Abstract
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.
| Original language | English |
|---|---|
| Article number | 2495 |
| Journal | Molecules |
| Volume | 24 |
| Issue number | 13 |
| DOIs | |
| Publication status | Published - Jan 1 2019 |
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Keywords
- 5,6-dehydrokawain
- Alpinia zerumbet
- Anti-oxidant
- Anti-tumor
- Ehrlich ascites carcinoma
ASJC Scopus subject areas
- Analytical Chemistry
- Chemistry (miscellaneous)
- Molecular Medicine
- Pharmaceutical Science
- Drug Discovery
- Physical and Theoretical Chemistry
- Organic Chemistry
Cite this
Alpinia zerumbet (Pers.) : Food and medicinal plant with potential in vitro and in vivo anti-cancer activities. / Maram, Hussein; Salem, Tarek A.R.; El-Aarag, Bishoy; Yosri, Nermeen; EL-Ghlban, Samah; Zaki, Kholoud; Marei, Amel H.; El-Wahed, Aida Abd; Saeed, Aamer; Khatib, Alfi; AlAjmi, Mohamed F.; Shathili, Abdulrahman M.; Xiao, Jianbo; Khalifa, Shaden A.M.; El-Seedi, Hesham R.
In: Molecules, Vol. 24, No. 13, 2495, 01.01.2019.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Alpinia zerumbet (Pers.)
T2 - Food and medicinal plant with potential in vitro and in vivo anti-cancer activities
AU - 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.
PY - 2019/1/1
Y1 - 2019/1/1
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
UR - http://www.scopus.com/inward/record.url?scp=85068848824&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85068848824&partnerID=8YFLogxK
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 -