Bioassay-Guided Isolation of 2-[p-(2-Carboxyhydrazino)phenoxy]-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol from <i>Oroxylum indicum</i> and the Investigation of Its Molecular Mechanism Action of Apoptosis Induction

The leaf crude extract of <i>Oroxylum indicum</i> (L.) Kurz induces genomic DNA fragmentation, comet formation, and the inhibition of cell proliferation in the prostate cancer cell line PC3, as assessed by agarose gel electrophoresis, comet assay and MTT assay, respectively. The bioactiv...

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Main Authors: Asem Robinson Singh (Author), Salam Asbin Singh (Author), Thangjam Davis Singh (Author), Naorem Tarundas Singh (Author), Takhellambam Chanu Machathoibi (Author), Okram Mukherjee Singh (Author), Lisam Shanjukumar Singh (Author)
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Published: MDPI AG, 2022-04-01T00:00:00Z.
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100 1 0 |a Asem Robinson Singh  |e author 
700 1 0 |a Salam Asbin Singh  |e author 
700 1 0 |a Thangjam Davis Singh  |e author 
700 1 0 |a Naorem Tarundas Singh  |e author 
700 1 0 |a Takhellambam Chanu Machathoibi  |e author 
700 1 0 |a Okram Mukherjee Singh  |e author 
700 1 0 |a Lisam Shanjukumar Singh  |e author 
245 0 0 |a Bioassay-Guided Isolation of 2-[p-(2-Carboxyhydrazino)phenoxy]-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol from <i>Oroxylum indicum</i> and the Investigation of Its Molecular Mechanism Action of Apoptosis Induction 
260 |b MDPI AG,   |c 2022-04-01T00:00:00Z. 
500 |a 10.3390/ph15050559 
500 |a 1424-8247 
520 |a The leaf crude extract of <i>Oroxylum indicum</i> (L.) Kurz induces genomic DNA fragmentation, comet formation, and the inhibition of cell proliferation in the prostate cancer cell line PC3, as assessed by agarose gel electrophoresis, comet assay and MTT assay, respectively. The bioactive compound was purified through bioassay-guided fractionation using preparative HPLC and MTT assay. The light brown and water-soluble compound was characterized using 1H and 13C nuclear magnetic resonance (NMR), Fourier transform infrared (FT-IR), and electrospray ionization (ESI) mass spectrometry. The compound was identified as a glycosylated hydroquinone derivative, 2-[p-(2-Carboxyhydrazino)phenoxy]-6-(hydroxymethyl) tetrahy-dro-2H-pyran-3,4,5-triol (molecular formula, C13H18N2O8; molecular mass = 330). The identified phytocompound has not been reported earlier elsewhere. Therefore, the common name of the novel anticancer phytocompound isolated from <i>Oroxylum indicum</i> in this current study is oroxyquinone. The half-maximal inhibitory concentration (IC<sub>50</sub>) of oroxyquinone on PC3 cells was 58.9 µM (95% CI = 54.5 to 63.7 µM). Treatment of PC3 cells with oroxyquinone induced genomic DNA fragmentation and chromatin condensation, increased in the annexin-V positive cells, arrested the cell cycle at S phases, and inhibited the cell migration; as assessed by comet assay, DAPI staining, flow cytometry and a wound healing assay, respectively. On the investigation of the molecular mechanism of the induction of apoptosis, the results indicated that oroxyquinone induced caspase-3 and PARP independent apoptosis but through the p38 pathway and the localization of AIF into the nucleus. The present study identifies a novel anticancer molecule and provides scientific evidence supporting the therapeutic potency of <i>Oroxylum indicum</i> for ethnomedicinal uses. 
546 |a EN 
690 |a <i>Oroxylum indicum</i> 
690 |a oroxyquinone 
690 |a traditional medicine 
690 |a bioassay-guided fractionation 
690 |a apoptosis 
690 |a caspase 3-independent 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 15, Iss 5, p 559 (2022) 
787 0 |n https://www.mdpi.com/1424-8247/15/5/559 
787 0 |n https://doaj.org/toc/1424-8247 
856 4 1 |u https://doaj.org/article/cfd79f44f4c04fc8af1ecca148281ba3  |z Connect to this object online.