TY - JOUR
T1 - The novel herbal cocktail aga alleviates oral cancer through inducing apoptosis, inhibited migration and promotion of cell cycle arrest at subg1 phase
AU - Lu, Jui Hua
AU - Chou, Yen Ru
AU - Deng, Yue Hua
AU - Huang, Mao Suan
AU - Chien, Shaw Ting
AU - Quynh, Bach Thi Nhu
AU - Wu, Chia Yu
AU - Achtmann, Edlin Anahi Peláez
AU - Cheng, Hsin Chung
AU - Dubey, Navneet Kumar
AU - Deng, Win Ping
N1 - Funding Information:
C.-Y.W., H.-C.C., N.K.D., W.-P.D. and E.A.P.A.; Visualization, J.-H.L., Y.-R.C., Y.-H.D., S.-T.C., B.T.N.Q., C.-Y.W., C.C., N.K.D. and W.-P.D.; Methodology, J.-H.L., Y.-R.C., M.-S.H., S.-T.C., B.T.N.Q., C.-Y.W., H.-C.C., N.K.D., W.-P.D. and E.A.P.A.; Project administration, W.-P.D.; Resources, W.-P.D.; Supervision, W.-P.D.; Validation, J.-H.L., the manuscript. Y.-R.C., Y.-H.D., B.T.N.Q., C.-Y.W., H.-C.C., N.K.D., W.-P.D. and E.A.P.A.; Visualization, J.-H.L., Y.-R.C., Y.-H.D., S.-T.C., B.T.N.Q., C.-Y.W., H.-C.C., N.K.D. and E.A.P.A.; Writing—Original draft, J.-H.L., Y.-R.C., M.-S.H. Taipei Medical University (TMU 108-5601-004-111) and Stem Cell Research Center, College of Oral Medicine, and N.K.D.; Writing—Review and editing, Y.-H.D., N.K.D., W.-P.D. and E.A.P.A. All authors have read and agreed to the published version of the manuscript. Conflicts of Interest: The authors declare no conflict of interest. Funding: This research was funded by Ministry of Science and Technology Taiwan (MOST 108-2221-E-038-014), TRaeipfeerieMnecdeiscal University (TMU 108-5601-004-111) and Stem Cell Research Center, College of Oral Medicine, Taipei Medical University, Taiwan. 1. Hung, L.C.; Kung, P.T.; Lung, C.H.; Tsai, M.H.; Liu, S.A.; Chiu, L.T.; Huang, K.H.; Tsai, W.C. Assessment ConfloicfttshoefR IinstkeroefsOt:rTahl eC aauntcheorrIsn dciedcelanrcee nino AcoHnfilgicht-oRfi sinktPeroepsut.lation and Establishment of A Predictive Model for Oral Cancer Incidence Using A Population-Based Cohort in Taiwan. Int. J Environ. Res. Public Health Refer2020ence, 17s , 665. [CrossRef] 2. Yu, S.H.; Dubey, N.K.; Li, W.S.; Liu, M.C.; Chiang, H.S.; Leu, S.J.; Shieh, Y.H.; Tsai, F.C.; Deng, W.P. 1. Hung, L.C.; Kung, P.T.; Lung, C.H.; Tsai, M.H.; Liu, S.A.; Chiu, L.T.; Huang, K.H.; Tsai, W.C. Assessment Cordyceps militaris Treatment Preserves Renal Function in Type 2 Diabetic Nephropathy Mice. PLoS ONE of the Risk of Oral Cancer Incidence in A High-Risk Population and Establishment of A Predictive Model 2016, 11, e0166342. [CrossRef] [PubMed] for Oral Cancer Incidence Using A Population-Based Cohort in Taiwan. Int. J Environ. Res. Public Health 3. Liu, H.Y.; Huang, C.F.; Li, C.H.; Tsai, C.Y.; Chen, W.H.; Wei, H.J.; Wang, M.F.; Kuo, Y.H.; Cheong, M.L.; 2020, 17, 665, doi:10.3390/ijerph17020665. Deng, W.P. Osteoporosis Recovery by Antrodia camphorata Alcohol Extracts through Bone Regeneration in 2. Yu, S.H.; Dubey, N.K.; Li, W.S.; Liu, M.C.; Chiang, H.S.; Leu, S.J.; Shieh, Y.H.; Tsai, F.C.; Deng, W.P. SAMP8 Mice. Evid Based Complement. Alternat. Med. 2016, 2016, 2617868. [CrossRef] [PubMed] Cordyceps militaris Treatment Preserves Renal Function in Type 2 Diabetic Nephropathy Mice. PLoS ONE 4. Sui, Z.; Zhang, L.; Huo, Y.; Zhang, Y. Bioactive components of velvet antlers and their pharmacological 2016, 11, e0166342, doi:10.1371/journal.pone.0166342. properties. J. Pharm. Biomed. Anal. 2014, 87, 229–240. [CrossRef] [PubMed] 3. Liu, H.Y.; Huang, C.F.; Li, C.H.; Tsai, C.Y.; Chen, W.H.; Wei, H.J.; Wang, M.F.; Kuo, Y.H.; Cheong, M.L.; Deng, W.P. Osteoporosis Recovery by Antrodia camphorata Alcohol Extracts through Bone Regeneration in SAMP8 Mice. Evid Based Complement. Alternat. Med. 2016, 2016, 2617868, doi:10.1155/2016/2617868.
