S100A6诱导EGFR 19外显子突变的人肺腺癌PC9细胞系对吉非替尼的耐药性

IF 2.6 4区 医学 Q3 ONCOLOGY
Cancer Management and Research Pub Date : 2025-09-29 eCollection Date: 2025-01-01 DOI:10.2147/CMAR.S533644
Ting Wang, Xiaoai Shou
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引用次数: 0

摘要

简介:S100钙结合蛋白A6 (S100A6)已被证实参与了包括肺腺癌(LADC)在内的多种恶性肿瘤的发生发展。S100A6对癌细胞耐药的影响尚不清楚。EGFR 19外显子突变的PC9细胞常用于肺癌细胞实验。方法:成功构建过表达S100A6的PC9细胞(PC9/S100A6),同时设PC9细胞为对照组。采用MTT法检测和比较两组细胞在吉非替尼、顺铂、培美曲塞、贝伐单抗不同浓度和时间点的生长速率。结果:数据显示,吉非替尼(0.01µmol/L、0.1µmol/L、1µmol/L)对PC9/S100A6细胞的抑制率在24h、48h、72h显著降低(p)。结论:S100A6能明显促进EGFR 19外显子突变的LADC PC9细胞株对吉非替尼的抗性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

S100A6 Induces the Resistance to Gefitinib in Human Lung Adenocarcinoma PC9 Cell Lines with EGFR 19 Exon Mutations.

S100A6 Induces the Resistance to Gefitinib in Human Lung Adenocarcinoma PC9 Cell Lines with EGFR 19 Exon Mutations.

S100A6 Induces the Resistance to Gefitinib in Human Lung Adenocarcinoma PC9 Cell Lines with EGFR 19 Exon Mutations.

Introduction: S100 calcium binding protein A6 (S100A6) has been confirmed to be involved in the occurrence and development of various malignant tumors, including lung adenocarcinoma (LADC). The impact of S100A6 on the drug resistance of cancer cell lines is still uncovered. PC9 cells with EGFR 19 exon mutation is commonly used in lung cancer cell experiments.

Methods: In this work, PC9 cells over-expressing S100A6 (PC9/S100A6) was successfully constructed, and the PC9 cells were set as control group simultaneously. MTT assay was used to detect and compare the growth rates of the cells in two groups at different concentrations and time points of gefitinib, cisplatin, pemetrexed, bevacizumab.

Results: Data showed that the inhibitory rates of gefitinib (0.01µmol/L, 0.1µmol/L, 1µmol/L) on PC9/S100A6 cells significantly decreased at 24h, 48h, 72h (P<0.05). Additionally, the inhibitory effects on PC9/S100A6 cells were significantly lower for 10 µmol/L gefitinib (at 48h and 72h), 100 µmol/L gefitinib (at 72h), 2.5 µg/mL cisplatin (at 48h and 72h), and 10 µg/mL cisplatin (at 72h). However, there is no obvious difference in the inhibitory rate of cisplatin (2.5µg/mL 24h; 10µg/mL 24h, 48h; 5µg/mL, 20µg/mL, 40µg/mL 24h, 48h, and 72h), pemetrexed, bevacizumab on two groups.

Conclusion: Our results demonstrated that S100A6 can apparently promote the resistance to gefitinib of LADC PC9 cell lines with EGFR 19 exon mutations.

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来源期刊
Cancer Management and Research
Cancer Management and Research Medicine-Oncology
CiteScore
7.40
自引率
0.00%
发文量
448
审稿时长
16 weeks
期刊介绍: Cancer Management and Research is an international, peer reviewed, open access journal focusing on cancer research and the optimal use of preventative and integrated treatment interventions to achieve improved outcomes, enhanced survival, and quality of life for cancer patients. Specific topics covered in the journal include: ◦Epidemiology, detection and screening ◦Cellular research and biomarkers ◦Identification of biotargets and agents with novel mechanisms of action ◦Optimal clinical use of existing anticancer agents, including combination therapies ◦Radiation and surgery ◦Palliative care ◦Patient adherence, quality of life, satisfaction The journal welcomes submitted papers covering original research, basic science, clinical & epidemiological studies, reviews & evaluations, guidelines, expert opinion and commentary, and case series that shed novel insights on a disease or disease subtype.
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