Cytotoxic effect and induction of apoptosis in human cervical cancer cells by a wood extract from Prosopis laevigata

References

• Arbyn, M., et al., 2020. Estimates of incidence and mortality of cervical cancer in 2018: a worldwide analysis. The Lancet Global Health, 8 (2), e191–e203.
   PubMed Web of Science ®Google Scholar
• Arias-González, I., et al., 2018. Cytotoxic effect of Kalanchoe flammea and induction of intrinsic mitochondrial apoptotic signaling in prostate cancer cells. Journal of Ethnopharmacology, 222, 133–147.
   PubMed Web of Science ®Google Scholar
• Asati, V., et al., 2021. Comparative analysis of antioxidant and antiproliferative activities of crude and purified flavonoid enriched fractions of pods/seeds of two desert legumes Prosopis cineraria and Cyamopsis tetragonoloba. Heliyon, 7 (6), e07304.
   PubMed Web of Science ®Google Scholar
• Azahar, N.H., et al., 2019. Mutagenic study of benzimidazole derivatives with (+S9) and without (-S9) metabolic activation. International Journal of Molecular Sciences, 20 (18), 4324.
   PubMed Web of Science ®Google Scholar
• Azqueta, A., and Collins, A., 2016. Polyphenols and DNA damage: a mixed blessing. Nutrients, 8 (12), 721–785.
   PubMed Web of Science ®Google Scholar
• Cardozo, M.L., et al., 2010. Evaluation of antioxidant capacity, genotoxicity and polyphenol content of non conventional foods: prosopis flour. Food Research International, 43 (5), 1505–1510.
   Web of Science ®Google Scholar
• Celegato, M., et al., 2020. A novel small-molecule inhibitor of the human papillomavirus E6-p53 interaction that reactivates p53 function and blocks cancer cells growth. Cancer Letters, 470, 115–125.
   PubMed Web of Science ®Google Scholar
• Chen, S.H., and Chang, J.Y., 2019. New insights into mechanisms of cisplatin resistance: from tumor cell to microenvironment. International Journal of Molecular Sciences, 20 (17), 4136.
   PubMed Web of Science ®Google Scholar
• Chen, W., et al., 2020. Phenolic compounds from Polygonum chinense induce growth inhibition and apoptosis of cervical cancer SiHa Cells. BioMed Research International, 2020, 1–8.
   Web of Science ®Google Scholar
• de Oliveira, P.F., et al., 2015. Cytotoxicity screening of essential oils in cancer cell lines. Revista Brasileira de Farmacognosia, 25 (2), 183–188.
   Google Scholar
• Ding, L., et al., 2020. The roles of cyclin-dependent kinases in cell-cycle progression and therapeutic strategies in human breast cancer. International Journal of Molecular Sciences, 21 (6), 1928–1960.
   PubMed Web of Science ®Google Scholar
• Elmore, S., 2007. Apoptosis: a review of programmed cell death Susan. Toxicologic Pathology, 35 (4), 495–516.
   PubMed Web of Science ®Google Scholar
• Espinosa-Paredes, D.A., et al., 2020. Echinacea angustifolia DC extract induces apoptosis and cell cycle arrest and synergizes with paclitaxel in the MDA-MB-231 and MCF-7 human breast cancer cell lines. Nutrition and Cancer, 73(11–12), 2287–2305.
   Web of Science ®Google Scholar
• European Medicines Agency. 2008. Guideline on the assessment of genotoxicity of herbal substances/preparations. London: Committee on Herbal Medicinal Products.
   Google Scholar
• FAO. 2001. Análisis de la informacion sobre productos forestales no madereros en Mexico. Chile: Santiago de Chile.
   Google Scholar
• Federico, C., et al., 2021. Localized delivery of cisplatin to cervical cancer improves its therapeutic efficacy and minimizes its side effect profile. International Journal of Radiation Oncology, Biology, Physics, 109 (5), 1483–1494.
