References
- Sulaiman GM, Waheeb HM, Jabir MS, Khazaal SH, Dewir YH, Naidoo Y. Hesperidin loaded on gold nanoparticles as a drug delivery system for a successful biocompatible, anti-cancer, anti-inflammatory and phagocytosis inducer model. Sci Rep. 2020;10(1):1–16. doi:https://doi.org/10.1038/s41598-020-66419-6
- Casais-Molina M, Cab C, Canto G, Medina J, Tapia A. Carbon nanomaterials for breast cancer treatment. J Nanomater. 2018;2018:1–9. doi:https://doi.org/10.1155/2018/2058613
- Noori-Daloii M, Hesami S. Telomerase and it’s inhibition in caner: a review article. Tehran Univ Med J. 2009;67:599–607.
- Zelle SG, Baltussen RM. Economic analyses of breast cancer control in low- and middle-income countries: a systematic review. Syst Rev. 2013;2:20. doi:https://doi.org/10.1186/2046-4053-2-20
- Barabadi H, Mahjoub MA, Tajani B, Ahmadi A, Junejo Y, Saravanan M. Emerging theranostic biogenic silver nanomaterials for breast cancer: a systematic review. J Clust Sci. 2019;30(2):259–79. doi:https://doi.org/10.1007/s10876-018-01491-7
- Saeed N, Hamzah I, Mahmood S. The applications of nano-medicine in the breast cancer therapy. Bristol: IOP Publishing; 2021.
- Saravanan M, Vahidi H, Medina Cruz D, Vernet-Crua A, Mostafavi E, Stelmach R, Webster TJ, Mahjoub MA, Rashedi M, Barabadi H, et al. Emerging antineoplastic biogenic gold nanomaterials for breast cancer therapeutics: a systematic review. Int J Nanomedicine. 2020;15:3577–95. doi:https://doi.org/10.2147/IJN.S240293
- Ali SH, Sulaiman GM, Al-Halbosiy MM, Jabir MS, Hameed AH. Fabrication of hesperidin nanoparticles loaded by poly lactic co-Glycolic acid for improved therapeutic efficiency and cytotoxicity. Artif Cells Nanomed Biotechnol. 2019;47(1):378–94. doi:https://doi.org/10.1080/21691401.2018.1559175
- Barabadi H, Hosseini O, Damavandi Kamali K, Jazayeri Shoushtari F, Rashedi M, Haghi-Aminjan H, Saravanan M. Emerging theranostic silver nanomaterials to combat lung cancer: a systematic review. J Clust Sci. 2020;31(1):1–10. doi:https://doi.org/10.1007/s10876-019-01639-z
- Ramezanpour H, Setayeshi S, Akbari M. A novel scheme for optimal control of a nonlinear delay differential equations model to determine effective and optimal administrating chemotherapy agents in breast cancer. Iran J Cancer Prev. 2011;4(4):154–62.
- Takeda S, Hirayama A, Urata S, Mano N, Fukagawa K, Imamura M, Irii A, Kitajima S, Masuyama T, Nomiyama M, et al. Cannabidiol-2’,6’-dimethyl ether as an effective protector of 15-lipoxygenase-mediated low-density lipoprotein oxidation in vitro. Biol Pharm Bull. 2011;34(8):1252–6. doi:https://doi.org/10.1248/bpb.34.1252
- Afrin S, Giampieri F, Gasparrini M, Forbes-Hernández TY, Cianciosi D, et al. Dietary phytochemicals in colorectal cancer prevention and treatment: a focus on the molecular mechanisms involved. Biotechnol Adv. 2018;38:107322.
- Siddiqui JA, Singh A, Chagtoo M, Singh N, Godbole MM, Chakravarti B. Phytochemicals for breast cancer therapy: current status and future implications. Curr Cancer Drug Targets. 2015;15(2):116–35. doi:https://doi.org/10.2174/1568009615666141229152256
- Meybodi NM, Mortazavian AM, Monfared AB, Sohrabvandi S, Meybodi FA. Phytochemicals in cancer prevention: a review of the evidence. Iranian J Cancer Prev. 2017;10.
- Hosseini A, Ghorbani A. Cancer therapy with phytochemicals: evidence from clinical studies. Avicenna J Phytomed. 2015;5(2):84–97.
- Sadrnia M. Effects of aqueous extracts and essential oils of Mentha and Satureja on the Aflatoxin B1 production by Aspergillus flavus. J Arak Univ Med Sci. 2018;21:63–73.
