黑色素瘤中硬脂酰-CoA 去饱和酶的诱导可产生细胞密度依赖性铁中毒抵抗。

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of cellular biochemistry Pub Date : 2024-02-16 DOI:10.1002/jcb.30542
Hitomi Shirahama, Yuri Tani, Satomi Tsukahara, Yuka Okamoto, Akiko Hasebe, Tomomiki Noda, Shuji Ando, Masaru Ushijima, Masaaki Matsuura, Akihiro Tomida
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引用次数: 0

摘要

铁氧化是一种调节性细胞死亡,通过抑制消除脂质过氧化的谷胱甘肽过氧化物酶 4(GPX4)来诱导细胞死亡。铁变态反应的诱导受细胞环境的影响。然而,改变铁中毒易感性的细胞状态在很大程度上仍然未知。我们发现,黑色素瘤细胞系会随着细胞密度的增加而对铁中毒产生抗性。转录组和代谢组的比较分析表明,细胞密度依赖性铁中毒抗性与向脂肪生成表型的转变有关,同时伴随着硬脂酰-CoA 去饱和酶(SCD)的强烈诱导。对数百种癌细胞系进行的基因依赖性数据库分析发现,GPX4 和 SCD 依赖性之间存在负相关。重要的是,通过药理或基因敲除抑制 SCD 可使黑色素瘤细胞对 GPX4 抑制敏感,从而减轻高密度细胞的铁中毒抗性。我们的研究结果表明,过渡到SCD诱导的生脂细胞状态会产生依赖于密度的抗铁蛋白沉积能力,这可能会为黑色素瘤提供一种治疗策略。
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Induction of stearoyl-CoA desaturase confers cell density-dependent ferroptosis resistance in melanoma

Ferroptosis is a form of regulated cell death that is induced by inhibiting glutathione peroxidase 4 (GPX4), which eliminates lipid peroxidation. Ferroptosis induction is influenced by the cell environment. However, the cellular states altering ferroptosis susceptibility remain largely unknown. We found that melanoma cell lines became resistant to ferroptosis as cell density increased. Comparative transcriptome and metabolome analyses revealed that cell density-dependent ferroptosis resistance was coupled with a shift toward a lipogenic phenotype accompanied by strong induction of stearoyl-CoA desaturase (SCD). Database analysis of gene dependency across hundreds of cancer cell lines uncovered a negative correlation between GPX4 and SCD dependency. Importantly, SCD inhibition, either pharmacologically or through genetic knockout, sensitized melanoma cells to GPX4 inhibition, thereby attenuating ferroptosis resistance in cells at high density. Our findings indicate that transition to an SCD-inducing, lipogenic cell state produces density-dependent resistance to ferroptosis, which may provide a therapeutic strategy against melanoma.

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来源期刊
Journal of cellular biochemistry
Journal of cellular biochemistry 生物-生化与分子生物学
CiteScore
9.90
自引率
0.00%
发文量
164
审稿时长
1 months
期刊介绍: The Journal of Cellular Biochemistry publishes descriptions of original research in which complex cellular, pathogenic, clinical, or animal model systems are studied by biochemical, molecular, genetic, epigenetic or quantitative ultrastructural approaches. Submission of papers reporting genomic, proteomic, bioinformatics and systems biology approaches to identify and characterize parameters of biological control in a cellular context are encouraged. The areas covered include, but are not restricted to, conditions, agents, regulatory networks, or differentiation states that influence structure, cell cycle & growth control, structure-function relationships.
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