利用人体胃癌 AGS 细胞系和腹腔模型在体外模型中进行高热加压腹腔内气溶胶化疗的疗效。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Sa-Hong Min, Jieun Lee, Mira Yoo, Duyeong Hwang, Eunju Lee, So Hyun Kang, Kanghaeng Lee, Young Suk Park, Sang-Hoon Ahn, Yun-Suhk Suh, Do Joong Park, Hyung-Ho Kim
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引用次数: 0

摘要

目的:腹膜癌(PC)是治疗晚期实体瘤的一大挑战,传统疗法因药物渗透性差而受到限制。我们利用人体腹腔模型评估了新型热加压腹腔内气溶胶化疗(HPIPAC)系统对 AGS 胃癌细胞的疗效:材料和方法:使用模拟人体腹腔的模型和 AGS 胃癌细胞系培养皿来评估 HPIPAC 系统的疗效。测量了细胞存活率,以评估 HPIPAC 在 6 种不同条件下的影响:单独加热、PIPAC 与紫杉醇(PTX)、单独 PTX、单独生理盐水(NS)、加热与 NS 以及 HPIPAC 与 PTX:结果表明,HPIPAC 与 PTX 合用时细胞存活率明显降低,表明细胞毒性作用增强。处理后,细胞的平均存活率为 66.6%,48 小时后降至 49.2%,120 小时后再降至 19.6%,这表明处理具有持续的疗效。相比之下,对照组的细胞存活率有所恢复;单独加热组的细胞存活率从 90.8% 上升到 94.4%,PIPAC 和 PTX 组从 82.7% 上升到 89.7%,仅 PTX 组从 73.3% 上升到 74.8%,仅 NS 组从 90.9% 上升到 98.3%,加热和 NS 组从 74.4% 上升到 84.7%:带有 PTX 的 HPIPAC 系统是一种治疗胃癌 PC 的有效方法,可显著降低细胞活力。尽管存在一些局限性,但本研究强调了该系统在提高治疗效果方面的潜力。今后的工作重点应是完善 HPIPAC 并验证其在临床环境中的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of Hyperthermic Pressurized Intraperitoneal Aerosol Chemotherapy in an In Vitro Model Using a Human Gastric Cancer AGS Cell Line and an Abdominal Cavity Model.

Purpose: Peritoneal carcinomatosis (PC) presents a major challenge in the treatment of late-stage, solid tumors, with traditional therapies limited by poor drug penetration. We evaluated a novel hyperthermic pressurized intraperitoneal aerosol chemotherapy (HPIPAC) system using a human abdominal cavity model for its efficacy against AGS gastric cancer cells.

Materials and methods: A model simulating the human abdominal cavity and AGS gastric cancer cell line cultured dishes were used to assess the efficacy of the HPIPAC system. Cell viability was measured to evaluate the impact of HPIPAC under 6 different conditions: heat alone, PIPAC with paclitaxel (PTX), PTX alone, normal saline (NS) alone, heat with NS, and HPIPAC with PTX.

Results: Results showed a significant reduction in cell viability with HPIPAC combined with PTX, indicating enhanced cytotoxic effects. Immediately after treatment, the average cell viability was 66.6%, which decreased to 49.2% after 48 hours and to a further 19.6% after 120 hours of incubation, demonstrating the sustained efficacy of the treatment. In contrast, control groups exhibited a recovery in cell viability; heat alone showed cell viability increasing from 90.8% to 94.4%, PIPAC with PTX from 82.7% to 89.7%, PTX only from 73.3% to 74.8%, NS only from 90.9% to 98.3%, and heat with NS from 74.4% to 84.7%.

Conclusions: The HPIPAC system with PTX exhibits a promising approach in the treatment of PC in gastric cancer, significantly reducing cell viability. Despite certain limitations, this study highlights the system's potential to enhance treatment outcomes. Future efforts should focus on refining HPIPAC and validating its effectiveness in clinical settings.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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