- Badawi NM, Teaima MH, El-Say KM, Attia DA, El-Nabarawi MA, Elmazar MM. Pomegranate extract-loaded solid lipid nanoparticles: design, optimization, and in vitro cytotoxicity study. Int J Nanomedicine. 2018;13:1313–26. doi:https://doi.org/10.2147/IJN.S154033
- Saeidnia S, Gohari AR. Importance of Brassica napus as a medicinal food plant. J Med Plants Res. 2012;6:2700–3.
- Kumari P, Ghosh B, Biswas S. Nanocarriers for cancer-targeted drug delivery. J Drug Target. 2016;24(3):179–91. doi:https://doi.org/10.3109/1061186X.2015.1051049
- Barabadi H, Vahidi H, Kamali KD, Rashedi M, Saravanan M. Antineoplastic biogenic silver nanomaterials to combat cervical cancer: a novel approach in cancer therapeutics. J Clust Sci. 2020;31(4):659–72. doi:https://doi.org/10.1007/s10876-019-01697-3
- Sulaiman GM, Jabir MS, Hameed AH. Nanoscale modification of chrysin for improved of therapeutic efficiency and cytotoxicity. Artif Cells Nanomed Biotechnol. 2018;46(sup1):708–20. doi:https://doi.org/10.1080/21691401.2018.1434661
- Danhier F, Ansorena E, Silva JM, Coco R, Le Breton A, Préat V. PLGA-based nanoparticles: an overview of biomedical applications. J Control Release. 2012;161(2):505–22. doi:https://doi.org/10.1016/j.jconrel.2012.01.043
- Baban DF, Seymour LW. Control of tumour vascular permeability. Adv Drug Deliv Rev. 1998;34(1):109–19. doi:https://doi.org/10.1016/s0169-409x(98)00003-9
- Maeda H. The enhanced permeability and retention (EPR) effect in tumor vasculature: the key role of tumor-selective macromolecular drug targeting. Adv Enzyme Regul. 2001;41:189–207. doi:https://doi.org/10.1016/s0065-2571(00)00013-3
- Aggarwal V, Tuli H, Varol A, Thakral F, Yerer M, Sak K, Varol M, Jain A, Khan M, Sethi G, et al. Role of reactive oxygen species in cancer progression: Molecular mechanisms and recent advancements. Biomolecules. 2019;9(11):735. doi:https://doi.org/10.3390/biom9110735
- Pastor DM, Irby RB, Poritz LS. Tumor Necrosis Factor alpha induces p53 up-regulated modulator of apoptosis expression in colorectal cancer cell lines. Dis Colon Rectum. 2010;53(3):257–63. doi:https://doi.org/10.1007/DCR.0b013e3181c522c7
- Li Y-L, Zhao H, Ren X-B. Relationship of VEGF/VEGFR with immune and cancer cells: staggering or forward? Cancer Biol Med. 2016;13(2):206–14. doi:https://doi.org/10.20892/j.issn.2095-3941.2015.0070
- Devarajan E, Sahin AA, Chen JS, Krishnamurthy RR, Aggarwal N, Brun A-M, Sapino A, Zhang F, Sharma D, Yang X-H, et al. Down-regulation of caspase 3 in breast cancer: a possible mechanism for chemoresistance. Oncogene. 2002;21(57):8843–51. doi:https://doi.org/10.1038/sj.onc.1206044
- Pistritto G, Trisciuoglio D, Ceci C, Garufi A, D’Orazi G. Apoptosis as anticancer mechanism: function and dysfunction of its modulators and targeted therapeutic strategies. Aging (Albany, NY). 2016;8(4):603–19. doi:https://doi.org/10.18632/aging.100934
- Sznarkowska A, Kostecka A, Meller K, Bielawski KP. Inhibition of cancer antioxidant defense by natural compounds. Oncotarget. 2017;8(9):15996–6016. doi:https://doi.org/10.18632/oncotarget.13723
- Rajasekar J, Perumal MK, Vallikannan B. A critical review on anti-angiogenic property of phytochemicals. J Nutr Biochem. 2019;71:1–15. doi:https://doi.org/10.1016/j.jnutbio.2019.04.006
- Brentnall M, Rodriguez-Menocal L, De Guevara RL, Cepero E, Boise LH. Caspase-9, caspase-3 and caspase-7 have distinct roles during intrinsic apoptosis. BMC Cell Biol. 2013;14:32. doi:https://doi.org/10.1186/1471-2121-14-32
- Aubrey BJ, Kelly GL, Janic A, Herold MJ, Strasser A. How does p53 induce apoptosis and how does this relate to p53-mediated tumour suppression? Cell Death Differ. 2018;25(1):104–13. doi:https://doi.org/10.1038/cdd.2017.169
- Kearney CJ, Cullen SP, Tynan GA, Henry CM, Clancy D, Lavelle EC, Martin SJ. Necroptosis suppresses inflammation via termination of TNF- or LPS-induced cytokine and chemokine production. Cell Death Differ. 2015;22(8):1313–27. doi:https://doi.org/10.1038/cdd.2014.222
