Effects of Hexane Root Extract of Ferula hermonis Boiss. on Human Breast and Colon Cancer Cells: An In Vitro and In Vivo Study

被引:18
作者
Abutaha, Nael [1 ]
Nasr, Fahd A. [2 ]
Al-zharani, Mohammed [3 ]
Alqahtani, Ali S. [2 ]
Noman, Omar M. [2 ]
Mubarak, Mohammed [4 ]
Abdelhabib, Semlali [5 ]
Wadaan, Muhammad A. [1 ]
机构
[1] King Saud Univ, Coll Sci, Dept Zool, Riyadh, Saudi Arabia
[2] King Saud Univ, Coll Pharm, Med Aromat & Poisonous Plants Res Ctr, Riyadh 11451, Saudi Arabia
[3] Al Imam Mohammad Ibn Saud Islamic Univ IMSIU, Coll Sci, Dept Biol, Riyadh, Saudi Arabia
[4] King Saud Univ Med City, Electron Microscope Unit, Riyadh, Saudi Arabia
[5] Univ Laval, Fac Med Dent, Grp Rech Ecol Buccale, Quebec City, PQ, Canada
关键词
BACCATIN III; DAUCANE SESQUITERPENES; NATURAL-PRODUCTS; ALPHA-PINENE; APOPTOSIS; PRECURSOR; LINE; CYTOTOXICITY; ANTICANCER; FERUTININ;
D O I
10.1155/2019/3079895
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Breast and colon cancers are leading causes of cancer-related deaths globally. Plants are a potential source of natural products that may be used for the treatment of cancer. Ferula hermonis (FH) is reported to have diverse therapeutic effects. However, there are few reports on the in vitro anticancer potential of FH extract. Our results showed that the Ferula hermonis root hexane extract (FHRH) can induce dose-dependent cytotoxic effects in breast and colon cancer cells with MTT IC50 values of 18.2 and 25 mu g/ml, respectively. The FHRH extract induced apoptosis in both breast and colon cancer cells; this was confirmed by light and nuclear staining, q-PCR, and caspase 3/7 activation. This study also demonstrated the antitumor activity of FHRH in 9,10-dimethylbenz[alpha]anthracene DMBA-induced rodent mammary tumor model. The GC/MS analysis revealed the presence of 3,5-Dimethylbenzenemethanol, Alpha-Bisabolol, Alpha-pinene, Beta-pinene, and Baccatin III that have various pharmacological potentials. Overall, the present study suggests that FHRH extract possesses anticancer potential which is mediated through apoptotic effects in MDA-MB-231 and LoVo cells. The present study also considered a basis for further investigations into the potential use of FHRH extract as an anticancer therapy for breast and colon cancers.
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页数:12
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共 53 条
  • [1] Apoptotic Potential of Artemsia sieberia Besser (Asteraceae) Fraction against Human Cancer Cell Lines
    Abutaha, Nael
    Mashaly, Ashraf M. A.
    Farooq, Muhammad
    Wadaan, Muhammad A.
    [J]. TROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH, 2015, 14 (10) : 1779 - 1785
  • [2] A major constituent of green tea, EGCG, inhibits the growth of a human cervical cancer cell line, CaSki cells, through apoptosis, G1 arrest, and regulation of gene expression
    Ahn, WS
    Huh, SW
    Bae, SM
    Lee, IP
    Lee, JM
    Namkoong, SE
    Kim, CK
    Sin, JI
    [J]. DNA AND CELL BIOLOGY, 2003, 22 (03) : 217 - 224
  • [3] Antifungal Compounds from the Rhizome and Roots of Ferula hermonis
    Al-Ja'fari, Abdel-Hadi
    Vila, Roser
    Freixa, Blanca
    Costa, Joan
    Canigueral, Salvador
    [J]. PHYTOTHERAPY RESEARCH, 2013, 27 (06) : 911 - 915
  • [4] Study of the cytotoxicity of asiaticoside on rats and tumour cells
    Al-Saeedi, Fatma J.
    [J]. BMC CANCER, 2014, 14
  • [5] Amin Amr, 2009, Int J Biomed Sci, V5, P1
  • [6] In Vitro Antioxidant and Anticancer Activity Studies on Drosera Indica L. (Droseraceae)
    Asirvatham, Raju
    Christina, Arockiasamy Josphin Maria
    Murali, Anita
    [J]. ADVANCED PHARMACEUTICAL BULLETIN, 2013, 3 (01) : 115 - 120
  • [7] Feruhermonins A-C:: three daucane esters from the seeds of Ferula hermonis (Apiaceae)
    Auzi, Abdurazag A.
    Gray, Alexander I.
    Salem, Mohamed M.
    Badwan, Adnan A.
    Sarker, Satyajit D.
    [J]. JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2008, 10 (08) : 701 - 707
  • [8] Antioxidative, anticancer and genotoxic properties of α-pinene on N2a neuroblastoma cells
    Aydin, Elanur
    Turkez, Hasan
    Geyikoglu, Fatime
    [J]. BIOLOGIA, 2013, 68 (05) : 1004 - 1009
  • [9] Bazarbashi Shouki, 2017, Asian Pac J Cancer Prev, V18, P2437, DOI 10.22034/APJCP.2017.18.9.2437
  • [10] Blaskovich MA, 2003, CANCER RES, V63, P1270