TY - JOUR
T1 - Alpinia zerumbet (Pers.)
T2 - Food and medicinal plant with potential in vitro and in vivo anti-cancer activities
AU - Zahra, Maram Hussein
AU - Salem, Tarek A.R.
AU - El-Aarag, Bishoy
AU - Yosri, Nermeen
AU - EL-Ghlban, Samah
AU - Zaki, Kholoud
AU - Marei, Amel H.
AU - El-Wahed, Aida Abd
AU - Saeed, Aamer
AU - Khatib, Alfi
AU - AlAjmi, Mohamed F.
AU - Shathili, Abdulrahman M.
AU - Xiao, Jianbo
AU - Khalifa, Shaden A.M.
AU - El-Seedi, Hesham R.
N1 - Funding Information:
Funding: The authors wish to express their appreciation to the International Scientific Partnership Program (ISPP) at King Saud University for funding this research work through an ISPP-126 grant awarded to H.R.E. and M.F.E. H.R.E. Alfi Khatib wish to thank the International Islamic University Malaysia for the Publication Research Initiative Grant Fund (PRIGS18-027-0027). wishes to thank the Swedish Research links grant 2016-05885 (VR for the years 2017–2019) for financial support.
PY - 2019
Y1 - 2019
N2 - Background/Aim: Plants play an important role in anti-cancer drug discovery, therefore, the current study aimed to evaluate the biological activity of Alpinia zerumbet (A. zerumbet) flowers. Methods: The phytochemical and biological criteria of A. zerumbet were in vitro investigated as well as in mouse xenograft model. Results: A. zerumbet extracts, specially CH2Cl2 and MeOH extracts, exhibited the highest potent anti-tumor activity against Ehrlich ascites carcinoma (EAC) cells. The most active CH2Cl2 extract was subjected to bioassay-guided fractionation leading to isolatation of the naturally occurring 5,6-dehydrokawain (DK) which was characterized by IR, MS, 1H-NMR and 13C-NMR. A. zerumbet extracts, specially MeOH and CH2Cl2 extracts, exhibited significant inhibitory activity towards tumor volume (TV). Furthermore, A. zerumbet extracts declined the high level of malonaldehyde (MDA) as well as elevated the levels of superoxide dismutase (SOD) and catalase (CAT) in liver tissue homogenate. Moreover, DK showed anti-proliferative action on different human cancer cell lines. The recorded IC50 values against breast carcinoma (MCF-7), liver carcinoma (Hep-G2) and larynx carcinoma cells (HEP-2) were 3.08, 6.8, and 8.7 µg/mL, respectively. Conclusion: Taken together, these findings open the door for further investigations in order to explore the potential medicinal properties of A. zerumbet.
AB - Background/Aim: Plants play an important role in anti-cancer drug discovery, therefore, the current study aimed to evaluate the biological activity of Alpinia zerumbet (A. zerumbet) flowers. Methods: The phytochemical and biological criteria of A. zerumbet were in vitro investigated as well as in mouse xenograft model. Results: A. zerumbet extracts, specially CH2Cl2 and MeOH extracts, exhibited the highest potent anti-tumor activity against Ehrlich ascites carcinoma (EAC) cells. The most active CH2Cl2 extract was subjected to bioassay-guided fractionation leading to isolatation of the naturally occurring 5,6-dehydrokawain (DK) which was characterized by IR, MS, 1H-NMR and 13C-NMR. A. zerumbet extracts, specially MeOH and CH2Cl2 extracts, exhibited significant inhibitory activity towards tumor volume (TV). Furthermore, A. zerumbet extracts declined the high level of malonaldehyde (MDA) as well as elevated the levels of superoxide dismutase (SOD) and catalase (CAT) in liver tissue homogenate. Moreover, DK showed anti-proliferative action on different human cancer cell lines. The recorded IC50 values against breast carcinoma (MCF-7), liver carcinoma (Hep-G2) and larynx carcinoma cells (HEP-2) were 3.08, 6.8, and 8.7 µg/mL, respectively. Conclusion: Taken together, these findings open the door for further investigations in order to explore the potential medicinal properties of A. zerumbet.
KW - 5,6-dehydrokawain
KW - Alpinia zerumbet
KW - Anti-oxidant
KW - Anti-tumor
KW - Ehrlich ascites carcinoma
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U2 - 10.3390/molecules24132495
DO - 10.3390/molecules24132495
M3 - Article
C2 - 31288458
AN - SCOPUS:85068848824
VL - 24
JO - Molecules
JF - Molecules
SN - 1420-3049
IS - 13
M1 - 2495
ER -