- Hajebi S, Tabrizi MH, Moghaddam MN, Shahraki F, Yadamani S. Rapeseed flower pollen bio-green synthesized silver nanoparticles: A promising antioxidant, anticancer and antiangiogenic compound. J Biol Inorg Chem. 2019;24(3):395–404. doi:https://doi.org/10.1007/s00775-019-01655-4
- Hafezi Ghahestani Z, Alebooye Langroodi F, Mokhtarzadeh A, Ramezani M, Hashemi M. Evaluation of anti-cancer activity of PLGA nanoparticles containing crocetin. Artif Cells Nanomed Biotechnol. 2017;45(5):955–60. doi:https://doi.org/10.1080/21691401.2016.1198359
- Latif S, Diosady LL, Anwar F. Enzyme‐assisted aqueous extraction of oil and protein from canola (Brassica napus L.) seeds. Eur J Lipid Sci Technol. 2008;110(10):887–92. doi:https://doi.org/10.1002/ejlt.200700319
- Albukhaty S, Al-Musawi S, Abdul Mahdi S, Sulaiman GM, Alwahibi MS, Dewir YH, Soliman DA, Rizwana H. Investigation of dextran-coated superparamagnetic nanoparticles for targeted vinblastine controlled release, delivery, apoptosis induction, and gene expression in pancreatic cancer cells. Molecules. 2020;25(20):4721. doi:https://doi.org/10.3390/molecules25204721
- Soltani M, Parivar K, Baharara J, Kerachian MA, Asili J. Putative mechanism for apoptosis-inducing properties of crude saponin isolated from sea cucumber (Holothuria leucospilota) as an antioxidant compound. Iran J Basic Med Sci. 2015;18(2):180–7.
- Honary S, Barabadi H, Ebrahimi P, Naghibi F, Alizadeh A. Development and optimization of biometal nanoparticles by using mathematical methodology: a microbial approach. Zurich: Trans Tech Publ; 2015.
- Stetefeld J, McKenna SA, Patel TR. Dynamic light scattering: a practical guide and applications in biomedical sciences. Biophys Rev. 2016;8(4):409–27. doi:https://doi.org/10.1007/s12551-016-0218-6
- Barabadi H, Honary S, Ebrahimi P, Alizadeh A, Naghibi F, Saravanan M. Optimization of myco-synthesized silver nanoparticles by response surface methodology employing Box-Behnken design. Inorganic and Nano-Metal Chem. 2019;49(2):33–43. doi:https://doi.org/10.1080/24701556.2019.1583251
- Salopek B, Krasic D, Filipovic S. Measurement and application of zeta-potential. Rudarsko-Geolosko-Naftni Zbornik. 1992;4:147.
- Bansal P, Gupta VV, Bansal R, Sapra R. Dietary phytochemicals in cell cycle arrest and apoptosis-an insight. J Drug Delivery Ther. 2012;2(2):8–17. doi:https://doi.org/10.22270/jddt.v2i2.121
- Mukerjee A, Vishwanatha JK. Formulation, characterization and evaluation of curcumin-loaded PLGA nanospheres for cancer therapy. Anticancer Res. 2009;29(10):3867–75.
- Zarogoulidis P, Cheva A, Zarampouka K, Huang H, Li C, Huang Y, Katsikogiannis N, Zarogoulidis K. Tocopherols and tocotrienols as anticancer treatment for lung cancer: future nutrition. J Thorac Dis. 2013;5(3):349–52.
- Soundararajan P, Kim JS. Anti-carcinogenic glucosinolates in cruciferous vegetables and their antagonistic effects on prevention of cancers. Molecules. 2018;23(11):2983. doi:https://doi.org/10.3390/molecules23112983
- Anantharaju PG, Gowda PC, Vimalambike MG, Madhunapantula SV. An overview on the role of dietary phenolics for the treatment of cancers. Nutr J. 2016;15(1):99. doi:https://doi.org/10.1186/s12937-016-0217-2
- Elrayess RA, El-Hak HNG. Anticancer Natural Products: A Review. Cancer Stud Mol Med Open J. 2019;5(1):11–25. doi:https://doi.org/10.17140/CSMMOJ-5-127
- Mutha RE, Surana SJ. Ultrasonic frequency based development of chrysin nanoparticles: assessment of bioavailability, anti-cancer activity and stability. Mater Technol. 2018;33(7):495–505. doi:https://doi.org/10.1080/10667857.2018.1464240
- Hamidi M, Azadi A, Rafiei P, Ashrafi H. A pharmacokinetic overview of nanotechnology-based drug delivery systems: an ADME-oriented approach. Critical Rev Therap Drug Carrier Syst. 2013;30:435–467.
