Elucidating the Mechanisms of Acquired Palbociclib Resistance via Comprehensive Metabolomics Profiling.

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Current Issues in Molecular Biology Pub Date : 2025-01-02 DOI:10.3390/cimb47010024
Lulu Yang, Yajun Yue, Zhendong Wang, You Jiang, Zhichao Xue, Yongzhuo Zhang
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Abstract

Palbociclib is a cyclin-dependent kinase 4/6 inhibitor and a commonly used antitumor drug. Many cancers are susceptible to palbociclib resistance, however, the underlying metabolism mechanism and extent of resistance to palbociclib are unknown. In this study, LC-MS metabolomics was used to investigate the metabolite changes of colorectal cancer SW620 cells that were resistant to palbociclib. The study indicated that there were 76 metabolite expression differences between SW620 cells with palbociclib resistance and the parental SW620 cells involving amino acids, glutathione, ABC transporters, and so on. MetaboAnalyst 6.0 metabolic pathway analysis showed that arginine synthesis, β-alanine metabolism, and purine metabolism were disrupted. These results may provide potential clues to the metabolism mechanism of drug resistance in cancer cells that are resistant to palbociclib. Our study has the potential to contribute to the study of anti-palbociclib resistance.

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通过综合代谢组学分析阐明获得性帕博西尼耐药机制。
帕博西尼是一种周期蛋白依赖性激酶4/6抑制剂,是一种常用的抗肿瘤药物。许多癌症易发生帕博西尼耐药,然而,对帕博西尼的潜在代谢机制和耐药程度尚不清楚。本研究采用LC-MS代谢组学方法研究耐药palbociclib的结直肠癌SW620细胞的代谢物变化。研究表明,帕博西尼耐药SW620细胞与亲本SW620细胞之间存在76种代谢物表达差异,涉及氨基酸、谷胱甘肽、ABC转运蛋白等。代谢途径分析显示,精氨酸合成、β-丙氨酸代谢和嘌呤代谢被破坏。这些结果可能为帕博西尼耐药的癌细胞耐药代谢机制提供潜在线索。我们的研究有可能为抗帕博西尼耐药的研究做出贡献。
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来源期刊
Current Issues in Molecular Biology
Current Issues in Molecular Biology 生物-生化研究方法
CiteScore
2.90
自引率
3.20%
发文量
380
审稿时长
>12 weeks
期刊介绍: Current Issues in Molecular Biology (CIMB) is a peer-reviewed journal publishing review articles and minireviews in all areas of molecular biology and microbiology. Submitted articles are subject to an Article Processing Charge (APC) and are open access immediately upon publication. All manuscripts undergo a peer-review process.
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