Gumbarewicz Ewelina, Tylżanowski Przemko, Łuszczki Jarogniew, Kałafut Joanna, Czerwonka Arkadiusz, Szumiło Justyna, Wawruszak Anna, Kupisz Krzysztof, Polberg Krzysztof, Smok-Kalwat Jolanta, Stepulak Andrzej
Department of Biochemistry and Molecular Biology, Medical University of Lublin Chodzki 1 St., 20-093 Lublin, Poland.
Laboratory for Developmental and Stem Cell Biology, Department of Development and Regeneration, Skeletal Biology and Engineering Research Centre, University of Leuven Leuven, Belgium.
Am J Cancer Res. 2021 Jun 15;11(6):2821-2837. eCollection 2021.
Successful treatment of advanced larynx squamous cell carcinoma (LSCC) remains a challenge, mainly due to limited response to chemotherapy and the phenomenon of the drug resistance. Therefore, new chemotherapeutic solutions are needed. The aim of this study was to explore benefit of combined cisplatin (CDDP) and valproic acid (VPA) therapy in patients' derived LSCC cell lines. Cell viability assay was used to establish cellular response to the drug by isobolography followed by RNA sequencing (RNAseq) analysis. were used for studies. Depending on the cell line, we found that the combinations of drugs resulted in synergistic or antagonistic pharmacological interaction, which was accompanied by significant changes in genes expression profiles. The presented therapeutic scheme efficiently blocked tumor growth in an model, corresponding to the in vitro performed studies. Interestingly the RK5 cell line, upon the combined treatment acquired a molecular profile typically associated with epithelial to mesenchymal transition (EMT). Hence, our studies demonstrates that patient-specific personalized therapy of larynx cancer should be considered and the combination of cisplatin and valproic acid should be explored as a potential therapeutic strategy in the treatment of larynx cancer.
晚期喉鳞状细胞癌(LSCC)的成功治疗仍然是一项挑战,主要原因是化疗反应有限以及耐药现象。因此,需要新的化疗方案。本研究的目的是探讨顺铂(CDDP)和丙戊酸(VPA)联合治疗对源自患者的LSCC细胞系的益处。通过等效线图法建立细胞对药物的反应,随后进行RNA测序(RNAseq)分析,以进行细胞活力测定研究。根据细胞系,我们发现药物组合导致协同或拮抗的药理相互作用,并伴随着基因表达谱的显著变化。所提出的治疗方案在动物模型中有效地阻断了肿瘤生长,这与体外实验结果相符。有趣的是,RK5细胞系在联合治疗后获得了通常与上皮-间质转化(EMT)相关的分子特征。因此,我们的研究表明,应考虑针对喉癌患者的个性化治疗,并探索顺铂和丙戊酸联合作为喉癌治疗的潜在策略。