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不饱和脂肪酸对新鲜人体肿瘤外植体的细胞毒性:浓度阈值及其对临床疗效的影响。

Cytotoxicity of unsaturated fatty acids in fresh human tumor explants: concentration thresholds and implications for clinical efficacy.

出版信息

Lipids Health Dis. 2009 Dec 15;8:54. doi: 10.1186/1476-511X-8-54.

Abstract

BACKGROUND

Unsaturated fatty acids (UFAs) exhibit in vitro cytotoxicity against many malignant cell lines and yield decreased cancer incidence and reduced tumor growth in animal models. But clinical and animal studies to date have achieved response using only localized delivery methods such as intratumoral infusion. To explore possibilities for enhanced clinical efficacy, fresh surgical explants of tumors from 22 patients with five malignancies were exposed to gamma-linolenic acid (GLA) and alpha-linolenic acid (ALA) and analyzed with an in vitro chemosensitivity testing system, the Fluorescent Cytoprint Assay (FCA). A total of 282 micro-organ cultures derived from these malignant tumors were exposed to GLA and ALA at different concentrations.

RESULTS

GLA and ALA exhibited greater than 90% cytotoxicity at a sharp concentration threshold between 500 microM and 1 mM against all but two malignant micro-organ cultures tested in 5-10% serum. In tests using 30-40% serum, GLA and ALA killed tumor at concentrations of 2 mM and above.

CONCLUSIONS

The concentration threshold of 500 microM to 2 mM exhibited for antitumor activity by GLA and ALA is much higher than that observed in most previously reported cell culture studies but consistent with physiological concentrations found to kill tumor clinically and in animals. A mechanism of antitumor activity by unsaturated fatty acids through selective destabilization of the malignant plasma membrane is considered. An oral regimen is proposed for phase I clinical testing that could push the area under the curve for serum concentration of unbound unsaturated fatty acids over time to much higher levels than previously achieved for systemic administration and into the range that could yield antitumor response.

摘要

背景

不饱和脂肪酸(UFAs)在体外对许多恶性细胞系表现出细胞毒性,并在动物模型中降低癌症发病率和肿瘤生长。但迄今为止的临床和动物研究仅使用局部递送方法(如肿瘤内输注)取得了疗效。为了探索提高临床疗效的可能性,对来自 5 种恶性肿瘤的 22 名患者的新鲜手术肿瘤标本进行了 γ-亚麻酸(GLA)和α-亚麻酸(ALA)暴露,并使用体外药敏检测系统,即荧光细胞打印测定(FCA)进行了分析。总共从这些恶性肿瘤中获得了 282 个微组织培养物,并在不同浓度下暴露于 GLA 和 ALA。

结果

GLA 和 ALA 在 5-10%血清中对所有恶性微生物培养物的浓度阈值在 500 microM 至 1 mM 之间,表现出大于 90%的细胞毒性。在使用 30-40%血清的测试中,GLA 和 ALA 在 2 mM 及以上浓度下杀死肿瘤。

结论

GLA 和 ALA 表现出的抗肿瘤活性的浓度阈值为 500 microM 至 2 mM,远高于大多数先前报道的细胞培养研究中观察到的浓度阈值,但与临床上和动物中发现的杀死肿瘤的生理浓度一致。认为不饱和脂肪酸通过选择性破坏恶性质膜发挥抗肿瘤活性的机制。提出了一种用于 I 期临床试验的口服方案,该方案可以随着时间的推移将血清中未结合不饱和脂肪酸的曲线下面积推高到比以前全身给药所达到的水平高得多的水平,并进入可能产生抗肿瘤反应的范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85a1/2801488/d3d5ff1636eb/1476-511X-8-54-1.jpg

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