The effect of sodium butyrate and cisplatin on expression of EMT markers

• Published in: PloS one 2019-01, Vol.14 (1), p.e0210889
• Main Authors: Mrkvicova, Alena, Chmelarova, Marcela, Peterova, Eva, Havelek, Radim, Baranova, Ivana, Kazimirova, Petra, Rudolf, Emil, Rezacova, Martina
• Format: Article
• Language: English
• Subjects: Anticancer properties; Antigens, CD - genetics; Antineoplastic Agents - pharmacology; Apoptosis; Biochemistry; Biology and life sciences; Biotechnology; Bisulfite; Butyric Acid - pharmacology; Cadherins - genetics; Cancer; Cancer cells; Carcinogenesis; Carcinogens; Care and treatment; CDH1 gene; Cell cycle; Cell Cycle - drug effects; Cell Line, Tumor; Cell Proliferation - drug effects; Chemotherapy; Cisplatin; Cisplatin - pharmacology; CpG islands; Cytotoxicity; Demethylation; Deoxyribonucleic acid; DNA; DNA methylation; Dosage and administration; Drug resistance; Drug Resistance, Neoplasm - genetics; E-cadherin; Epigenesis, Genetic - drug effects; Epigenetics; Epithelial-Mesenchymal Transition - drug effects; Epithelial-Mesenchymal Transition - genetics; Female; Gelatinase A; Gelatinase B; Gene expression; Gene Expression Regulation, Neoplastic - drug effects; Gene regulation; Gene sequencing; Genes; Genetic aspects; Genetic Markers; Histone Code - drug effects; Histone deacetylase; Histone Deacetylase Inhibitors - pharmacology; Hospitals; Humans; Medicine; Medicine and Health Sciences; Mesenchyme; Methylation; Outerwear; Ovarian cancer; Ovarian carcinoma; Ovarian Neoplasms - drug therapy; Ovarian Neoplasms - genetics; Ovarian Neoplasms - pathology; Phenotypes; Proteins; RNA polymerase; Sodium; Transcription factors; Tumors; Zinc; Zinc finger proteins
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0210889

Histone modifications play a key role in the epigenetic regulation of gene transcription in cancer cells. Histone acetylations are regulated by two classes of enzymes, histone acetyltransferases (HATs) and histone deacetylases (HDACs). HDACs are increased in ovarian carcinomas and they are involved in carcinogenesis and resistance to chemotherapeutic agents. In our study we investigated anticancer effect of HDAC inhibitor sodium butyrate (NaBu) on cisplatin-sensitive and cisplatin-resistant ovarian cell lines A2780 and A2780cis. A2780 and A2780cis were treated with NaBu alone or in combination with cisplatin (CP). NaBu inhibited the growth of both cell lines and enhanced cytotoxic effect of CP. Exposure to NaBu for 24 h induced cell cycle arrest. The expressions of EMT-related genes and proteins were further investigated by qPCR and western blot analysis. Loss of E-cadherin has been shown to be crucial in ovarian cancer development. We found that NaBu dramatically induce expression of E-cadherin gene (CDH1) and protein levels in A2780 and A2780cis. We investigated correlation between transcription and methylation of CDH1gene. Methylation level analysis in 32 CpG sites in CDH1 gene (promoter/exon1 regions) was performed using bisulfite NGS (Next Generation Sequencing). We found that cisplatin-resistant cell line A2780cis cells differ from their cisplatin-sensitive counterparts in the CDH1 methylation. Methylation in A2780cis cells is elevated compared to A2780. However, NaBu-induced expression of CDH1 was not accompanied by CDH1 demethylation. NaBu treatment induced changes in expression of EMT-related genes and proteins. Interestingly E-cadherin zinc finger transcriptional repressor SNAIL1 was upregulated in both cell lines. Mesenchymal marker vimentin was downregulated. Matrix metalloproteases (MMPs) are necessary for pericellular proteolysis and facilitate migration and invasion of tumour cells. NaBu induced mRNA expression of MMPs, mild changes in activities of gelatinases MMP2 and MMP9 were detected. Our data demonstrate that NaBu sensitizes cisplatin-resistant ovarian cancer cells, re-established E-cadherin expression, but it was not able to reverse the EMT phenotype completely.