Browse > Article
http://dx.doi.org/10.7314/APJCP.2015.16.14.6117

Anticancer Potential of Cratoxylum formosum Subsp. Pruniflorum (Kurz.) Gogel Extracts Against Cervical Cancer Cell Lines  

Promraksa, Bundit (Department of Biochemistry, Medicine, Khon Kaen University)
Daduang, Jureerut (Centre for Research and Development of Medical Diagnostic Laboratories, Khon Kaen University)
Khampitak, Tueanjit (Department of Biochemistry, Medicine, Khon Kaen University)
Tavichakorntrakool, Ratree (Centre for Research and Development of Medical Diagnostic Laboratories, Khon Kaen University)
Koraneekit, Amonrat (Centre for Research and Development of Medical Diagnostic Laboratories, Khon Kaen University)
Palasap, Adisak (Centre for Research and Development of Medical Diagnostic Laboratories, Khon Kaen University)
Tangrassameeprasert, Roongpet (Department of Biochemistry, Medicine, Khon Kaen University)
Boonsiri, Patcharee (Department of Biochemistry, Medicine, Khon Kaen University)
Publication Information
Asian Pacific Journal of Cancer Prevention / v.16, no.14, 2015 , pp. 6117-6121 More about this Journal
Abstract
Background: Most northeast Thai vegetables may play roles in human health by acting as antioxidant and anticancer agents. Recent study showed that Cratoxylum formosum subsp. pruniflorum (Kurz.) Gogel. (Teawdang) could inhibit growth of liver cancer cell lines. Cervical cancer, which has human papilloma virus as its main cause, is found at high incidence in Thailand. Due to increasing drug resistance, searches for potential anticancer compounds from natural source are required. Therefore, our purpose was to evaluate the cytotoxicity of Teawdang extracts in cervical cancer cell lines. Materials and Methods: Teawdang edible parts, purchased from Khon Kaen market during July-October 2013 was extracted with organic solvent. Phenolic profiles of crude hexane (CHE), ethyl acetate (CEE), methanol (CME) and water (CWE) extracts were performed by high performance liquid chromatographic (HPLC) techniques. Their cytotoxic effects on cervical cancer cells were investigated with HPV-non infected (C-33A) and HPV-infected (HeLa and SiHa) cell lines. Results: HPLC profiles showed that all crude extracts contained caffeine, ferulic acid and resveratrol. CME and CEE had high contents of gallic acid and quercetin. Catechin was found only in CWE. Cytotoxicity test showed that CEE had the lowest IC50 on HeLa ($143.18{\pm}13.35 {\mu}g/mL$) and SiHa cells ($106.45{\pm}15.73{\mu}g/mL$). C-33A cells were inhibited by CWE ($IC50=130.95{\pm}3.83{\mu}g/mL$). Conclusions: There were several phenolic compounds in Teawdang extracts which may have cytotoxic effects on cervical cancer cell lines. Investigation of these bioactive compounds as new sources of anticancer agents is recommended.
Keywords
Cervical cancer; Cratoxylum formosum subsp. pruniflorum (Kurz.) Gogel., cytotoxic effect; phenolics;
Citations & Related Records
Times Cited By KSCI : 3  (Citation Analysis)
연도 인용수 순위
1 Daduang J, Vichitphan S, Daduang S, et al (2011). High phenolics and antioxidants of some tropical vegetables related to antibacterial and anticancer activities. Afr J Pharm Pharmacol, 5, 608-15.   DOI
2 Daneshfar A, Ghaziaskar HS, Homayoun N (2008). Solubility of gallic acid in methanol, ethanol, water, and ethyl acetate. J Chem Eng Data, 53, 776-8.   DOI
3 Di Domenico F, Foppoli C, Coccia R, et al (2012). Antioxidants in cervical cancer: chemopreventive and chemotherapeutic effects of polyphenols. Biochim Biophys Acta, 1822, 737-47.   DOI
4 Dung TT, Lee J, Kim E, et al (2015). Anti-inflammatory activities of Gouania leptostachya methanol extract and its constituent resveratrol. Phytother Res, 29, 381-92.   DOI
5 Ferlay J, Soerjomataram I, Ervik M, et al (2013). GLOBOCAN 2008 V1.2. GLOBOCAN 2012 v1.0, Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 11 (Internet). globocan.iarc.fr.
6 Khuhaprema T, Srivatanakul P, Sriplung H, et al (2007). Cancer in Thailand: Vol. VII, 2007-2009. Bangkok: Bangkok Medical Publisher.
