Cytotoxic activity of eurycoma longifolia jack against nasopharyngeal carcinoma cell lines

• Main Authors: Kajahmohideen, Nur Haseena, Siti NurSyafiqah, Razi, Faisal, Ghasak Ghazi, Ashour, Abdelkader Elbadawy Abbas
• Format: Conference or Workshop Item
• Language: English; English; English
• Published: 2020
• Subjects: RB Pathology; RK318 Oral and Dental Medicine. Pathology. Diseases-Therapeutics-General Works
• Online Access: http://irep.iium.edu.my/83803/1/9th%20DSSC%20Booklet%20Done%20final.pdf; http://irep.iium.edu.my/83803/2/9th%20DSSC%20abstract.pdf; http://irep.iium.edu.my/83803/3/0BS-04%20%2817%20feb%29%20oral%20presentation%20slides%20for%20DSSC.pdf; http://irep.iium.edu.my/83803/

Introduction: Eurycoma longifolia (E. longifolia) or Tongkat Ali is a tree that grows in southeast Asia, the roots of which contains bioactive components that exhibit cytotoxic properties against various cancer cell lines. However, no study has been conducted to relate the cytotoxic properties against nasopharyngeal carcinoma (NPC), a type of cancer that shows poor prognosis for metastatic disease. The purpose of this study was to determine whether the E. longifolia root extract exerts cytotoxic activity against nasopharyngeal carcinoma (ORL-115) cell lines. Materials and method: E. longifolia root extracts were obtained through Soxhlet extraction method and by using two different solvent; ethanol and dicholoromethane. MTS assay was used to evaluate the cytotoxic effect of the root extracts against ORL-115 cell line for three different incubation time which were 24-hour, 48-hour and 72-hour. Results: Ethanol extract was significantly more potent compared to DCM extract. Ethanol extract exhibited lower IC₅₀ value compared to DCM extract. The IC₅₀ of ethanol extract were 232.1 μg/ml, 66.86 μg/ml and 42.6 μg/ml. Meanwhile the IC₅₀ of DCM extract were 678.87 μg/ml, 136.71 μg/ml, 73.72 μg/ml for 24-hour, 48-hour and 72-hour incubation period respectively. The cytotoxic activity of both extracts increased as the incubation time prolonged. The cytotoxic activity of ethanol extract at each incubation time was significantly different from DCM extract except at 72 hours. Conclusion: E. longifolia root extracts exerted cytotoxic activity against the nasopharyngeal carcinoma (ORL-115) cell line. Ethanol extract exhibited lower IC₅₀ value compared to DCM extract. The cytotoxic activity of both extracts were dose dependent and time dependent.