African Journal of
Biotechnology

  • Abbreviation: Afr. J. Biotechnol.
  • Language: English
  • ISSN: 1684-5315
  • DOI: 10.5897/AJB
  • Start Year: 2002
  • Published Articles: 12506

Full Length Research Paper

Clausenidin upregulated p53 and caused apoptosis in HT-29 tumor cell lines

Peter M. Waziri
  • Peter M. Waziri
  • MAKNA Cancer Research Laboratory, Institute of Bioscience, University Putra Malaysia, Serdang, Selangor, Malaysia.
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Rasedee Abdullah
  • Rasedee Abdullah
  • Department of Veterinary Pathology and Microbiology, Faculty of Veterinary, University Putra Malaysia, Serdang, Selangor, Malaysia.
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Rosita Rosli
  • Rosita Rosli
  • MAKNA Cancer Research Laboratory, Institute of Bioscience, University Putra Malaysia, Serdang, Selangor, Malaysia.
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Abdul Rahman Omar
  • Abdul Rahman Omar
  • Laboratory of Vaccine and Therapeutics, Institute of Bioscience, University Putra Malaysia, Serdang, Selangor, Malaysia.
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Ahmad Bustamam Abdul
  • Ahmad Bustamam Abdul
  • MAKNA Cancer Research Laboratory, Institute of Bioscience, University Putra Malaysia, Serdang, Selangor, Malaysia.
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Nur Kartinee Kassim
  • Nur Kartinee Kassim
  • Department of Chemistry, Faculty of Science, University Putra Malaysia, Serdang, Selangor, Malaysia.
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Ibrahim Malami
  • Ibrahim Malami
  • MAKNA Cancer Research Laboratory, Institute of Bioscience, University Putra Malaysia, Serdang, Selangor, Malaysia.
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Imaobong C. Etti
  • Imaobong C. Etti
  • MAKNA Cancer Research Laboratory, Institute of Bioscience, University Putra Malaysia, Serdang, Selangor, Malaysia.
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Palanisamy Arulselvan
  • Palanisamy Arulselvan
  • Laboratory of Vaccine and Therapeutics, Institute of Bioscience, University Putra Malaysia, Serdang, Selangor, Malaysia.
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Ashwaq Shakir Al-Abboodi
  • Ashwaq Shakir Al-Abboodi
  • MAKNA Cancer Research Laboratory, Institute of Bioscience, University Putra Malaysia, Serdang, Selangor, Malaysia.
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  •  Received: 07 June 2018
  •  Accepted: 17 July 2018
  •  Published: 19 December 2018

Abstract

Clausenidin is a pyranocoumarin majorly found in medicinal herbs of the Rutaceae family used to treat cancer patients locally in Asia. The compound is presumed to have anti-cancer cell effect but its exact mechanism of action is still unknown. The study aimed to evaluate the effect of pure clausenidin on p53-mediated apoptosis as well as other cell death pathways in colon cancer (HT-29) cell lines. The anti-proliferative effect of clausenidin by cell cycle and annexin V assay using flow cytometry was evaluated. Morphological analysis of the treated cells was performed using scanning and transmission electron microscopy. Furthermore, the effect of p53 mRNA on cell cycle and apoptosis-related genes and proteins in clausenidin-treated HT-29 cells was investigated using qPCR and Western blot assays, respectively. Clausenidin induced a p53 dependent G0/G1 cell cycle arrest in HT-29 cells. It was also observed that the anti-cancer cell effect of clausenidin occurred via p53 mediated activation of p21, bax and transrepression of survivin and bcl 2 that culminated in the apoptosis of colon cancer cells. The transmission electron microscopy (TEM) micrographs confirmed the occurrence of apoptosis in clausenidin-treated HT-29 cells. Clausenidin is a potent anti-HT-29 cell agent that can be used to treat colon tumors.

 

Key words: Clausenidin, p53, p21, apoptosis, cell cycle.