   PubMed Web of Science ®Google Scholar
• Gardino, A.K., and Yaffe, M.B., 2011. 14-3-3 proteins as signaling integration points for cell cycle control and apoptosis. Seminars in Cell & Developmental Biology, 22 (7), 688–695.
   PubMed Web of Science ®Google Scholar
• Ghosh, S., 2019. Cisplatin: the first metal based anticancer drug. Bioorganic Chemistry, 88, 102925.
   PubMed Web of Science ®Google Scholar
• Hapon, M., et al., 2014. Aqueous extract of Prosopis strombulifera (LAM) BENTH induces cytotoxic effects against tumor cell lines without systemic alterations in BALB/c mice. Journal of Clinical Toxicology, 04 (06), 4–11.
   Google Scholar
• Herranz-López, M., Losada-Echeberría, M., and Barrajón-Catalán, E., 2018. The multitarget activity of natural extracts on cancer: synergy and xenohormesis. Medicines, 6 (1), 6.
   Google Scholar
• Hu, X.M., et al., 2021. Guidelines for regulated cell death assays: a systematic summary, a categorical comparison, a prospective. Frontiers in Cell and Developmental Biology, 9, 1–28.
   Web of Science ®Google Scholar
• Ibarra-Berumen, J., Rosales-Castro, M., and Ordaz-Pichardo, C., 2021. Potential use of wood metabolites for cancer treatment. Natural Product Research, 1–17.
   PubMed Web of Science ®Google Scholar
• Keene, M.R., et al., 2019. Complementary and alternative medicine use in cancer: a systematic review. Complementary Therapies in Clinical Practice, 35, 33–47.
   PubMed Web of Science ®Google Scholar
• Koch, W., 2019. Dietary polyphenols-important non-nutrients in the prevention of chronic noncommunicable diseases. A systematic review. Nutrients, 11 (5), 1035–1039.
   PubMed Web of Science ®Google Scholar
• Kumar, N., et al., 2019. Extrapolation of phenolic compounds as multi-target agents against cancer and inflammation. Journal of Biomolecular Structure & Dynamics, 37 (9), 2355–2369.
   PubMed Web of Science ®Google Scholar
• Kunnumakkara, A.B., et al., 2019. Cancer drug development: the missing links. Experimental Biology and Medicine, 244 (8), 663–689.
   Web of Science ®Google Scholar
• Lachance, J.C., et al., 2020. Targeting hallmarks of cancer with a food-system-based approach. Nutrition, 69, 110563.
   PubMed Web of Science ®Google Scholar
• Loeb, W., and Quimby, F., 1999. The clinical chemistry of laboratory animals. 2nd ed. Philadelphia: Taylor & Francis.
   Google Scholar
• Ma, L., et al., 2021. Plant natural products: promising resources for cancer chemoprevention. Molecules, 26 (4), 933.
   PubMed Web of Science ®Google Scholar
• Mahapatra, E., et al., 2021. Insights of cisplatin resistance in cervical cancer: a decision making for cellular survival. In: R. Rajkumar, ed. Cervical cancer – a global public health treatise. London: IntechOpen, 1–17.
   Google Scholar
• Manosroi, A., et al., 2015. Potent anti-proliferative effects against oral and cervical cancers of Thai medicinal plants selected from the Thai/Lanna medicinal plant recipe database ‘MANOSROI III’. Pharmaceutical Biology, 53 (7), 1075–1081.
   PubMed Web of Science ®Google Scholar
• Maron, D.M., and Ames, B.N., 1983. Revised methods for the Salmonella mutagenicity test. Mutation Research, 113 (3–4), 173–215.
   PubMed Web of Science ®Google Scholar
• Merecz-Sadowska, A., et al., 2021. Antioxidant properties of plant-derived phenolic compounds and their effect on skin fibroblast cells. Antioxidants, 10 (5), 724–726.
   Web of Science ®Google Scholar
• Mosmann, T., 1983. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. Journal of Immunological Methods, 65 (1–2), 55–63.
