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In vitro anti-cancer activity of a novel microbial fermentation product on human carcinomas

  • Chung Hin Chui
  • , Roberto Gambari
  • , Fung Yi Lau
  • , Gregory Yin Ming Cheng
  • , Raymond Siu Ming Wong
  • , Stanton Hon Lung Kok
  • , Cheuk On Tang
  • , Ivy Tuang Ngo Teo
  • , Filly Cheung
  • , Chor Hing Cheng
  • , Kwok Ping Ho
  • , Albert Sun Chi Chan
  • , Alfonso Wong

Research output: Journal article publicationJournal articleAcademic researchpeer-review

Abstract

The possible anti-proliferation and cell death induction potential of a novel microbial fermentation extract named as oncogen XP-180 (or simply as XP-180) was tested on three human solid tumour carcinoma cell lines (non-small cell lung cancer A549, breast cancer MDA-MB231, liver adenocarcinoma SK-Hep1) and on the acute myelogenous leukaemia KG1a cell line. Anti-proliferative activity of XP-180 was observed on all of these cancer cell lines with comparable efficiency and in a dose-dependent manner. Morphological investigation further suggested that common features of apoptosis, including cell shrinkage and rounding, are present in XP-180 treated cells. Loss of adhesion properties of these solid tumour cell lines was observed upon XP-180 incubation. Anchorage-dependent clonogenicity assay on solid tumour cell lines and semi-solid methyl-cellulose colony formation assay on leukaemia cell line further revealed that XP-180 strongly inhibited the regeneration potential of these cancer cells. Using KG1a as an experimental model system, XP-180 was shown to stimulate the activity of caspase 3, 8 and 9 without significant change in caspase 6 activity. Furthermore, XP-180 readily induced collapse of mitochondrial membrane potential after 2 h of incubation. However, the use of the generic caspase specific inhibitor Z-VAD-FMK does not significantly reverse XP-180 mediated cell death. The results obtained suggest that XP-180-mediated cancer cell death could involve mitochondria and both caspase-dependent and -independent pathways. Therefore, XP-180 is an efficient anti-cancer regimen in vitro.
Original languageEnglish
Pages (from-to)675-679
Number of pages5
JournalInternational Journal of Molecular Medicine
Volume17
Issue number4
Publication statusPublished - 1 Apr 2006

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Apoptosis
  • Neoplasms
  • Oncogen XP-180

ASJC Scopus subject areas

  • Genetics

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