicate CSCs.

摘要

评估新型药物对合适肿瘤模型的作用,对于开发针对高致瘤性和耐药性癌症干细胞(CSC)群体的更有效疗法而言已变得至关重要。在本研究中,我们证明具有CSC特性的一部分癌细胞在干细胞条件下可从非小细胞肺癌细胞系富集到肿瘤球中。单独用吉西他滨以及用吉西他滨与新型CHK1抑制剂PF - 00477736联合处理这些CSC样细胞,结果显示PF - 00477736增强了吉西他滨对亲本细胞群体和CSC样细胞群体的抗增殖作用。然而,CSC样细胞对吉西他滨诱导的凋亡表现出抗性。总体而言,形成球状体的CSC样细胞可作为一个模型系统,用于理解CSC耐药性的潜在机制,并指导开发能够抑制肿瘤生长和根除CSC的更好疗法。

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