Effect of three fatty acids from the leaf extract of Tiliacora triandra on P‑glycoprotein function in multidrug‑resistant A549RT‑eto cell line
Chutima Kaewpiboon1, Pakorn Winayanuwattikun2, Tikamporn Yongvanich2, Preecha Phuwapraisirisan3, Wanchai Assavalapsakul4★★ Corresponding author
- 1Department of Biology, Faculty of Science, Thaksin University, Phatthalung 93110, Departments of, Thailand.
- 2Biochemistry, Thailand.
- 3Chemistry and, Thailand.
- 4Microbiology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.
CORRESPONDENCE
Wanchai Assavalapsakul
Microbiology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.
Received: 06-12-2013; Revised: 17-02-2014.
Volume 10, Issue 39s · pp. 549–556 · PUBLISHED 2014 · DOI: 10.4103/0973-1296.139779
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ABSTRACT
Background: Cancer cells have the ability to develop resistance to chemotherapy drugs, which then leads to a reduced effectiveness and success of the treatment. Multidrug resistance (MDR) involves the resistance in the same cell/tissue to a diverse range of drugs of different structures. One of the characteristics of MDR is an overexpression of P‑glycoprotein (P‑gp), which causes the efflux of the accumulated drug out of the cell. The MDR human non‑small cell lung carcinoma cell line with a high P‑gp expression level (A549RT‑eto) was used to investigate the bioactive compounds capable of reversing the etoposide resistance in this cell line. Materials and Methods: The leaves of Tiliacora triandra were sequentially extracted with hexane, dichloromethane, methanol and water. Only the hexane extract reduced the etoposide resistance of the A549RT‑eto cell line, and was further fractionated by column chromatography using the TLC‑pattern and the restoration of etoposide sensitivity as the selection criteria. Results: The obtained active fraction (F22) was found by nuclear magnetic resonance and gas chromatography‑mass spectroscopy analyses to be comprised of a 49.5:19.6:30.9 (w/w/w) mixture of hexadecanoic: octadecanoic acid: (Z)‑6‑octadecenoic acids. This stoichiometric mixture was recreated using pure fatty acids (MSFA) and gave a similar sensitization to etoposide and enhanced the relative rate of rhodamine‑123 accumulation to a similar extent as F22, supporting the action via reducing P‑gp activity. In contrast, the fatty acids alone did not show this effect. Conclusion: This is the first report of the biological activity from the leaves of T. triandra as a potential source of a novel chemosensitizer.
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Kaewpiboon, C., Winayanuwattikun, P., Yongvanich, T., Phuwapraisirisan, P., & Assavalapsakul, W. (2014). Effect of three fatty acids from the leaf extract of Tiliacora triandra on P‑glycoprotein function in multidrug‑resistant A549RT‑eto cell line. Pharmacognosy Magazine, 10(39s), 549–556. https://doi.org/10.4103/0973-1296.139779
