| تعداد نشریات | 31 |
| تعداد شمارهها | 834 |
| تعداد مقالات | 8,015 |
| تعداد مشاهده مقاله | 14,852,482 |
| تعداد دریافت فایل اصل مقاله | 9,586,507 |
Effect of Zinc Oxide Nanoparticles Conjugated with Safranal on MMP1 and mTOR Gene Expression in MCF-7 Breast Cancer Cells | ||
| Journal of Epigenetics | ||
| مقاله 2، دوره 6، شماره 2، بهمن 2025، صفحه 27-38 اصل مقاله (748.46 K) | ||
| نوع مقاله: Original Article | ||
| شناسه دیجیتال (DOI): 10.22111/jep.2025.52363.1092 | ||
| نویسندگان | ||
| Reihanneh Jassemnejad1؛ Amir Jalali* 2؛ Seyed Ataollah Sadat Shandiz3؛ Ali Salehzadeh4؛ Leila Kohan1 | ||
| 1Department of Biology, Ars. C., Islamic Azad University, Arsanjan, Iran. | ||
| 2Department of Biology, Faculty of Science, Arak University, Arak, Iran. | ||
| 3Department of Biology, CT. C., Islamic Azad University, Tehran, Iran. | ||
| 4Department of Biology, Ra. C., Islamic Azad University, Rasht, Iran. | ||
| چکیده | ||
| Breast cancer is a leading cause of cancer-related mortality worldwide. Recent studies suggest that nanoparticles can enhance therapeutic efficacy. This research investigates the effects of zinc oxide nanoparticles (ZnO NPs) conjugated with Safranal on the expression of key genes associated with metabolism in Michigan Cancer Foundation (MCF-7) breast cancer cell lines. ZnO@Glu-Safranal NPs were synthesized and characterized using FE-SEM, transmission electron microscope (TEM), FT-IR, XRD, and Zeta potential analysis. To assess the effects of ZnO@Glu-Safranal NPs on the expression of MMP1 and mTOR genes, the MCF-7 cell line was treated with the IC50 concentration of the nanoparticles (165 μg/mL) for 24 hours, while untreated cells were used as a control. Changes in gene expression levels were quantified using real-time PCR, and p ˂ 0.05 was considered statistically significant. The results showed decreased expression of MMP1 (0.87-fold, p = 0.02) and mTOR (0.86-fold, p = 0.03) in MCF-7 cell lines compared to the control group. The study demonstrates that ZnO@Glu-Safranal NPs effectively modulate the expression of key metabolic genes expression in breast cancer cell lines. These findings highlight their potential as an effective therapeutic strategy, emphasizing the need for further research into their mechanisms and clinical applications to enhance breast cancer treatment outcomes. | ||
| کلیدواژهها | ||
| Breast Neoplasms؛ Gene Expression؛ Nanoparticles؛ Safranal؛ Zinc Oxide | ||
| مراجع | ||
|
Abdalla, Y., Abdalla, A., Hamza, A.A., Amin, A., 2022. Safranal Prevents Liver Cancer Through Inhibiting Oxidative Stress and Alleviating Inflammation. Front. Pharmacol. 12, 777500. https://doi.org/10.3389/fphar.2021.777500
Ahamed, M., Akhtar, M.J., Raja, M., Ahmad, I., Siddiqui, M.K., AlSalhi, M.S., Alrokayan, S., 2011. ZnO nanorod-induced apoptosis in human alveolar adenocarcinoma cells via p53, survivin and bax/bcl-2 pathways: role of oxidative stress. Nanomedicine 7(6), 904–913. https://doi.org/10.1016/j.nano.2011.04.011
Al-Thani, A.N., Jan, A.G., Abbas, M., Geetha, M., Sadasivuni, K.K., 2024. Nanoparticles in cancer theragnostic and drug delivery: A comprehensive review. Life Sci. 352, 122899. https://doi.org/10.1016/j.lfs.2024.122899