   PubMed Web of Science ®Google Scholar
• Naseri, M.H., et al., 2015. Up regulation of Bax and down regulation of Bcl2 during 3-NC mediated apoptosis in human cancer cells. Cancer Cell International, 15 (1), 1–9.
   PubMedGoogle Scholar
• National Cancer Institute (NCI). 2019. Cervical cancer treatment (PDQ®). In: PDQ cancer information summaries. (United States of America). Available from: https://www.ncbi.nlm.nih.gov/books/NBK66058/ [Accessed 5 May 2022].
   Google Scholar
• OECD. 2001. Test Guideline No. 423: Acute oral toxicity – acute toxic class method. https://www.oecd-ilibrary.org/environment/test-no-423-acute-oral-toxicity-acute-toxic-class-method_9789264071001-en
   Google Scholar
• OECD 2008. Test Guideline No. 407: Repeated dose 28-day oral toxicity study in rodents. https://www.oecd-ilibrary.org/environment/test-no-407-repeated-dose-28-day-oral-toxicity-study-in-rodents_9789264070684-en
   Google Scholar
• Padilla, L.A., Leung, B.S., and Carson, L.F., 2002. Evidence of an association between human papillomavirus and impaired chemotherapy-induced apoptosis in cervical cancer cells. Gynecologic Oncology, 85 (1), 59–66.
   PubMed Web of Science ®Google Scholar
• Persia, F.A., et al., 2020. UHPLC–Q/Orbitrap/MS/MS fingerprinting and antitumoral effects of Prosopis strombulifera (LAM.) BENTH. queous extract on allograft colorectal and melanoma cancer models. Heliyon, 6 (2), e03353.
   PubMed Web of Science ®Google Scholar
• Pezzani, R., et al., 2019. Synergistic effects of plant derivatives and conventional chemotherapeutic agents: an update on the cancer perspective. Medicina, 55 (4), 110.
   PubMedGoogle Scholar
• Porter, A.G., and Jänicke, R.U., 1999. Emerging roles of caspase-3 in apoptosis. Cell Death and Differentiation, 6 (2), 99–104.
   PubMed Web of Science ®Google Scholar
• Prabha, D.S., Dahms, H.U., and Malliga, P., 2012. Assessment of acute and subactue oral toxicity of ethanolic extracts of Prosopis juliflora on rattus norvegicus. Journal of Herbal Medicine and Toxicology, 6 (1), 61–65.
   Google Scholar
• Prakash, S., et al., 2020. Isolation of hesperetin – a flavonoid from Cordia sebestena flower extract through antioxidant assay guided method and its antibacterial, anticancer effect on cervical cancer via in vitro and in silico molecular docking studies. Journal of Molecular Structure, 1207, 127751.
   Web of Science ®Google Scholar
• Rai, Y., et al., 2018. Mitochondrial biogenesis and metabolic hyperactivation limits the application of MTT assay in the estimation of radiation induced growth inhibition. Scientific Reports, 8 (1), 1–15.
   PubMedGoogle Scholar
• Robertson, S., Narayanan, N., and Ravi Nargis, N.R., 2012. Toxicity evaluation on hydroalcoholic extract of leaf and stem bark of Prosopis cineraria. International Journal of Pharmacy and Pharmaceutical Sciences, 4 (3), 113–118.
   Google Scholar
• Rodríguez-Sauceda, E.N., et al., 2014. Análisis técnico del árbol del mezquite (Prosopis laevigata Humb. & Bonpl. ex Willd.) en México. Ra Ximhai, 10 (3), 173–194.
   Google Scholar
• Rogers, C., et al., 2017. Cleavage of DFNA5 by caspase-3 during apoptosis mediates progression to secondary necrotic/pyroptotic cell death. Nature Communications, 8 (1), 1–14.
   PubMedGoogle Scholar
• Rosales-Castro, M., et al., 2015. Antioxidant phenolic compounds of ethanolic and aqueous extracts from pink cedar (Acrocarpus fraxinifolius Whight & Arn.) Bark at Two Tree Ages. Journal of Wood Chemistry and Technology, 35 (4), 270–279.