7 Lee JH, Cho S, Paik HD, et al (2014). Investigation on antibacterial and antioxidant activities, phenolic and flavonoid contents of some Thai edible plants as an alternative for antibiotics. Asian-Australas J Anim Sci, 27, 1461-8.   DOI
8 Machana S, Weerapreeyakul N, Barusrux S, et al (2011). Cytotoxic and apoptotic effects of six herbal plants against the human hepatocarcinoma (HepG2) cell line. Chin Med, 6, 39.   DOI
9 Maisuthisakul P, Pongsawatmanit R, Gordon MH (2006). Antioxidant properties of Teaw (Cratoxylum formosum Dyer) extract in soybean oil and emulsions. J Agric Food Chem, 54, 2719-25.   DOI
10 Boonsri S, Karalai C, Ponglimanont C, et al (2006). Antibacterial and cytotoxic xanthones from the roots of Cratoxylum formosum. Phytochemistry, 67, 723-7.   DOI
11 Britten RA, Liu D, Tessier A, et al (2000). ERCC1 expression as a molecular marker of cisplatin resistance in human cervical tumor cells. Int J Cancer, 89, 453-7.   DOI
12 Maisuthisakul P, Pongsawatmanit R, Gordon MH (2007). Characterization of the phytochemicals and antioxidant properties of extracts from Teaw (Cratoxylum formosum Dyer). Food Chem, 100, 1620-9.   DOI
13 Martinho O, Pinto F, Granja S, et al (2013). RKIP inhibition in cervical cancer is associated with higher tumor aggressive behavior and resistance to cisplatin therapy. PLoS One, 8, 59104.   DOI
14 Nonpunya A, Weerapreeyakul N, Barusrux S (2014). Cratoxylum formosum (Jack) Dyer ssp. pruniflorum (Kurz) Gogel. (Hong ya mu) extract induces apoptosis in human hepatocellular carcinoma HepG2 cells through caspase-dependent pathways. Chin Med, 9, 12.   DOI
15 Palasap A, Limpaiboon T, Boonsiri P, et al (2014). Cytotoxic efects of phytophenolics from Caesalpinia mimosoides Lamk on cervical carcinoma cell lines through an apoptotic pathway. Asian Pac J Cancer Prev, 15, 449-54.   DOI   ScienceOn
16 Romagnolo DF, Selmin OI (2012). Flavonoids and cancer prevention: a review of the evidence. J Nutr Gerontol Geriatr, 31, 206-38.   DOI
17 Sak K (2012). Chemotherapy and dietary phytochemical agents. Chemother Res Pract, 2012, 282570.
18 Saxena A, Yashar C, Taylor DD, et al (2005). Cellular response to chemotherapy and radiation in cervical cancer. Am J Obstet Gynecol, 192, 1399-403.   DOI
19 Shen DW, Pouliot LM, Hall MD, et al (2012). Cisplatin resistance: a cellular self-defense mechanism resulting from multiple epigenetic and genetic changes. Pharmacol Rev, 64, 706-21.   DOI
20 Siriwatanametanon N, Fiebich BL, Efferth T, et al (2010). Traditionally used Thai medicinal plants: in vitro antiinflammatory, anticancer and antioxidant activities. J Ethnopharmacol, 130, 196-207.   DOI
21 Stewart P, Boonsiri P, Puthong S, et al (2013). Antioxidant activity and ultrastructural changes in gastric cancer cell lines induced by Northeastern Thai edible folk plant extracts. BMC Complement Altern Med, 13, 60.   DOI
22 Sun C, Brown AJ, Jhingran A, et al (2014). Patient preferences for side effects associated with cervical cancer treatment. Int J Gynecol Cancer, 24, 1077-84.   DOI
23 Vidya PR, Senthil MR, Maitreyi S, et al (2010). The flavonoid quercetin induces cell cycle arrest and mitochondriamediated apoptosis in human cervical cancer (HeLa) cells through p53 induction and NF-kappaB inhibition. Eur J Pharmacol, 649, 84-91.   DOI   ScienceOn
24 Waiyaput W, Payungporn S, Issara-Amphorn J, et al (2012). Inhibitory effects of crude extracts from some edible Thai plants against replication of hepatitis B virus and human liver cancer cells. BMC Complement Altern Med, 12, 246.   DOI
25 Wilailak S (2009). Epidemiologic report of gynecologic cancer in Thailand. J Gynecol Oncol, 20, 81-3.   DOI
26 Xiong J, Liu XH, Bui VB, et al (2014). Phenolic constituents from the leaves of Cratoxylum formosum ssp. pruniflorum. Fitoterapia, 94, 114-9.   DOI
27 Xu JG, Hu QP, Liu Y (2012). Antioxidant and DNA-protective activities of chlorogenic acid Isomers. J Agric Food Chem, 60, 11625-30.   DOI
28 Zhao B, Hu M (2013). Gallic acid reduces cell viability, proliferation, invasion and angiogenesis in human cervical cancer cells. Oncol Lett, 6, 1749-55.
29 zur Hausen H (1999). Papillomaviruses in human cancers. Proc Assoc Am Physicians, 111, 581-7.   DOI