首页> 美国卫生研究院文献>Cancers >Sequestration of 9-Hydroxystearic Acid in FAHFA (Fatty Acid Esters of Hydroxy Fatty Acids) as a Protective Mechanism for Colon Carcinoma Cells to Avoid Apoptotic Cell Death
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Sequestration of 9-Hydroxystearic Acid in FAHFA (Fatty Acid Esters of Hydroxy Fatty Acids) as a Protective Mechanism for Colon Carcinoma Cells to Avoid Apoptotic Cell Death

机译:螯合FAHFA(羟基脂肪酸的脂肪酸酯)中的9-羟基硬脂酸作为结肠癌细胞避免凋亡细胞死亡的保护机制

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摘要

Hydroxy fatty acids are known to cause cell cycle arrest and apoptosis. The best studied of them, 9-hydroxystearic acid (9-HSA), induces apoptosis in cell lines by acting through mechanisms involving different targets. Using mass spectrometry-based lipidomic approaches, we show in this study that 9-HSA levels in human colorectal tumors are diminished when compared with normal adjacent tissue. Since this decrease could be compatible with an escape mechanism of tumors from 9-HSA-induced apoptosis, we investigated different features of the utilization of this hydroxyfatty acid in colon. We show that in colorectal tumors and related cell lines such as HT-29 and HCT-116, 9-HSA is the only hydroxyfatty acid constituent of branched fatty acid esters of hydroxyfatty acids (FAHFA), a novel family of lipids with anti-inflammatory properties. Importantly, FAHFA levels in tumors are elevated compared with normal tissue and, unlike 9-HSA, they do not induce apoptosis of colorectal cell lines over a wide range of concentrations. Further, the addition of 9-HSA to colon cancer cell lines augments the synthesis of different FAHFA before the cells commit to apoptosis, suggesting that FAHFA formation may function as a buffer system that sequesters the hydroxyacid into an inactive form, thereby restricting apoptosis.
机译:已知羟基脂肪酸会导致细胞周期停滞和凋亡。其中最深入的研究是9-羟基硬脂酸(9-HSA),它通过涉及不同靶标的机制起作用,诱导细胞系凋亡。使用基于质谱的脂质组学方法,我们在这项研究中显示,与正常的相邻组织相比,人结肠直肠肿瘤中的9-HSA水平降低了。由于这种减少可能与9-HSA诱导的细胞凋亡的肿瘤逃逸机制兼容,因此我们研究了在结肠中利用这种羟基脂肪酸的不同特征。我们显示,在结直肠肿瘤和相关细胞系(例如HT-29和HCT-116)中,9-HSA是羟基脂肪酸(FAHFA)(具有消炎作用的新型脂质家族)的支链脂肪酸酯的唯一羟基脂肪酸成分属性。重要的是,与正常组织相比,肿瘤中的FAHFA水平升高,并且与9-HSA不同,它们在宽范围的浓度下都不会诱导结直肠细胞系凋亡。此外,向结肠癌细胞系中添加9-HSA可以增强不同FAHFA在细胞发生凋亡之前的合成,这表明FAHFA的形成可能是将羟酸螯合成非活性形式的缓冲系统,从而限制了细胞凋亡。

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