A stearate-rich diet and oleate restriction directly inhibit tumor growth via the unfolded protein response

IF 9.5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Experimental and Molecular Medicine Pub Date : 2024-12-02 DOI:10.1038/s12276-024-01356-2
Jumpei Ogura, Koji Yamanoi, Kentaro Ishida, Eijiro Nakamura, Shinji Ito, Naoki Aoyama, Yuki Nakanishi, Toshi Menju, Kosuke Kawaguchi, Yuko Hosoe, Mana Taki, Ryusuke Murakami, Ken Yamaguchi, Junzo Hamanishi, Masaki Mandai
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Abstract

Fatty acids are known to have significant effects on the properties of cancer cells. Therefore, these compounds have been incorporated into therapeutic strategies. However, few studies have examined the effects of individual fatty acids and their interactions in depth. This study analyzed the effects of various fatty acids on cancer cells and revealed that stearic acid, an abundant saturated fatty acid, had a stronger inhibitory effect on cell growth than did palmitic acid, which is also an abundant saturated fatty acid, by inducing DNA damage and apoptosis through the unfolded protein response (UPR) pathway. Intriguingly, the negative effects of stearate were reduced by the presence of oleate, a different type of abundant fatty acid. We combined a stearate-rich diet with the inhibition of stearoyl-CoA desaturase-1 to explore the impact of diet on tumor growth. This intervention significantly reduced tumor growth in both ovarian cancer models and patient-derived xenografts (PDXs), including those with chemotherapy resistance, notably by increasing stearate levels while reducing oleate levels within the tumors. Conversely, the negative effects of a stearate-rich diet were mitigated by an oleate-rich diet. This study revealed that dietary stearate can directly inhibit tumor growth through mechanisms involving DNA damage and apoptosis mediated by the UPR pathway. These results suggest that dietary interventions, which increase stearic acid levels while decreasing oleic acid levels, may be promising therapeutic strategies for cancer treatment. These results could lead to the development of new cancer treatment strategies. Obesity, characterized by excessive body fat, is linked to higher cancer risks. Researchers explored how specific fatty acids impact cancer growth. The study focused on palmitate, stearate, and oleate, using various cancer cell lines and patient derived xenograft. They found that stearate significantly inhibited cancer cell growth more than palmitate. This was a controlled experiment involving human cancer cell lines and mice fed specialized diets. Results showed that stearate induced DNA damage and cancer cell death, while oleate reduced these effects. The researchers concluded that dietary stearate could suppress tumor growth, especially when combined with inhibitors of fatty acid conversion. Future research could explore dietary interventions as potential cancer treatments. This summary was initially drafted using artificial intelligence, then revised and fact-checked by the author.

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富含硬脂酸的饮食和油酸限制通过未折叠蛋白反应直接抑制肿瘤生长。
众所周知,脂肪酸对癌细胞的特性有显著的影响。因此,这些化合物已被纳入治疗策略。然而,很少有研究深入研究单个脂肪酸的影响及其相互作用。本研究分析了各种脂肪酸对癌细胞的影响,发现硬脂酸作为一种丰富的饱和脂肪酸,其对癌细胞生长的抑制作用强于棕榈酸,棕榈酸也是一种丰富的饱和脂肪酸,它通过未折叠蛋白反应(UPR)途径诱导DNA损伤和细胞凋亡。有趣的是,硬脂酸的负面影响被油酸(一种不同类型的丰富脂肪酸)的存在所减少。我们将富含硬脂酸的饮食与抑制硬脂酰辅酶a去饱和酶-1相结合,以探索饮食对肿瘤生长的影响。这种干预显著降低了卵巢癌模型和患者来源的异种移植物(PDXs)的肿瘤生长,包括那些化疗耐药的肿瘤,特别是通过增加硬脂酸水平而降低肿瘤内的油酸水平。相反,富含硬脂酸的饮食的负面影响被富含油酸的饮食所减轻。本研究表明,膳食硬脂酸盐可通过UPR通路介导的DNA损伤和细胞凋亡等机制直接抑制肿瘤生长。这些结果表明,增加硬脂酸水平而降低油酸水平的饮食干预可能是治疗癌症的有希望的治疗策略。这些结果可能会导致新的癌症治疗策略的发展。
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来源期刊
Experimental and Molecular Medicine
Experimental and Molecular Medicine 医学-生化与分子生物学
CiteScore
19.50
自引率
0.80%
发文量
166
审稿时长
3 months
期刊介绍: Experimental & Molecular Medicine (EMM) stands as Korea's pioneering biochemistry journal, established in 1964 and rejuvenated in 1996 as an Open Access, fully peer-reviewed international journal. Dedicated to advancing translational research and showcasing recent breakthroughs in the biomedical realm, EMM invites submissions encompassing genetic, molecular, and cellular studies of human physiology and diseases. Emphasizing the correlation between experimental and translational research and enhanced clinical benefits, the journal actively encourages contributions employing specific molecular tools. Welcoming studies that bridge basic discoveries with clinical relevance, alongside articles demonstrating clear in vivo significance and novelty, Experimental & Molecular Medicine proudly serves as an open-access, online-only repository of cutting-edge medical research.
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