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/11
Y1 - 2020/11
N2 - Traditional Chinese medicines Antler’s extract (A) and Ganoderma lucidum (G) and Antrodia Camphorata (A) have been known to individually contain a plethora of bioactive factors including triterpenoids, polysaccharides etc., exerting various curative impacts such as anti-inflammatory, anti-oxidative, anti-atherosclerotic and anti-viral activities. However, their combinatorial therapeutic efficacy for oral cancer has not been investigated. Hence, we synthesized a robust cocktail called AGA and investigated its anti-oral cancer potential in vitro and in vivo. An MTT assay revealed the IC50 of AGA to be about 15 mg at 72 h. Therefore, 10 mg and 20 mg doses were selected to study the effect of AGA. The AGA significantly inhibited proliferation of oral cancer cells (HSC3, SAS, and OECM-1) in a dose-and time-dependent manner. AGA retarded cell cycle regulators (CDK4, CDK6, cyclin A, B1, D1 and E2) and apoptosis inhibitory protein Bcl-2, but enhanced pro-apoptotic protein Bax and a higher percentage of cells in Sub-G1 phase. Mechanistically, AGA suppressed all EMT markers; consequently, it decreased the migration ability of cancer cells. AGA significantly reduced xenograft tumor growth in nude mice with no adverse events in liver and renal toxicity. Conclusively, AGA strongly inhibited oral cancer through inducing apoptosis and inhibiting the migration and promotion of cell cycle arrest at subG1 phase, which may be mediated primarily via cocktail-contained triterpenoids and polysaccharides.
AB - Traditional Chinese medicines Antler’s extract (A) and Ganoderma lucidum (G) and Antrodia Camphorata (A) have been known to individually contain a plethora of bioactive factors including triterpenoids, polysaccharides etc., exerting various curative impacts such as anti-inflammatory, anti-oxidative, anti-atherosclerotic and anti-viral activities. However, their combinatorial therapeutic efficacy for oral cancer has not been investigated. Hence, we synthesized a robust cocktail called AGA and investigated its anti-oral cancer potential in vitro and in vivo. An MTT assay revealed the IC50 of AGA to be about 15 mg at 72 h. Therefore, 10 mg and 20 mg doses were selected to study the effect of AGA. The AGA significantly inhibited proliferation of oral cancer cells (HSC3, SAS, and OECM-1) in a dose-and time-dependent manner. AGA retarded cell cycle regulators (CDK4, CDK6, cyclin A, B1, D1 and E2) and apoptosis inhibitory protein Bcl-2, but enhanced pro-apoptotic protein Bax and a higher percentage of cells in Sub-G1 phase. Mechanistically, AGA suppressed all EMT markers; consequently, it decreased the migration ability of cancer cells. AGA significantly reduced xenograft tumor growth in nude mice with no adverse events in liver and renal toxicity. Conclusively, AGA strongly inhibited oral cancer through inducing apoptosis and inhibiting the migration and promotion of cell cycle arrest at subG1 phase, which may be mediated primarily via cocktail-contained triterpenoids and polysaccharides.
KW - Anti-oxidation
KW - Antler’s extract
KW - Antrodia Camphorata
KW - Cell cycle
KW - Ganoderma lucidum
KW - Oral cancer
UR - http://www.scopus.com/inward/record.url?scp=85094808287&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85094808287&partnerID=8YFLogxK
U2 - 10.3390/cancers12113214
DO - 10.3390/cancers12113214
M3 - Article
AN - SCOPUS:85094808287
SN - 2072-6694
VL - 12
SP - 1
EP - 15
JO - Cancers
JF - Cancers
IS - 11
M1 - 3214
ER -