加拿大冷等离子体转化系统治疗:乳腺癌分子亚型细胞活力的有效抑制剂

Q1 Medicine Clinical Plasma Medicine Pub Date : 2020-09-01 DOI:10.1016/j.cpme.2020.100109
Lawan Ly , Xiaoqian Cheng , Saravana R K Murthy , Taisen Zhuang (Supervision) , Olivia Z Jones (Writing – review and editing) , Giacomo Basadonna (Supervision) , Michael Keidar (Supervision) , Jerome Canady (Conceptualization; Funding acquisition; Methodology; Supervision; Writing – review and editing)
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引用次数: 9

摘要

乳腺癌是一种异质性疾病,可根据是否存在雌激素受体(ER)、孕激素受体(PR)和人表皮生长因子2受体(HER2)来划分亚型。冷大气等离子体(CAP)已被证明是一种潜在的癌症治疗方法。在本报告中,CAP治疗使所有7个测试的乳腺癌细胞系的生存能力降低了92-99% (p≤0.05)。增加治疗时间和治疗功率可显著降低乳腺癌细胞活力(** f(2,2)≤0.0176,** f(5,14)≤0.0033)。作者首次报道了乳腺癌对CAP的敏感性是基于受体状态的。受体状态相同的细胞CAP敏感性差异最小(p≤0.05),两种ER+/PR+/HER2-细胞系之间差异为33% (p≤0.05),三种TNBC细胞系之间差异为22-44% (p≤0.05)。her2阴性细胞株,无论ER/PR状态如何,CAP敏感性差异均≤50% (p≤0.05)。此外,ER-/PR-/HER2+ CAP敏感性和ER+/PR+/HER2+ CAP抗性表明,ER/PR状态是决定HER2阳性细胞中CAP敏感性的重要因素。我们关于CAP敏感性的新发现将为如何优化CAP治疗提供见解,以更好地克服CAP耐药性,从而防止肿瘤复发。
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Canady cold plasma conversion system treatment: An effective inhibitor of cell viability in breast cancer molecular subtypes

Breast cancer is a heterogenous disease which can be classified into subtypes by the presence or absence of estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor 2 receptor (HER2). Cold atmospheric plasma (CAP) has been shown to be a potential treatment for cancer. In this report, a 92–99% reduction of viability by CAP treatment was achieved across all seven tested breast cancer cell lines (p ≤ 0.05). Increasing treatment duration and power significantly reduced breast cancer cell viability (** f(2,2) ≤ 0.0176, *** f(5,14) ≤ 0.0033). The authors are the first to report that breast cancer sensitivity to CAP is based on receptor status. Cells with identical receptor status showed the least difference in CAP sensitivity (p ≤ 0.05), the difference being 33% between the two ER+/PR+/HER2- cell lines (p ≤ 0.05) and 22–44% between the three TNBC cell lines (p ≤ 0.05). HER2-negative cell lines, irrespective of ER/PR status, also showed ≤ 50% difference in CAP sensitivity (p ≤ 0.05). Moreover, demonstration of ER-/PR-/HER2+ CAP susceptibility and ER+/PR+/HER2+ CAP resistance suggests that ER/PR status is a significant factor in determining CAP sensitivity in HER2-positive cells. Our novel findings on CAP sensitivity will provide insight on how to optimize CAP treatment to better overcome CAP resistance and thus prevent tumor recurrence.

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Clinical Plasma Medicine
Clinical Plasma Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
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