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In Vitro Antiproliferative Activity of Fresh Pineapple Juices on Ovarian and Colon Cancer Cell Lines

  • Madihah Binti Abdul Gani
  • Rozita Nasiri
  • Javad Hamzehalipour Almaki
  • Fadzilah Adibah Abdul MajidEmail author
  • Mohsen Marvibaigi
  • Neda Amini
  • Siavash Hosseinpour Chermahini
  • Mirdawati Mashudin
Article

Abstract

The main component that contributes to the high value of pineapple is bromelain which is a proteolytic enzyme and has been scientifically identified as a therapeutic agent. This study was conducted to obtain high quantity of bromelain from pineapple and to investigate the anticarcinogenic activity of fresh pineapple juices against A2780 ovarian and HT29 colon cancer cell lines. It was found that homogenization, ultrafiltration, precipitation and dialysis contributed to heavy loss of bromelain. Therefore, fresh pineapple juices from the flesh (PJ-F), core (PJ-C) and stem (PJ-S) were selected as a source of crude bromelain. Various bromelain concentrations of PJ-F, PJ-C and PJ-S (1 μg/ml, 10 μg/ml, 100 μg/ml and 1000 μg/ml) were exposed to the cancer cells and the cell viability was determined using Methylthiazol Tetrazolium Assay (MTT assay) after 24, 48 and 72 h. Besides, IC50 values were measured. Using normal cell (HSF1184) comparison, it was found that a 100 μg/ml concentration of bromelain would efficiently inhibit the cancer cells without affecting the surrounding normal cells. Microscopic examinations were carried out to elucidate the modes of cell death on the basis of morphological alterations using florescent and inverted phase contrast microscopes. Furthermore, the colony forming abilities of fresh pineapple juices on A2780 and HT29 cells were examined. The results demonstrated that PJ-F, PJ-C and PJ-S effectively suppressed the colony formation in cancer cells. The findings suggest that PJ-F, PJ-C and PJ-S may have the potential to induce anticarcinogenic effects through an apoptosis to A2780 and HT29 cells in vitro.

Keywords

Bromelain Fresh pineapple juice Anticarcinogenic Colon cancer Ovarian cancer 

Notes

Acknowledgments

We are sincerely grateful to Prof. Madya Dr. Fadzilah Adibah binti Abd Majid for her excellent assistance in entire research procedure. This research was supported by Biotechnology Research Alliance, Institute of Bioproduct Development (IBD), Universiti Teknologi Malaysia, UTM 81310, Johor Bahru, Johor, Malaysia.

Conflict of interest

All the authors declare that there is no conflict of interest.

Human and Animal Rights and Informed Consent

This article does not contain any studies with human or animal subjects performed by any of the authors.

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Copyright information

© Springer Science+Business Media New York 2015

Authors and Affiliations

  • Madihah Binti Abdul Gani
    • 1
  • Rozita Nasiri
    • 1
  • Javad Hamzehalipour Almaki
    • 1
  • Fadzilah Adibah Abdul Majid
    • 1
    • 3
    Email author
  • Mohsen Marvibaigi
    • 2
  • Neda Amini
    • 2
  • Siavash Hosseinpour Chermahini
    • 1
  • Mirdawati Mashudin
    • 1
  1. 1.Department of Bioprocess Engineering, Faculty of Chemical EngineeringUniversiti Teknologi MalaysiaJohor BahruMalaysia
  2. 2.IJN-UTM Cardiovascular Engineering Center, Faculty of Biosciences and Medical EngineeringUniversiti Teknologi MalaysiaSkudaiMalaysia
  3. 3.Biotechnology Research Alliance, Institute OF Bioproduct Development (IBD)Universiti Teknologi MalaysiaJohor BahruMalaysia

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