Quantitative Phosphoproteomics and Acetylomics of Safranal Anticancer Effects in Triple-Negative Breast Cancer Cells

被引:7
作者
Ashrafian, Shahrbanou [1 ]
Zarrineh, Mahshid [1 ,3 ]
Jensen, Pia [2 ]
Nawrocki, Arkadiusz [2 ]
Rezadoost, Hassan [1 ]
Ansari, Alireza Madjid [4 ]
Farahmand, Leila [4 ]
Ghassempour, Alireza [1 ]
Larsen, Martin R. [2 ]
机构
[1] Shahid Beheshti Univ, Med Plants & Drugs Res Inst, Tehran 1983963113, Iran
[2] Univ Southern Denmark, Dept Biochem & Mol Biol, Prot Res Grp, DK-5230 Odense, Denmark
[3] Karolinska Inst, Dept Oncol & Pathol, Sci Life Lab, SE-17165 Solna, Sweden
[4] ACECR, Moatamed Canc Inst, Breast Canc Res Ctr, Integrat Oncol Dept, Tehran 1517964311, Iran
关键词
triple-negative breast cancer; TMT labeling; phosphoproteomoics; acetylomics; GROWTH-FACTOR RECEPTOR; REPLICATION PROTEIN-A; HISTONE DEACETYLASE INHIBITORS; DNA-REPLICATION; PHOSPHORYLATION SITES; C-JUN; TRANSLATION INITIATION; CYCLE; APOPTOSIS; IDENTIFICATION;
D O I
10.1021/acs.jproteome.2c00168
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Safranal, as an aroma in saffron, is one of the cytotoxic compounds in saffron that causes cell death in triple negative breast cancer cells. Our recent research reported the anticancer effects of safranal, which further demonstrated its impact on protein translation, mitochondrial dysfunction, and DNA fragmentation. To better understand the underlying mechanisms, we identified acetylated and phosphorylated peptides in safranaltreated cancer cells. We conducted a comprehensive phosphoproteomics and acetylomics analysis of safranal-treated MDA-MB-231 cells by using a combination of TMT labeling and enrichment methods including titanium dioxide and immunoprecipitation. We provide a wide range of phosphoproteome regulation in different signaling pathways that are disrupted by safranal treatment. Safranal influences the phosphorylation level on proteins involved in DNA replication and repair, translation, and EGFR activation/ accumulation, which can lead the cells into apoptosis. Safranal causes DNA damage which is followed by the activation of cell cycle checkpoints for DNA repair. Over time, checkpoints and DNA repair are inhibited and cells are under a mitotic catastrophe. Moreover, safranal prevents repair by the hypo-acetylation of H4 and facilitates the transcription of proapoptotic genes by hyperacetylation of H3, which push the cells to the brink of death.
引用
收藏
页码:2566 / 2585
页数:20
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