CYTOTOXICITY OF LEUKEMIC CELLS BY NYPA FRUTICANS THROUGH REGULATION OF ADIPONECTIN EXPRESSION

Authors

  • MOHAMMAD FAUZAN ZAINUDIN IIUM
  • UMMU AFIFAH FADZIR IIUM
  • ATHIRAH ROSDI IIUM
  • MUHAMMAD FARID JOHAN
  • RIDZWAN HASHIM
  • RIDHWAN ABDUL WAHAB
  • SUHANA MAMAT International Islamic University Malaysia

DOI:

https://doi.org/10.31436/ijahs.v1i2.98

Abstract

Introduction: Acute lymphoblastic leukemia (ALL) is the most common leukemia subtypes among paediatrics in Malaysia. Although treatment options are available but some patients remain incurable, some undergo relapse and many experiences adverse effects by the conventional therapies. Thus, we aim to investigate possible treatment alternative by studying the antileukemogenesis properties of concentrated Nypa fruticans sap called nisaan by focusing on adiponectin expression.

Method: Our study model was CCRF-CEM, an acute lymphoblastic leukemia cell lines. The cells were treated with nisaan at a range of concentration and treated for 24, 48 and 72 hours followed by determination of the leukemic cells viability using tryphan blue method. Effective nisaan concentrations that significantly reduced the cells viability were again treated to the cells followed by determination of the cell proliferation using BrdU colorimetric kit and adiponectin level using adiponectin ELISA kit.

Results: The results showed that, increase concentration of nisaan treatment reduced the cells viability and cells proliferation and enhance the adiponectin level in the leukemic cells.

Conclusion: This preliminary data suggest that Nypa fruticans might has the anti-leukemogenesis effect on acute lymphoblastic cells by regulating the adiponectin expression.

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Published

2017-07-01

How to Cite

ZAINUDIN, M. F., FADZIR, U. A., ROSDI, A., JOHAN, M. F., HASHIM, R., ABDUL WAHAB, R., & MAMAT, S. (2017). CYTOTOXICITY OF LEUKEMIC CELLS BY NYPA FRUTICANS THROUGH REGULATION OF ADIPONECTIN EXPRESSION. INTERNATIONAL JOURNAL OF ALLIED HEALTH SCIENCES, 1(2), 28–43. https://doi.org/10.31436/ijahs.v1i2.98

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