Ambalavanan, N., Stanishevsky, A., Bulger, A., Halloran, B., Steele, C., Vohra, Y., Matalon, S., 2013. Effect of nanoparticles on lung inflammation. Am. J. Physiol. Lung Cell Mol. Physiol. 304, L152. https://doi.org/10.1152/ajplung.00013.2012
Anjum, S., Hashim, M., Malik, S.A., Khan, M., Lorenzo, J.M., Abbasi, B.H., Hano, C., 2021. Recent Advances in Zinc Oxide Nanoparticles (ZnO NPs) for Cancer Diagnosis, Target Drug Delivery, and Treatment. Cancers 13(18), 4570. https://doi.org/10.3390/cancers13184570
Annangi, B., Bach, J., Vales, G., Rubio, L., Marcos, R., Hernández, A., 2015. Long-term exposures to low doses of cobalt nanoparticles induce cell transformation enhanced by oxidative damage. Nanotoxicology 9(2), 138-147. https://doi.org/10.3109/17435390.2014.900582
Armand, L., Dagouassat, M., Belade, E., Simon-Deckers, A., Le Gouvello, S., Tharabat, C., Duprez, C., Andujar, P., Pairon, J.C., Boczkowski, J., Lanone, S., 2013. Titanium dioxide nanoparticles induce matrix metalloprotease 1 in human pulmonary fibroblasts partly via an interleukin-1β-dependent mechanism. Am. J. Respir. Cell Mol. Biol. 48(3), 354-363. https://doi.org/10.1165/rcmb.2012-0099OC
Bai, D.P., Zhang, X.F., Zhang, G.L., Huang, Y.F., Gurunathan, S., 2017. Zinc oxide nanoparticles induce apoptosis and autophagy in human ovarian cancer cells. Int. J. Nanomed. 12, 6521–6535. https://doi.org/10.2147/IJN.S140071
Blum, J.L., Rosenblum, L.K., Grunig, G., Beasley, M.B., Xiong, J.Q., Zelikoff, J.T., 2014. Inhalation toxicity of nanoparticles in lung tissue. Inhal. Toxicol. 26, 48. https://doi.org/10.3109/08958378.2013.851746
Edelmann, M.J., Shack, L.A., Naske, C.D., Walters, K.B., Nanduri, B., 2014. Proteomic analysis of cellular responses to nanoparticles. PLoS One 9, e114390. https://doi.org/10.1371/journal.pone.0114390
Ezhuthupurakkal, P.B., Ariraman, S., Arumugam, S., Subramaniyan, N., Muthuvel, S.K., Kumpati, P., Rajamani, B., Chinnasamy, T., 2018. Anticancer potential of ZnO nanoparticle-ferulic acid conjugate on Huh-7 and HepG2 cells and diethyl nitrosamine induced hepatocellular cancer on Wistar albino rat. Nanomedicine 14(2), 415–428. https://doi.org/10.1016/j.nano.2017.11.003
Franková, J., Pivodová, V., Vágnerová, H., Juráňová, J., Ulrichová, J., 2016. Effects of silver nanoparticles on primary cell cultures of fibroblasts and keratinocytes in a wound-healing model. J. Appl. Biomater. Funct. Mater. 14(2), e137–e142. https://doi.org/10.5301/jabfm.5000268
George, B.P., Rajendran, N.K., Houreld, N.N., Abrahamse, H., 2022. Rubus capped zinc oxide nanoparticles induce apoptosis in MCF-7 breast cancer cells. Molecules 27(20), 6862. https://doi.org/10.3390/molecules27206862
Gonzalez-Avila, G., Sommer, B., García-Hernandez, A.A., Ramos, C., Flores-Soto, E., 2022. Nanotechnology and matrix metalloproteinases in cancer diagnosis and treatment. Front. Mol. Biosci. 9, 918789. https://doi.org/10.3389/fmolb.2022.918789
