2022
DOI: 10.1016/j.tiv.2022.105328
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Nickel nanoparticles affect the migration and invasion of HTR-8/SVneo cells by downregulating MMP2 through the PI3K/AKT pathway

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Cited by 7 publications
(5 citation statements)
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“…54 The Akt signaling pathway plays a pivotal role in regulating various cellular processes, including cell invasion, apoptosis and migration and has attracted increasing attention for anti-cancer therapeutics. 55,56 Presently, we found that CCL3-CCR5 interaction could enhance the migratory and invasive capabilities of COAD cells by activating the Akt signaling pathway, which was consistent with previous studies. Furthermore, we examined whether CCL3 derived from dence has illustrated that MMPs such as MMP-2/9 were important markers for tumor metastasis.…”
Section: Discussionsupporting
confidence: 92%
See 1 more Smart Citation
“…54 The Akt signaling pathway plays a pivotal role in regulating various cellular processes, including cell invasion, apoptosis and migration and has attracted increasing attention for anti-cancer therapeutics. 55,56 Presently, we found that CCL3-CCR5 interaction could enhance the migratory and invasive capabilities of COAD cells by activating the Akt signaling pathway, which was consistent with previous studies. Furthermore, we examined whether CCL3 derived from dence has illustrated that MMPs such as MMP-2/9 were important markers for tumor metastasis.…”
Section: Discussionsupporting
confidence: 92%
“…Akt is a serine–threonine protein kinase which can be phosphorylated at Thr308 and Ser473 by PDK1 and mTORC2, respectively 54 . The Akt signaling pathway plays a pivotal role in regulating various cellular processes, including cell invasion, apoptosis and migration and has attracted increasing attention for anti‐cancer therapeutics 55,56 . Presently, we found that CCL3‐CCR5 interaction could enhance the migratory and invasive capabilities of COAD cells by activating the Akt signaling pathway, which was consistent with previous studies.…”
Section: Discussionsupporting
confidence: 89%
“…123 Stimulating human epidermal keratinocytes with 20 μg/mL (noncytotoxic dose) 124 or stimulating human monocytes with 30 μg/mL (noncytotoxic dose) CuO 125 can upregulate the expression of MMP2 and MMP9 and stimulate human villous trophoblast cell lines. Finally, stimulation with 100 μg/mL (cytotoxic dose) 126 can inhibit the expression of MMP2. However, the regulated pathways differed among these groups.…”
Section: Glycosaminoglycanmentioning
confidence: 99%
“…30 Cytotoxic, genotoxic, and apoptotic effects of NiO NPs were also observed in human intestinal epithelial cells (Caco-2). 125 Moreover, Nicontaining NPs can also cause cytotoxicity in other types of cells including monocytes, [126][127][128] neutrophils, 129 lymphocytes, 130 RBCs, 131 endothelial progenitor cells, 132,133 endothelial cells, 134,135 spermatogonial cells (GC-1 spg), 136 trophoblasts (HTR-8/SVneo), 137,138 Sertoli-germ cells, 139 mesenchymal stem cells, 140 adipose stem cells, 141 pleural mesothelial 2 cells (NRM2), 142 kidney cells (NRK-52E), 143 skeletal myoblasts (L-6), 144 etc.…”
Section: Extra-pulmonary Effects Of Nicontaining Npsmentioning
confidence: 99%