- Khshemat V, Homayouni-Tabrizi M, Neamati A, Khadem F, Irani M. Fabrication, characterisation, and biological properties of chitosan nanoparticles containing Rapeseed Pollen Extract (RPE) on the MCF-7 Cell Line. Mater Technol. 2021:1–11. doi:https://doi.org/10.1080/10667857.2021.1921099
- Ashna M, Es-Haghi A, Karimi Noghondar M, Al Amara D, Yazdi MET. Greener synthesis of cerium oxide nanoemulsion using pollen grains of Brassica napus and evaluation of its antitumour and cytotoxicity properties. Mater Technol. 2020:1–8. doi:https://doi.org/10.1080/10667857.2020.1863558
- Shahraki F, Tabrizi MH, Moghaddam MN, Hajebi S. Bio-green synthesis ZnO-NPs in Brassica napus pollen extract: biosynthesis, antioxidant, cytotoxicity and pro-apoptotic properties. IET Nanobiotechnol. 2019;13(5):471–6. doi:https://doi.org/10.1049/iet-nbt.2018.5164
- Shabestarian H, Homayouni Tabrizi M, Movahedi M, Neamati A, Sharifnia F. Putative mechanism for cancer suppression by PLGA nanoparticles loaded with Peganum harmala smoke extract. J Microencapsulation. 2021;38(5):324. doi:https://doi.org/10.1080/02652048.2021.1917715
- Mohan LJ, McDonald L, Daly JS, Ramtoola Z. Optimising PLGA-PEG nanoparticle size and distribution for enhanced drug targeting to the inflamed intestinal barrier. Pharmaceutics. 2020;12(11):1114. doi:https://doi.org/10.3390/pharmaceutics12111114
- Teng X, Degterev A, Jagtap P, Xing X, Choi S, Denu R, Yuan J, Cuny GD . Structure-activity relationship study of novel necroptosis inhibitors. Bioorg Med Chem Lett. 2005;15(22):5039–44. doi:https://doi.org/10.1016/j.bmcl.2005.07.077
- Tait SW, Green DR. Caspase-independent cell death: leaving the set without the final cut. Oncogene. 2008;27(50):6452–61. doi:https://doi.org/10.1038/onc.2008.311
- Dhuriya YK, Sharma D. Necroptosis: a regulated inflammatory mode of cell death. J Neuroinflammation. 2018;15(1):199. doi:https://doi.org/10.1186/s12974-018-1235-0
- Essmann F, Engels IH, Totzke G, Schulze-Osthoff K, Jänicke RU. Apoptosis resistance of MCF-7 breast carcinoma cells to ionizing radiation is independent of p53 and cell cycle control but caused by the lack of caspase-3 and a caffeine-inhibitable event. Cancer Res. 2004;64(19):7065–72. doi:https://doi.org/10.1158/0008-5472.CAN-04-1082
- Laukens B, Jennewein C, Schenk B, Vanlangenakker N, Schier A, Cristofanon S, Zobel K, Deshayes K, Vucic D, Jeremias I, et al . Smac mimetic bypasses apoptosis resistance in FADD- or caspase-8-deficient cells by priming for tumor necrosis factor α-induced necroptosis. Neoplasia. 2011;13(10):971–IN29. doi:https://doi.org/10.1593/neo.11610
- Galluzzi L, Berghe TV, Vanlangenakker N, Buettner S, Eisenberg T, et al. Programmed necrosis: from molecules to health and disease. In: International review of cell and molecular biology. Amsterdam: Elsevier; 2011. pp. 1–35.
- Paul S, Bhattacharyya SS, Boujedaini N, Khuda-Bukhsh AR. Anticancer potentials of root extract of Polygala senega and its PLGA nanoparticles-encapsulated form. Evidence-Based Compl Alternat Med. 2010;2011:1–13.
- Azandeh SS, Abbaspour M, Khodadadi A, Khorsandi L, Orazizadeh M, Heidari-Moghadam A. Anticancer activity of curcumin-loaded PLGA nanoparticles on PC3 prostate cancer cells. Iran J Pharm Res. 2017;16(3):868–79.
- Nair KL, Thulasidasan AKT, Deepa G, Anto RJ, Kumar GV. Purely aqueous PLGA nanoparticulate formulations of curcumin exhibit enhanced anticancer activity with dependence on the combination of the carrier. Int J Pharm. 2012;425(1–2):44–52. doi:https://doi.org/10.1016/j.ijpharm.2012.01.003