   Web of Science ®Google Scholar
• Sevgi, K., Tepe, B., and Sarikurkcu, C., 2015. Antioxidant and DNA damage protection potentials of selected phenolic acids. Food and Chemical Toxicology, 77, 12–21.
   PubMed Web of Science ®Google Scholar
• Strasser, A., and Vaux, D.L., 2020. Cell death in the origin and treatment of cancer. Molecular Cell, 78 (6), 1045–1054.
   PubMed Web of Science ®Google Scholar
• Titlow, W.B., Lee, C., and Ryou, C., 2013. Characterization of toxicological properties of L-lysine polymers in CD-1 mice. Journal of Microbiology and Biotechnology, 23 (7), 1015–1022.
   PubMed Web of Science ®Google Scholar
• Ukande, M.D., et al., 2019. Review on pharmacological potentials of Prosopis juliflora. Journal of Drug Delivery and Therapeutics, 9 (4-s), 755–760.
   Google Scholar
• Utage, B.G., et al., 2018. Prosopis juliflora (Sw.), DC induces apoptosis and cell cycle arrest in triple negative breast cancer cells: in vitro and in vivo investigations. Oncotarget, 9 (54), 30304–30323.
   PubMedGoogle Scholar
• Ventura, E., and Giordano, A., 2019. Cell cycle. In: Reference module in life sciences. Elsevier.
   Google Scholar
• Villegas-Novoa, C., et al., 2019. Acetone effects on Buddleja scordioides polyphenol extraction process and assessment of their cellular antioxidant capacity and anti-inflammatory activity. Medicinal Chemistry Research, 28 (12), 2218–2231.
   Web of Science ®Google Scholar
• Wang, F., et al., 2016. Eriodictyol-induced anti-cancer and apoptotic effects in human hepatocellular carcinoma cells are associated with cell cycle arrest and modulation of apoptosis-related proteins. Bangladesh Journal of Pharmacology, 11 (2), 285–291.
   Web of Science ®Google Scholar
• WHO, 2018. Noncommunicable diseases. Available from: https://www.who.int/news-room/fact-sheets/detail/noncommunicable-diseases [Accessed 26 Jun 2019].
   Google Scholar
• Wode, K., et al., 2019. Cancer patients’ use of complementary and alternative medicine in Sweden: a cross-sectional study. BMC Complementary and Alternative Medicine, 19 (1), 1–11.
   PubMed Web of Science ®Google Scholar
• Yildizhan, H., et al., 2018. Treatment strategies in cancer from past to present. In: Drug targeting and stimuli sensitive drug delivery systems, 1–37.
   Google Scholar
• Zhang, Y., Zhang, R., and Ni, H., 2020. Eriodictyol exerts potent anticancer activity against A549 human lung cancer cell line by inducing mitochondrial-mediated apoptosis, G2/M cell cycle arrest and inhibition of m-TOR/PI3K/Akt signalling pathway. Archives of Medical Science, 16 (2), 446–452.
   PubMed Web of Science ®Google Scholar
• Zhao, W., et al., 2020. MicroRNA-154-5p regulates the HPV16 E7-pRb pathway in cervical carcinogenesis by targeting CUL2. Journal of Cancer, 11 (18), 5379–5389.
   PubMed Web of Science ®Google Scholar
• Zhong, J., et al., 2022. Current insights into phytochemistry, nutritional, and pharmacological properties of prosopis plants. Evidence-Based Complementary and Alternative Medicine, 2022, 1–18.
   Web of Science ®Google Scholar
• Zhou, J., Xia, L., and Zhang, Y., 2019. Naringin inhibits thyroid cancer cell proliferation and induces cell apoptosis through repressing PI3K/AKT pathway. Pathology, Research and Practice, 215 (12), 152707.
   PubMed Web of Science ®Google Scholar