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艾西司他丁与多西他赛联合使用可抑制人肺癌的生长和转移,并延长原位肺肿瘤无胸腺裸鼠的生存期。

Exisulind in combination with docetaxel inhibits growth and metastasis of human lung cancer and prolongs survival in athymic nude rats with orthotopic lung tumors.

作者信息

Chan Daniel C, Earle Keith A, Zhao Tom L M, Helfrich Barbara, Zeng Chan, Baron Anna, Whitehead Clark M, Piazza Gary, Pamukcu Rifat, Thompson W Joseph, Alila Hector, Nelson Peter, Bunn Paul A

机构信息

University of Colorado Cancer Center, Department of Medicine, Preventive Medicine and Biostatistics, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA.

出版信息

Clin Cancer Res. 2002 Mar;8(3):904-12.

Abstract

Docetaxel, a semisynthetic taxane, improves the survival of stage IIIB and IV non-small cell lung cancer patients. However, the 5-year survival remains poor, and few patients experience a complete remission. In this report, we evaluated the effects of exisulind, a novel proapoptotic agent that is a sulfone metabolite of sulindac, in combination with docetaxel on the growth of the human non-small cell lung cancer cell line A549 in vitro and in vivo. Exisulind is a novel sulindac metabolite in that it does not inhibit cyclooxygenase enzymes and has been shown to induce apoptosis in a variety of human cancers by inhibiting cyclic GMP-dependent phosphodiesterase. Exisulind alone increased the fraction of cells in the G(1) phase of the cell cycle from 46% to 65%, whereas it decreased the fraction of cells in the S phase from 38% to 14%. Docetaxel increased the fraction of cells in the S phase from 17% to 19%, and 10 nM docetaxel increased the G2-M phase by 23%. Docetaxel alone induced apoptosis from 11% to 64% at 12-24 h after incubation. The combination of exisulind with concentrations of docetaxel (in concentrations that alone did not alter cell cycle distribution) reduced the G(1) accumulation induced by exisulind, increased the fraction of cells in G(2)-M (9-17%), and increased apoptosis (5-62%). The IC(50) for in vitro growth inhibition by exisulind alone was approximately 200 microM and 2.5 nM for docetaxel. The in vitro combination of exisulind and docetaxel produced an additive to synergistic growth inhibition. In athymic nude rats with A549 orthotopic lung cancers, both exisulind and docetaxel alone moderately prolonged survival, inhibited tumor growth and metastases, and increased apoptosis compared with control animals treated with a carrier. However, the combination of exisulind with docetaxel significantly prolonged survival (P = < 0.0004), inhibited tumor growth and metastases (P = < 0.0001), and increased apoptosis (P = < 0.001) when compared with control animals. These results provide rationale for conducting clinical trials using the combination of exisulind and docetaxel in patients with advanced lung cancer.

摘要

多西他赛是一种半合成紫杉烷,可提高IIIB期和IV期非小细胞肺癌患者的生存率。然而,其5年生存率仍然很低,很少有患者能实现完全缓解。在本报告中,我们评估了新型促凋亡药物依西美坦(一种舒林酸的砜代谢产物)与多西他赛联合使用对人非小细胞肺癌细胞系A549体外和体内生长的影响。依西美坦是一种新型舒林酸代谢产物,它不抑制环氧化酶,并且已被证明可通过抑制环鸟苷酸依赖性磷酸二酯酶在多种人类癌症中诱导细胞凋亡。单独使用依西美坦可使细胞周期G(1)期的细胞比例从46%增加到65%,而使S期的细胞比例从38%降至14%。多西他赛使S期的细胞比例从17%增加到19%,10 nM多西他赛使G2-M期增加23%。单独使用多西他赛在孵育12 - 24小时后可使细胞凋亡率从11%诱导至64%。依西美坦与多西他赛浓度联合使用(单独使用时不改变细胞周期分布的浓度)可减少依西美坦诱导的G(1)期积累,增加G(2)-M期的细胞比例(9 - 17%),并增加细胞凋亡率(5 - 62%)。依西美坦单独体外生长抑制的IC(50)约为200 microM,多西他赛为2.5 nM。依西美坦和多西他赛的体外联合产生了相加至协同的生长抑制作用。在患有A549原位肺癌的无胸腺裸鼠中,与用载体处理的对照动物相比,依西美坦和多西他赛单独使用均适度延长了生存期,抑制了肿瘤生长和转移,并增加了细胞凋亡。然而,与对照动物相比,依西美坦与多西他赛联合使用显著延长了生存期(P = < 0.0004),抑制了肿瘤生长和转移(P = < 0.0001),并增加了细胞凋亡(P = < 0.001)。这些结果为在晚期肺癌患者中使用依西美坦和多西他赛联合进行临床试验提供了理论依据。

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