Hashimoto, M., Yamaguchi, S., Sasaki, J., Kawai, K., Kawakami, H., Iwasaki, Y., Imazato, S., 2016. Inhibition of matrix metalloproteinases and toxicity of gold and platinum nanoparticles in L929 fibroblast cells. Eur. J. Oral Sci. 124(1), 68–74. https://doi.org/10.1111/eos.12235
Hua, H., Kong, Q., Zhang, H., Wang, J., Luo, T., Jiang, Y., 2019. Regulation of tumor biology by signaling pathways. J. Hematol. Oncol. 12, 71. https://doi.org/10.1186/s13045-019-0754-1
Kang, S.G., Zhou, G., Yang, P., Liu, Y., Sun, B., Huynh, T., Meng, H., Zhao, L., Xing, G., Chen, C., Zhao, Y., Zhou, R., 2012. Computational study of nanoparticle interactions. Proc. Natl. Acad. Sci. USA 109, 15431. https://doi.org/10.1073/pnas.1204600109
Khan, M.I., Mohammad, A., Patil, G., Naqvi, S.A., Chauhan, L.K., Ahmad, I., 2012. Toxicity evaluation of biomaterials. Biomaterials 33, 1477. https://doi.org/10.1016/j.biomaterials.2011.10.080
Li, Z., Guo, D., Yin, X., Ding, S., Shen, M., Zhang, R., Wang, Y., Xu, R., 2020. Zinc oxide nanoparticles induce human multiple myeloma cell death via reactive oxygen species and Cyt-C/Apaf-1/Caspase-9/Caspase-3 signaling pathway in vitro. Biomed. Pharmacother. 122, 109712. https://doi.org/10.1016/j.biopha.2019.109712
Liu, J., Li, H.Q., Zhou, F.X., Yu, J.W., Sun, L., Han, Z.H., 2017. Targeting the mTOR pathway in breast cancer. Tumour Biol. 39(6), 1010428317710825. https://doi.org/10.1177/1010428317710825
Liu, Y., Yu, H., Zhang, X., Wang, Y., Song, Z., Zhao, J., Shi, H., Li, R., Wang, Y., Zhang, L.W., 2018. Evaluation of nanoparticle safety in biological systems. Nanotoxicology 12, 586. https://doi.org/10.1080/17435390.2018.1466932
Liu, Z., Wu, Y., Guo, Z., Liu, Y., Shen, Y., Zhou, P., Lu, X., 2014. Effects of internalized gold nanoparticles with respect to cytotoxicity and invasion activity in lung cancer cells. PLoS One 9(6), e99175. https://doi.org/10.1371/journal.pone.0099175
Lunova, M., Smolková, B., Lynnyk, A., Uzhytchak, M., Jirsa, J., Kubinová, Š., Dejneka, A., Lunov, O., 2019. Nanoparticle-mediated cancer therapies. Cancers 11, 82. https://doi.org/10.3390/cancers11010082
Malaekeh-Nikouei, B., Mousavi, S.H., Shahsavand, S., Mehri, S., Nassirli, H., Moallem, S.A., 2013. Assessment of cytotoxic properties of safranal and nanoliposomal safranal in various cancer cell lines. Phytother. Res. 27(12), 1868–1873. https://doi.org/10.1002/ptr.4945
Medhat, A., Mansour, S., El-Sonbaty, S., Kandil, E., Mahmoud, M., 2017. Role of nanoparticles in tumor biology. Tumour Biol. 39, 1010428317717259. https://doi.org/10.1177/1010428317717259
Mishra, P., Ahmad, A., Al-Keridis, L.A., Alshammari, N., Alabdallah, N.M., Muzammil, K., Saeed, M., Ansari, I.A., 2022. Doxorubicin-Conjugated Zinc Oxide Nanoparticles, Biogenically Synthesised Using a Fungus Aspergillus niger, Exhibit High Therapeutic Efficacy against Lung Cancer Cells. Molecules 27(8), 2590. https://doi.org/10.3390/molecules27082590
Mishra, P., Ahmad, M.F.A., Al-Keridis, L.A., Saeed, M., Alshammari, N., Alabdallah, N.M., Tiwari, R.K., Ahmad, A., Verma, M., Fatima, S., Ansari, I.A., 2024. Corrigendum: Methotrexate-conjugated zinc oxide nanoparticles exert substantially improved cytotoxic effect on lung cancer cells by inducing apoptosis. Front. Pharmacol. 15, 1423402. https://doi.org/10.3389/fphar.2024.1423402
