阿霉素
三阴性乳腺癌
癌症研究
抗药性
乳腺癌
微阵列分析技术
微阵列
下调和上调
基因
癌症
药品
细胞凋亡
生物
医学
基因表达
药理学
内科学
化疗
遗传学
作者
Cristina Alexandra Ciocan-Cârtiţă,Ancuța Jurj,Oana Zănoagă,Roxana Cojocneanu,Laura Pop,Alin Moldovan,Cristian Moldovan,Alina‐Andreea Zimța,Lajos Ráduly,Cecilia Bica,Mihail Buse,Liviuţa Budişan,Piroska Virág,Alexandru Irimie,Sandra Martha Gomes Dias,Ioana Berindan‐Neagoe,Cornelia Braicu
标识
DOI:10.1186/s13046-020-01736-2
摘要
BACKGROUND: Triple negative breast cancer (TNBC) is a heterogeneous disease with aggressive behavior and an unfavorable prognosis rate. Due to the lack of surface receptors, TNBC must be intensely investigated in order to establish a suitable treatment for patients with this pathology. Chemoresistance is an important reason for therapeutic failure in TNBC. METHOD: The aim of this study was to investigate the effect of doxorubicin in TNBC cell lines and to highlight cellular and molecular alterations after a long exposure to doxorubicin. RESULTS: ) values at P12 and P24 compared to parenteral cells P0. Modifications in gene expression were investigated through microarray technique, and for detection of mutational pattern was used Next Generation Sequencing (NGS). 196 upregulated and 115 downregulated genes were observed as effect of multiple dose exposure, and 15 overexpressed genes were found to be involved in drug resistance. Also, the presence of some additional mutations in both cell lines was observed. CONCLUSION: The outcomes of this research may provide novel biomarkers for drug resistance in TNBC. Also, this activity can highlight the potential mechanisms associated with drug resistance, as well as the potential therapies to counteract these mechanisms.
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