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ω-6 多不饱和脂肪酸增强实验性肺癌模型中的肿瘤侵袭性:氧化脂类的重要作用。

Omega-6 Polyunsaturated Fatty Acids Enhance Tumor Aggressiveness in Experimental Lung Cancer Model: Important Role of Oxylipins.

机构信息

Programa de Doctorado en Ciencias Biomédicas, Facultad de Medicina, Universidad Nacional Autonoma de Mexico (UNAM), Mexico City 04510, Mexico.

Unidad de Investigacion en Enfermedades Oncologicas, Hospital Infantil de Mexico, Federico Gomez, Mexico City 06720, Mexico.

出版信息

Int J Mol Sci. 2022 May 31;23(11):6179. doi: 10.3390/ijms23116179.

DOI:10.3390/ijms23116179
PMID:35682855
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9181584/
Abstract

Lung cancer is currently the leading cause of cancer death worldwide; it is often diagnosed at an advanced stage and bears poor prognosis. It has been shown that diet is an important environmental factor that contributes to the risk and mortality of several types of cancers. Intake of ω-3 and ω-6 PUFAs plays an important role in cancer risk and progression. Current Western populations have high consumption of ω-6 PUFAs with a ratio of ω-6/ω-3 PUFAs at 15:1 to 16.7:1 This high consumption of ω-6 PUFAs is related to increased cancer risk and progression. However, whether a diet rich in ω-6 PUFAs can contribute to tumor aggressiveness has not been well investigated. We used a murine model of pulmonary squamous cell carcinoma to study the aggressiveness of tumors in mice fed with a diet rich in ω-6 PUFAs and its relationship with oxylipins. Our results shown that the mice fed a diet rich in ω-6 showed a marked increase in proliferation, angiogenesis and pro-inflammatory markers and decreased expression of pro-apoptotic proteins in their tumors. Oxylipin profiling revealed an upregulation of various pro-tumoral oxylipins including PGs, HETEs, DiHETrEs and HODEs. These results demonstrate for the first time that high intake of ω-6 PUFAs in the diet enhances the malignancy of tumor cells by histological changes on tumor dedifferentiation and increases cell proliferation, angiogenesis, pro-inflammatory oxylipins and molecular aggressiveness targets such as NF-κB p65, YY1, COX-2 and TGF-β.

摘要

肺癌是目前全球癌症死亡的主要原因;它通常在晚期被诊断出来,预后不良。已经表明,饮食是导致多种癌症风险和死亡率的重要环境因素。ω-3 和 ω-6 PUFAs 的摄入对癌症风险和进展起着重要作用。目前西方人群 ω-6 PUFAs 的摄入量很高,ω-6/ω-3 PUFAs 的比例为 15:1 到 16.7:1。这种 ω-6 PUFAs 的高摄入量与癌症风险和进展增加有关。然而,富含 ω-6 PUFAs 的饮食是否会导致肿瘤侵袭性增加尚未得到充分研究。我们使用肺鳞癌的小鼠模型来研究富含 ω-6 PUFAs 的饮食对小鼠肿瘤侵袭性的影响及其与氧化脂类的关系。我们的结果表明,喂食富含 ω-6 PUFAs 的饮食的小鼠其肿瘤的增殖、血管生成和促炎标志物明显增加,促凋亡蛋白的表达减少。氧化脂类谱分析显示各种促肿瘤氧化脂类的表达上调,包括 PGs、HETEs、DiHETrEs 和 HODEs。这些结果首次表明,饮食中 ω-6 PUFAs 的高摄入量通过肿瘤去分化的组织学变化增强肿瘤细胞的恶性程度,并增加细胞增殖、血管生成、促炎氧化脂类和 NF-κB p65、YY1、COX-2 和 TGF-β 等分子侵袭性靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f5f/9181584/463a967b1178/ijms-23-06179-g007.jpg
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