Mohamed, S.Y., Elshoky, H.A., El-Sayed, N.M., Fahmy, H.M., Ali, M.A., 2024. Ameliorative effect of zinc oxide-chitosan conjugates on the anticancer activity of cisplatin: Approach for breast cancer treatment. Int. J. Biol. Macromol. 257(Pt 1), 128597. https://doi.org/10.1016/j.ijbiomac.2023.128597
Morimoto, Y., Oyabu, T., Ogami, A., Myojo, T., Kuroda, E., Hirohashi, M., Shimada, M., Lenggoro, W., Okuyama, K., Tanaka, I., 2011. Safety assessment of nanoparticles in occupational environments. Ind. Health 49, 344. https://doi.org/10.2486/indhealth.MS1218
Mozdoori, N., Safarian, S., Sheibani, N., 2017. Augmentation of the cytotoxic effects of zinc oxide nanoparticles by MTCP conjugation: Non-canonical apoptosis and autophagy induction in human adenocarcinoma breast cancer cell lines. Mater. Sci. Eng. C 78, 949–959. https://doi.org/10.1016/j.msec.2017.03.300
Naghshineh, A., Dadras, A., Ghalandari, B., Riazi, G.H., Modaresi, S.M., Afrasiabi, A., Aslani, M.K., 2015. Safranal as a novel anti-tubulin binding agent with potential use in cancer therapy: An in vitro study. Chem.-Biol. Interact. 238, 151–160. https://doi.org/10.1016/j.cbi.2015.06.023
Opris, R., Tatomir, C., Olteanu, D., Moldovan, R., Moldovan, B., David, L., Nagy, A., Decea, N., Kiss, M.L., Filip, G.A., 2017. Effects of nanostructured materials on cellular response. Colloids Surf. B Biointerfaces 150, 192. https://doi.org/10.1016/j.colsurfb.2016.11.033
Park, E.J., Kim, H., Kim, Y., Park, K., 2010a. Intratracheal instillation of platinum nanoparticles may induce inflammatory responses in mice. Arch. Pharm. Res. 33(5), 727-735. https://doi.org/10.1007/s12272-010-0512-y
Park, E.J., Kim, H., Kim, Y., Yi, J., Choi, K., Park, K., 2010b. Inflammatory responses may be induced by a single intratracheal instillation of iron nanoparticles in mice. Toxicology 275(1-3), 65-71. https://doi.org/10.1016/j.tox.2010.06.002
Pascarelli, N.A., Moretti, E., Terzuoli, G., Lamboglia, A., Renieri, T., Fioravanti, A., Collodel, G., 2013. Effects of gold and silver nanoparticles in cultured human osteoarthritic chondrocytes. J. Appl. Toxicol. 33(12), 1506-1513. https://doi.org/10.1002/jat.2912
Puente, X.S., Sánchez, L.M., Overall, C.M., López-Otín, C., 2003. Human and mouse proteases: a comparative genomic approach. Nat. Rev. Genet. 4, 544–558. https://doi.org/10.1038/nrg1111
Roy, R., Singh, S.K., Chauhan, L.K., Das, M., Tripathi, A., Dwivedi, P.D., 2014. Cellular response to toxic nanoparticles. Toxicol. Lett. 227, 29. https://doi.org/10.1016/j.toxlet.2014.02.024
Rudolph, A., Chang-Claude, J., Schmidt, M.K., 2016. Gene-environment interaction and risk of breast cancer. Br. J. Cancer 114, 125–133. https://doi.org/10.1038/bjc.2015.439
Samarghandian, S., Shoshtari, M.E., Sargolzaei, J., Hossinimoghadam, H., Farahzad, J.A., 2014. Anti-tumor activity of safranal against neuroblastoma cells. Pharmacogn. Mag. 10(Suppl 2), S419–S424. https://doi.org/10.4103/0973-1296.133296
