2014•Journal of Guangxi Normal UniversityRequires access

Inhibitory Action of a Xanthono-pyridine Derivative XP-16 on Human Nasopharyngeal Carcinoma CNE Cells in vitro

Han Liu-y

Open publisher page 0 citations

Abstract

MTT assay,morphological examination and colonial assay were applied to evaluate the antiproliferative effect of a new xanthono-pyridine derivative(XP-16) on human nasopharyngeal carcinoma CNE cells;Hoechest 33258/PI double staining,flow cytometry,spectrofluorimetry and RT-PCR were also employed to investigate its possible action mechanism.The experiment results showed that XP-16 could inhibit the proliferation of CNE cells in dose- and time-dependent manner.Typical apoptotic morphology such as chromatin aggregation and nuclear fragmentation was observed in XP-16 treated CNE cells for 24 h in a dose-dependent manner.After treated with XP-16,CNE cells were blocked in G2-M and S phases,mitochondria membrane potential of the cells was decreased,relative Bad and MT-1A mRNA level was up-regulated.The apoptosis of CNE cells inducing by XP-16 might be associated with decreasing mitochondria membrane potential and up-regulating MT-1A.

About this research paper

What this paper is about

MTT assay,morphological examination and colonial assay were applied to evaluate the antiproliferative effect of a new xanthono-pyridine derivative(XP-16) on human nasopharyngeal carcinoma CNE cells;Hoechest 33258/PI double staining,flow cytometry,spectrofluorimetry and RT-PCR were also employed to investigate its possible action mechanism.The experiment results showed that XP-16 could inhibit the proliferation of CNE cells in dose- and time-dependent manner.Typical apoptotic morphology such as chromatin aggregation and nuclear fragmentation was observed in XP-16 treated CNE cells for 24 h in a dose-dependent manner.After treated with XP-16,CNE cells were blocked in G2-M and S phases,mitochondria membrane potential of the cells was decreased,relative Bad and MT-1A mRNA level was up-regulated.The apoptosis of CNE cells inducing by XP-16 might be associated with decreasing mitochondria membrane potential and up-regulating MT-1A.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

MTT assay,morphological examination and colonial assay were applied to evaluate the antiproliferative effect of a new xanthono-pyridine derivative(XP-16) on human nasopharyngeal carcinoma CNE cells;Hoechest 33258/PI double staining,flow cytometry,spectrofluorimetry and RT-PCR were also employed to investigate its possible action mechanism.The experiment results showed that XP-16 could inhibit the proliferation of CNE cells in dose- and time-dependent manner.Typical apoptotic morphology such as chromatin aggregation and nuclear fragmentation was observed in XP-16 treated CNE cells for 24 h in a dose-dependent manner.After treated with XP-16,CNE cells were blocked in G2-M and S phases,mitochondria membrane potential of the cells was decreased,relative Bad and MT-1A mRNA level was up-regulated.The apoptosis of CNE cells inducing by XP-16 might be associated with decreasing mitochondria membrane potential and up-regulating MT-1A.

Key concepts: Nasopharyngeal carcinoma, Apoptosis, Flow cytometry, Molecular biology, In vitro, MTT assay, Fragmentation (computing), Biology

Related papers

Back to paper searchBrowse research topicsOriginal source
Inhibitory Action of a Xanthono-pyridine Derivative XP-16 on Human Nasopharyngeal Carcinoma CNE Cells in vitro — Research Paper | ScholarLens