The potential of ethanolic extract of Moringa oleifera leaves on HSF1 expression in oral cancer induced by benzo[a]pyrene
Downloads
Background: Oral cancer is the sixth most common malignancy that occurs in the world, with more than 330,000 deaths a year. In cancer, mutations occur in proteins, accompanied by unfolding proteins, caused by the unstable micro-environment in cells. To stabilise this condition, protein protectors called heat shock proteins (HSPs) are needed. HSPs are activated by a group of transcription factors known as heatshock factor 1 (HSF1). HSF1 is a considered target in cancer therapy. Moringa oleifera leaves are known to have anti-cancer properties because of bioactive compounds called flavonoid and isothiocyanate and are used as herbal therapy for cancer. Purpose: To investigate the potential effect of ethanolic extract of Moringa oleifera on HSF1 expression in oral cancer induced by benzo[a]pyrene. Methods: This study used 25 male Wistar ratsdivided into five groups consisting of the negative control group (K-), which was only given aquadest; the positive control group (K+), which was induced with benzo[a]pyrene and given aquadest; and treatment groups that were induced with benzo[a]pyrene and given Moringa oleifera leaf extract at concentrations of 3.125% (P1), 6.25% (P2), and 9.375% (P3). Examination of HSF1 expression was carried out by immunohistochemistry staining. Data were analysed using the Kruskal–Wallis test and post-hoc Tukey HSD. Results: HSF1 expression in the P1, P2, and P3 groups decreased significantly compared to the K+ group. There were no significant differences between the P1, P2, and P3 groups (p > 0.005). Conclusion: Ethanolic extract of Moringa oleifera leaves in three concentrations can decrease expression of HSF1 in oral cancer induced by benzo[a]pyrene.
Downloads
Li D, Yallowitz A, Ozog L, Marchenko N. A gain-of-function mutant p53-HSF1 feed forward circuit governs adaptation of cancer cells to proteotoxic stress. Cell Death Dis. 2014; 5(4): 1–11.
Dai C, Sampson SB. HSF1: Guardian of proteostasis in cancer. Trends Cell Biol. 2016; 26(1): 17–28.
Chatterjee S, Burns TF. Targeting heat shock proteins in cancer: a promising therapeutic approach. Int J Mol Sci. 2017; 18(9): 1–39.
Nagai N, Nakai A, Nagata K. Quercetin suppresses heat shock response by down regulation of HSF1. Biochem Biophys Res Commun. 1995; 208(3): 1099–105.
Yang W, Cui M, Lee J, Gong W, Wang S, Fu J, Wu G, Yan K. Heat shock protein inhibitor, quercetin, as a novel adjuvant agent to improve radiofrequency ablation-induced tumor destruction and its molecular mechanism. Chinese J Cancer Res. 2016; 28(1): 19–28.
Sarkars R, Mukherjee S, Roy M. Targeting heat shock proteins by phenethyl isothiocyanate results in cell-cycle arrest and apoptosis of human breast cancer cells. Nutr Cancer. 2013; 65(3): 480–93.
Huang SH, O'Sullivan B. Oral cancer: current role of radiotherapy and chemotherapy. Med Oral Patol Oral Cir Bucal. 2013; 18(2): e233–40.
Pearce A, Haas M, Viney R, Pearson SA, Haywood P, Brown C, Ward R. Incidence and severity of self-reported chemotherapy side effects in routine care: a prospective cohort study. PLoS One. 2017; 12(10): 1–12.
Kolokythas A. Long-term surgical complications in the oral cancer patient: a comprehensive review. Part I. J Oral Maxillofac Res. 2010; 1(3): 1–10.
Leone A, Spada A, Battezzati A, Schiraldi A, Aristil J, Bertoli S. Cultivation, genetic, ethnopharmacology, phytochemistry and pharmacology of Moringa oleifera leaves: an overview. Int J Mol Sci. 2015; 16(6): 12791–835.
Gopalakrishnan L, Doriya K, Kumar DS. Moringa oleifera: a review on nutritive importance and its medicinal application. Food Sci Hum Wellness. 2016; 5(2): 49–56.
Budhy TI, Istiati, Sumaryono B, Arundia I, Khrisnanthi RS. Hedyotiscorymbosa (L.) Lamk - The potential inhibitor extract of oral cancer cell progressivity in benzopyrene induced rattus novergicus. J Int Dent Med Res. 2018; 11(1): 312–7.
Thalia A. Potensi ekstrak daun kelor (Moringa oliefera) terhadap ekspresi Ki-67 pada sel kanker rongga mulut tikus Wistar. Thesis. Surabaya: Universitas Indonesia; 2018. p. 33.
Neville BW, Damm DD, Allen CM, Chi AC. Oral and maxillofacial pathology. 4th ed. St. Louis: Saunders; 2015. p. 286–7.
Voisine C, Orton K, Morimoto RI. Protein misfolding, chaperone networks, and the heat shock response in the nervous system. In: Molecular Neurology. Elsevier; 2007. p. 59–76.
Kim JY, Yenari M. Heat shock proteins and the stress response. In: Primer on cerebrovascular diseases. 2nd ed. Elsevier; 2017. p. 273–5.
Wang Q, Zhang YC, Zhu LF, Pan L, Yu M, Shen WL, Li B, Zhang W, Liu LK. Heat shock factor 1 in cancer-associated fibroblasts is a potential prognostic factor and drives progression of oral squamous cell carcinoma. Cancer Sci. 2019; 110(5): 1790–803.
Dayalan Naidu S, Suzuki T, Yamamoto M, Fahey JW, Dinkova-Kostova AT. Phenethyl Isothiocyanate, a dual activator of transcription factors NRF2 and HSF1. Mol Nutr Food Res. 2018; 62(18): 1–9.
Chen Z, Forman LW, Williams RM, Faller D V. Protein kinase C-delta inactivation inhibits the proliferation and survival of cancer stem cells in culture and in vivo. BMC Cancer. 2014; 14: 1–15.
Nararya SA. Uji toksisitas daun kelor (Moringa Oleifera) terhadap sel fibroblas gingiva menggunakan uji MTT assay. Thesis. Surabaya: Universitas Airlangga; 2018. p. 41–45.
- Every manuscript submitted to must observe the policy and terms set by the Dental Journal (Majalah Kedokteran Gigi).
- Publication rights to manuscript content published by the Dental Journal (Majalah Kedokteran Gigi) is owned by the journal with the consent and approval of the author(s) concerned.
- Full texts of electronically published manuscripts can be accessed free of charge and used according to the license shown below.
- The Dental Journal (Majalah Kedokteran Gigi) is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License