2021
DOI: 10.1080/03639045.2022.2072513
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Modulation of gene expression by thymoquinone conjugated zinc oxide nanoparticles arrested cell cycle, DNA damage and increased apoptosis in triple negative breast cancer cell line MDA-MB-231

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Cited by 6 publications
(5 citation statements)
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“…At the 24th hour, they showed that it caused higher toxicity in tumor cells . In another study, they coated TQ with a zinc oxide nanoparticle in the MDA-MB231 cell line, examined its effect on breast cancer cells, and showed by the flow cytometric method that it stopped DNA damage and cell cycle and increased apoptosis . Ibiyeye et al coated TQ with a CaCO 3 nanoparticle and investigated its antiproliferative effect on the same tumor cell line (MDA-MB231 cell line) and found that the IC 50 value of the TQ-CaCO 3 nanoparticle was higher than that of TQ.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…At the 24th hour, they showed that it caused higher toxicity in tumor cells . In another study, they coated TQ with a zinc oxide nanoparticle in the MDA-MB231 cell line, examined its effect on breast cancer cells, and showed by the flow cytometric method that it stopped DNA damage and cell cycle and increased apoptosis . Ibiyeye et al coated TQ with a CaCO 3 nanoparticle and investigated its antiproliferative effect on the same tumor cell line (MDA-MB231 cell line) and found that the IC 50 value of the TQ-CaCO 3 nanoparticle was higher than that of TQ.…”
Section: Discussionmentioning
confidence: 99%
“… 38 In another study, they coated TQ with a zinc oxide nanoparticle in the MDA-MB231 cell line, examined its effect on breast cancer cells, and showed by the flow cytometric method that it stopped DNA damage and cell cycle and increased apoptosis. 39 Ibiyeye et al coated TQ with a CaCO 3 nanoparticle and investigated its antiproliferative effect on the same tumor cell line (MDA-MB231 cell line) and found that the IC 50 value of the TQ-CaCO 3 nanoparticle was higher than that of TQ. However, the combination therapy showed improved apoptosis, reduced intracellular migration, and reduced invasion when compared with single drug-loaded nanoparticles and free drugs.…”
Section: Discussionmentioning
confidence: 99%
“…Ruenraroengsak et al used ZnONPs combined with anti-FZD-7 antibodies to target and kill highly expressing FZD-7 breast cancer cells, highlighting the potential clinical application value of this nanoplatform [ 107 ]. Recently, Sjs et al combined Thymoquinone (TQ) with ZnONPs to yield TQ-ZnO nanoparticles that inhibited breast cancer cell proliferation, increased DNA damage, and led to apoptosis in the TNBC cell line MDA-MB-231 [ 108 ]. In addition to chemotherapy and targeted immunotherapy, ZnO was used for the synthesis of chitosan-ZnO biological nanocomposites (CS-ZnO BNCs) as radiosensitizers to enhance the effect of radiation therapy in breast cancer models, reflecting advantages in radiation therapy [ 109 ].…”
Section: Zinc Oxide Nanoparticles and Breast Cancermentioning
confidence: 99%
“…Moreover, due to the selective interaction with the folate receptors on MCF‐7 cells, this nanohybrid system reduced the IC 50 by 20–30 folds compared to free eugenol (Uma Maheswari et al, 2021). TQ incorporated zinc oxide NPs exhibited enhanced anticancer activity against MDA‐MB‐231 cells by inducing G2/M phase cell cycle arrest, DNA damage and apoptosis (Sjs et al, 2021). Zhang et al demonstrated that loading of curcumol into a pH responsive, metal–organic frameworks using porphyrin and Cu 2+ (CUR‐CuTPyP/F68) facilitated efficient accumulation and internalization in tumor cells.…”
Section: Nanoencapsulation Of Eos and Their Constituentsmentioning
confidence: 99%