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一种新型胞嘧啶类似物 RX-3117,在异种移植模型中显示出强大的疗效,甚至对吉西他滨耐药的肿瘤也是如此。

A novel cytidine analog, RX-3117, shows potent efficacy in xenograft models, even in tumors that are resistant to gemcitabine.

机构信息

Rexahn Pharmaceuticals, Rockville, MD, U.S.A.

Teva Pharmaceuticals Industries LTD., Petach Tikva, Israel.

出版信息

Anticancer Res. 2014 Dec;34(12):6951-9.

Abstract

RX-3117 (fluorocyclopentenylcytosine) is a cytidine analog and this class of drugs, including gemcitabine, has been widely used for the treatment of various types of cancers. However, there is no oral formulation of gemcitabine and drug resistance to gemcitabine is common. In this study, the efficacy of orally-administered RX-3117 was examined in 9 different human tumor xenograft models (colon, non-small cell lung, small cell lung, pancreatic, renal and cervical), grown subcutaneously in athymic nude mice. In the Colo 205, H460, H69 and CaSki models, gemcitabine treatment resulted in 28%, 30%, 25% and 0% tumor growth inhibition (TGI), respectively, whereas oral treatment with RX-3117 induced 100%, 78%, 62% and 66% TGI, respectively. This indicates that RX-3117 may have the potential to be used for the treatment of tumors that do not respond to gemcitabine. RX-3117 was also evaluated in a single primary low-passage human pancreatic Tumorgraft™CTG-0298 (TGI 76%), which is relatively resistant to gemcitabine (TGI 38%) and has a favorable RX-3117-activating enzyme profile. These studies demonstrated the therapeutic potential and anticancer efficacy of RX-3117.

摘要

RX-3117(氟环胞苷)是一种胞苷类似物,这类药物包括吉西他滨,已广泛用于治疗各种类型的癌症。然而,吉西他滨没有口服制剂,而且对吉西他滨的耐药性很常见。在这项研究中,研究人员在 9 种不同的人肿瘤异种移植模型(结肠、非小细胞肺癌、小细胞肺癌、胰腺、肾和宫颈)中,检查了口服 RX-3117 的疗效,这些肿瘤在无胸腺裸鼠皮下生长。在 Colo 205、H460、H69 和 CaSki 模型中,吉西他滨治疗导致肿瘤生长抑制(TGI)分别为 28%、30%、25%和 0%,而口服 RX-3117 治疗分别诱导 100%、78%、62%和 66%的 TGI。这表明 RX-3117 可能有潜力用于治疗对吉西他滨无反应的肿瘤。RX-3117 还在一个单一的原发低传代人胰腺 Tumorgraft™CTG-0298(TGI 为 76%)中进行了评估,该肿瘤对吉西他滨相对耐药(TGI 为 38%),并且具有有利的 RX-3117 激活酶谱。这些研究证明了 RX-3117 的治疗潜力和抗癌疗效。

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