人血清可抵消表皮生长因子受体/HER2靶向药物拉帕替尼对鳞癌SK-BR-3细胞生长和基因表达的影响

IF 2.3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochemistry (Moscow) Pub Date : 2024-04-08 DOI:10.1134/S000629792403009X
Nina Shaban, Mikhail Raevskiy, Galina Zakharova, Victoria Shipunova, Sergey Deyev, Maria Suntsova, Maksim Sorokin, Anton Buzdin, Dmitri Kamashev
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引用次数: 0

摘要

摘要 拉帕替尼是一种抑制HER2和表皮生长因子受体蛋白的靶向治疗药物。它被用于治疗 HER2 阳性乳腺癌,但并非所有患者都对它有反应。我们利用 14 位女性捐献者的血清样本(单独采集或合并采集)发现,人类血清会显著降低拉帕替尼介导的对人类乳腺鳞癌 SK-BR-3 细胞系生长的抑制作用。拉帕替尼与人血清之间的这种拮抗作用与药物诱导的G1/S细胞周期转换停滞被取消有关。RNA 测序显示,在拉帕替尼存在的情况下,有 308 个基因表达不同。值得注意的是,人血清与拉帕替尼合用时,既能恢复细胞的生长速度,也能恢复96.1%的基因表达,而这些基因的表达在单独使用拉帕替尼治疗时发生了改变。EGF与拉帕替尼联合给药也能恢复细胞生长,并消除95.8%的拉帕替尼治疗SK-BR-3细胞时特有的基因表达改变。差异基因表达分析还显示,在人血清或EGF存在的情况下,拉帕替尼无法抑制Toll-Like受体信号通路,也无法改变与基因本体术语 "病灶粘附 "相关的基因的表达。
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Human Blood Serum Counteracts EGFR/HER2-Targeted Drug Lapatinib Impact on Squamous Carcinoma SK-BR-3 Cell Growth and Gene Expression

Lapatinib is a targeted therapeutic inhibiting HER2 and EGFR proteins. It is used for the therapy of HER2-positive breast cancer, although not all the patients respond to it. Using human blood serum samples from 14 female donors (separately taken or combined), we found that human blood serum dramatically abolishes the lapatinib-mediated inhibition of growth of the human breast squamous carcinoma SK-BR-3 cell line. This antagonism between lapatinib and human serum was associated with cancelation of the drug induced G1/S cell cycle transition arrest. RNA sequencing revealed 308 differentially expressed genes in the presence of lapatinib. Remarkably, when combined with lapatinib, human blood serum showed the capacity of restoring both the rate of cell growth, and the expression of 96.1% of the genes expression of which were altered by the lapatinib treatment alone. Co-administration of EGF with lapatinib also restores the cell growth and cancels alteration of expression of 95.8% of the genes specific to lapatinib treatment of SK-BR-3 cells. Differential gene expression analysis also showed that in the presence of human serum or EGF, lapatinib was unable to inhibit the Toll-Like Receptor signaling pathway and alter expression of genes linked to the Gene Ontology term of Focal adhesion.

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来源期刊
Biochemistry (Moscow)
Biochemistry (Moscow) 生物-生化与分子生物学
CiteScore
4.70
自引率
3.60%
发文量
139
审稿时长
2 months
期刊介绍: Biochemistry (Moscow) is the journal that includes research papers in all fields of biochemistry as well as biochemical aspects of molecular biology, bioorganic chemistry, microbiology, immunology, physiology, and biomedical sciences. Coverage also extends to new experimental methods in biochemistry, theoretical contributions of biochemical importance, reviews of contemporary biochemical topics, and mini-reviews (News in Biochemistry).
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