Saxton, R.A., Sabatini, D.M., 2017. mTOR signaling in cancer. Cell 168, 960. https://doi.org/10.1016/j.cell.2017.02.004
Sirelkhatim, A., Mahmud, S., Seeni, A., Kaus, N.H.M., Ann, L.C., Bakhori, S.K.M., Hasan, H., Mohamad, D., 2015. Review on Zinc Oxide Nanoparticles: Antibacterial Activity and Toxicity Mechanism. Nano-Micro Lett. 7(3), 219–242. https://doi.org/10.1007/s40820-015-0040-x
Tajmehri, H., Mousavi, F.S., Heydarnezhad, M., Golrokh, F.J., Nezami, P.V., Khanpour, P., Ghafardoust Noroudi, S., Salehzadeh, A., 2024. Evaluation of the cytotoxic effect of cobalt oxide nanoparticles functionalized by glucose and conjugated with lapatinib (Co3O4@Glu-Lapatinib) on a lung cancer cell line and evaluation of the expression of CASP8, mTOR1, and MAPK1 genes. BioNanoScience 14, 999–1010. https://doi.org/10.1007/s12668-024-01348-6
Wang, B., Chen, N., Wei, Y., Li, J., Sun, L., Wu, J., Huang, Q., Liu, C., Fan, C., Song, H., 2012. Functional properties of nanomaterials in biological systems. Sci. Rep. 2, 563. https://doi.org/10.1038/srep00563
Wang, J., Chen, Y., Lu, D., Chen, Y., Jia, Y., Ying, X., Xiong, H., Zhao, W., Zhou, J., Wang, L., 2017. Matrix metalloproteinase-1 expression in breast carcinoma: a marker for unfavorable prognosis. Oncotarget 8, 91379–91390. https://doi.org/10.18632/oncotarget.20557
Wang, J., Deng, X., Zhang, F., Chen, D., Ding, W., 2014. ZnO nanoparticle-induced oxidative stress triggers apoptosis by activating JNK signaling pathway in cultured primary astrocytes. Nanoscale Res. Lett. 9, 117. https://doi.org/10.1186/1556-276X-9-117
Wang, S.W., Lee, C.H., Lin, M.S., Chi, C.W., Chen, Y.J., Wang, G.S., Liao, K.W., Chiu, L.P., Wu, S.H., Huang, D.M., Chen, L., Shen, Y.S., 2020. ZnO nanoparticles induced caspase-dependent apoptosis in gingival squamous cell carcinoma through mitochondrial dysfunction and p70S6K signaling pathway. Int. J. Mol. Sci. 21(5), 1612. https://doi.org/10.3390/ijms21051612
Wan, R., Mo, Y., Chien, S., Li, Y., Tollerud, D.J., Zhang, Q., 2011. The role of hypoxia inducible factor-1α in the increased MMP-2 and MMP-9 production by human monocytes exposed to nickel nanoparticles. Nanotoxicology 5(4), 568-582. https://doi.org/10.3109/17435390.2010.537791
Wu, Y., Zhang, Q., Ruan, Z., Yin, Y., 2016. Intrinsic effects of gold nanoparticles on proliferation and invasion activity in SGC-7901 cells. Oncol. Rep. 35(3), 1457-1462. https://doi.org/10.3892/or.2015.4474
Zhang, Y., Chen, W., Wang, S., Liu, Y., Pope, C., 2008. Phototoxicity of zinc oxide nanoparticle conjugates in human ovarian cancer NIH: OVCAR-3 cells. J. Biomed. Nanotechnol. 4, 432–438. https://doi.org/10.1166/jbn.2008.006
Zhang, Q., Ma, Y., Yang, S., Xu, B., Fei, X., 2015. Small-sized gold nanoparticles inhibit the proliferation and invasion of SW579 cells. Mol. Med. Rep. 12(6), 8313-8319. https://doi.org/10.3892/mmr.2015.4433
Zhang, X., Yin, H., Li, Z., Zhang, T., Yang, Z., 2016. Molecular mechanisms of nanoparticle-induced cytotoxicity. Cell Biol. Toxicol. 32, 513. https://doi.org/10.1007/s10565-016-9352-y | ||
|
آمار تعداد مشاهده مقاله: 303 تعداد دریافت فایل اصل مقاله: 93 |
||