化疗
医学
肿瘤科
癌症
免疫疗法
顺铂
可药性
伊立替康
内科学
小分子
恶性肿瘤
肺癌
转移
癌症研究
合成致死
靶向治疗
小细胞肺癌
细胞
前药
联合化疗
小细胞癌
肿瘤
治疗指标
治疗效果
生长抑制
癌细胞
细胞生长
作者
Alvaro Quintanal-Villalonga,Hirokazu Taniguchi,Yuan Hao,Andrew Chow,Yingqian A. Zhan,Shweta S. Chavan,Fathema Uddin,Viola Allaj,Parvathy Manoj,Nisargbhai S. Shah,Joseph M. Chan,Michael Offin,Metamia Ciampricotti,Jordana Ray-Kirton,Jacklynn Egger,Umesh Bhanot,Irina Linkov,Marina Asher,Michael H. Roehrl,Juan Qiu
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2021-11-23
卷期号:82 (3): 472-483
被引量:48
标识
DOI:10.1158/0008-5472.can-21-2964
摘要
knockout enhanced chemosensitivity, and exportin-1 inhibition demonstrated synergy with both first- and second-line chemotherapy. The small molecule exportin-1 inhibitor selinexor in combination with cisplatin or irinotecan dramatically inhibited tumor growth in chemonaïve and chemorelapsed SCLC patient-derived xenografts, respectively. Together these data identify exportin-1 as a promising therapeutic target in SCLC, with the potential to markedly augment the efficacy of cytotoxic agents commonly used in treating this disease. SIGNIFICANCE: CRISPR-Cas9 screening nominates exportin-1 as a therapeutic target in SCLC, and exportin-1 inhibition enhances chemotherapy efficacy in patient-derived xenografts, providing a novel therapeutic opportunity in this disease.
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