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硬脂酰辅酶 A 去饱和酶 1 作为一种治疗性生物标志物:聚焦于癌症干细胞。

Stearoyl-CoA Desaturase 1 as a Therapeutic Biomarker: Focusing on Cancer Stem Cells.

机构信息

Department of Chemistry, College of Convergence and Integrated Science, Kyonggi University, Suwon 16227, Gyeonggi-do, Republic of Korea.

出版信息

Int J Mol Sci. 2023 May 18;24(10):8951. doi: 10.3390/ijms24108951.

Abstract

The dysregulation of lipid metabolism and alterations in the ratio of monounsaturated fatty acids (MUFAs) to saturated fatty acids (SFAs) have been implicated in cancer progression and stemness. Stearoyl-CoA desaturase 1 (SCD1), an enzyme involved in lipid desaturation, is crucial in regulating this ratio and has been identified as an important regulator of cancer cell survival and progression. SCD1 converts SFAs into MUFAs and is important for maintaining membrane fluidity, cellular signaling, and gene expression. Many malignancies, including cancer stem cells, have been reported to exhibit high expression of SCD1. Therefore, targeting SCD1 may provide a novel therapeutic strategy for cancer treatment. In addition, the involvement of SCD1 in cancer stem cells has been observed in various types of cancer. Some natural products have the potential to inhibit SCD1 expression/activity, thereby suppressing cancer cell survival and self-renewal activity.

摘要

脂质代谢失调和单不饱和脂肪酸 (MUFAs) 与饱和脂肪酸 (SFAs) 比例的改变与癌症进展和干性有关。参与脂质去饱和的酶酰基辅酶 A 去饱和酶 1 (SCD1) 对于调节这种比例至关重要,并且已被确定为癌细胞存活和进展的重要调节剂。SCD1 将 SFAs 转化为 MUFAs,对于维持膜流动性、细胞信号传导和基因表达非常重要。许多恶性肿瘤,包括癌症干细胞,据报道 SCD1 表达水平较高。因此,靶向 SCD1 可能为癌症治疗提供新的治疗策略。此外,SCD1 参与各种类型癌症的癌症干细胞。一些天然产物具有抑制 SCD1 表达/活性的潜力,从而抑制癌细胞的存活和自我更新活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7bb/10219200/3bfac4200eb3/ijms-24-08951-g001.jpg

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