Methoxychalcones as potential anticancer agents for colon cancer: Is membrane perturbing potency relevant?

IF 2.8 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et biophysica acta. General subjects Pub Date : 2024-02-08 DOI:10.1016/j.bbagen.2024.130581
Anna Palko-Łabuz , Olga Wesołowska , Maria Błaszczyk , Anna Uryga , Beata Sobieszczańska , Magdalena Skonieczna , Edyta Kostrzewa-Susłow , Tomasz Janeczko , Kamila Środa-Pomianek
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Abstract

Chalcones are naturally produced by many plants, and constitute precursors for the synthesis of flavons and flavanons. They were shown to possess antibacterial, antifungal, anti-cancer, and anti- inflammatory properties. The goal of the study was to assess the suitability of three synthetic methoxychalcones as potential anticancer agents. In a panel of colon cancer cell lines they were demonstrated to be cytotoxic, proapoptotic, causing cell cycle arrest, and increasing intracellular level of reactive oxygen species. Anticancer activity of the compounds was not diminished in the presence of stool extract containing microbial enzymes that could change the structure of chalcones. Moreover, methoxychalcones interacted strongly with model phosphatidylcholine membranes as detected by differential scanning calorimetry. Metohoxychalcones particularly affected the properties of lipid domains in giant unilamellar liposomes formed from raft-mimicking lipid composition. This may be of importance since many molecular targets for therapy of metastatic colon cancer are raft-associated receptors (e.g., receptor tyrosine kinases). The importance of membrane perturbing potency of methoxychalcones for their biological activity was additionally corroborated by the results obtained by molecular modelling.

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甲氧基查耳酮作为潜在的结肠癌抗癌剂:膜扰动效力是否相关?
查尔酮是由许多植物天然生成的,是合成黄酮和黄烷酮的前体。研究表明,它们具有抗菌、抗真菌、抗癌和抗炎特性。这项研究的目的是评估三种合成甲氧基查尔酮作为潜在抗癌剂的适用性。在一组结肠癌细胞系中,这些化合物被证明具有细胞毒性、促凋亡、导致细胞周期停滞和增加细胞内活性氧水平。在含有微生物酶的粪便提取物存在的情况下,这些化合物的抗癌活性并没有降低,因为微生物酶可以改变查耳酮的结构。此外,通过差示扫描量热法检测到,甲氧基查耳酮与模型磷脂酰胆碱膜有强烈的相互作用。甲氧基查耳酮尤其会影响由模拟筏状脂质组成的巨型单层脂质体中脂质结构域的特性。这一点可能很重要,因为治疗转移性结肠癌的许多分子靶点都是筏相关受体(如受体酪氨酸激酶)。分子建模的结果也证实了甲氧基查耳酮的膜扰动效力对其生物活性的重要性。
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来源期刊
Biochimica et biophysica acta. General subjects
Biochimica et biophysica acta. General subjects 生物-生化与分子生物学
CiteScore
6.40
自引率
0.00%
发文量
139
审稿时长
30 days
期刊介绍: BBA General Subjects accepts for submission either original, hypothesis-driven studies or reviews covering subjects in biochemistry and biophysics that are considered to have general interest for a wide audience. Manuscripts with interdisciplinary approaches are especially encouraged.
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