17β-neriifolin from unripe fruits of Cerbera manghas suppressed cell proliferation via the inhibition of HOXA9-dependent transcription and the induction of apoptosis in the human AML cell line THP-1.
Shohei TakaseYoung Sook YunFuki MoriyaSaaya SekineSatoshi YotsumotoKatsunori MiyakeTadahiro YahagiAkihiro ItoHideshi InouePublished in: Journal of natural medicines (2022)
Homeobox A9 (HOXA9) is a transcription factor that is overexpressed in acute myeloid leukemia (AML). It is associated with the pathogenesis and progression of AML, and is a factor responsible for a poor prognosis. Therefore, the development of HOXA9-targeting molecules may contribute to not only better understanding of the mechanism of HOXA9 regulation, but also the development of therapeutic applications. We constructed a reporter assay system using the promoter region of the KBTBD10 gene, to which HOXA9 directly binds and regulates transcription, in the human acute monocytic leukemia cell line THP-1. Using this luciferase gene assay, we screened 1120 plant extracts and a methanol extract of the unripe fruits of Cerbera manghas was found to suppress the reporter gene expression mediated by the KBTBD10 promoter. From the extract, five steroid-type compounds were identified as the active constituents: 7α-neriifolin (1), 17β-neriifolin (2), 17α-digitoxigenin β-D-glucosyl-(1 → 4)-α-L-thevetoside (3), 17β-digitoxigenin β-D-glucosyl-(1 → 4)-α-L-thevetoside (4), and acetylthevetin B (5). Among the five compounds, 17β-neriifolin most potently inhibited HOXA9-dependent gene expression without affecting the HOXA9 mRNA levels, and suppressed cell proliferation by inducing apoptosis. The findings on the structure-activity relationships of the compounds from C. manghas may contribute to the development of small molecule inhibitors of HOXA9.
Keyphrases
- long non coding rna
- poor prognosis
- gene expression
- transcription factor
- long noncoding rna
- cell proliferation
- acute myeloid leukemia
- dna methylation
- oxidative stress
- small molecule
- endothelial cells
- genome wide
- high throughput
- cell death
- crispr cas
- endoplasmic reticulum stress
- allogeneic hematopoietic stem cell transplantation
- cell cycle
- genome wide identification
- wastewater treatment
- bone marrow
- intensive care unit
- acute respiratory distress syndrome
- liver failure
- dna binding
- carbon dioxide