Suppr超能文献

包括明胶酶抑制剂和细胞毒性药物的联合疗法可减少小鼠Lewis肺癌的局部侵袭和转移。

Combination therapy including a gelatinase inhibitor and cytotoxic agent reduces local invasion and metastasis of murine Lewis lung carcinoma.

作者信息

Anderson I C, Shipp M A, Docherty A J, Teicher B A

机构信息

Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

出版信息

Cancer Res. 1996 Feb 15;56(4):715-8.

PMID:8631001
Abstract

The efficacy of combination therapy including an oral gelatinase inhibitor (CT1746) and cytotoxic agent was analyzed using the murine Lewis lung carcinoma model. Primary tumors, pulmonary metastases, and sera from tumor-bearing animals had increased gelatinase B activity that was inhibited by CT1746 levels achievable in vivo. The combination of CT1746 and cyclophosphamide (CTX) was significantly more effective than either single agent in delaying local tumor growth (CT1746/CTX, 30.9 +/- 1.7 days; CT1746, 2.6 +/- 0.3 days; CTX, 19.5 +/- 1.1 days; P < .001) and reducing the number and size of pulmonary metastases [CT1746/CTX, 5 +/- 2 (15% metastases > 3 mm); CT1746, 15 +/- 4 (55% > 3 mm); CTX, 11 +/- 3 (63% > 3 mm); no treatment, 24 +/- 5 (62% > 3 mm); P < .001]. These data support the notion of combining matrix metalloproteinase inhibitors and cytotoxic agents to treat certain epithelial malignancies.

摘要

使用小鼠Lewis肺癌模型分析了包括口服明胶酶抑制剂(CT1746)和细胞毒性药物在内的联合治疗的疗效。原发性肿瘤、肺转移灶以及荷瘤动物的血清中明胶酶B活性升高,而体内可达到的CT1746水平可抑制该活性。CT1746与环磷酰胺(CTX)联合使用在延迟局部肿瘤生长方面(CT1746/CTX,30.9±1.7天;CT1746,2.6±0.3天;CTX,19.5±1.1天;P<.001)以及减少肺转移灶的数量和大小方面(CT1746/CTX,5±2(15%转移灶>3mm);CT1746,15±4(55%>3mm);CTX,11±3(63%>3mm);未治疗,24±5(62%>3mm);P<.001)均明显比单一药物更有效。这些数据支持将基质金属蛋白酶抑制剂和细胞毒性药物联合用于治疗某些上皮性恶性肿瘤的观点。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验