PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 29349515-11 2018 Interestingly, in hydroxychloroquine or topical corticosteroid-treated patients, MMP-2/-9 activity levels were found to be higher compared to untreated patients. Hydroxychloroquine 18-36 matrix metallopeptidase 2 Homo sapiens 81-89 34278709-0 2021 Attenuation of chloroquine and hydroxychloroquine on the invasive potential of bladder cancer through targeting matrix metalloproteinase 2 expression. Hydroxychloroquine 31-49 matrix metallopeptidase 2 Homo sapiens 112-138 34278709-4 2021 In this study, CQ and HCQ treatments inhibited the migration and invasion of two BC cell types (5637 and T24) through expression modulation of matrix metalloproteinase-2 (MMP-2), which belongs to the matrix MMP family and is a key mediator of cancer progression. Hydroxychloroquine 22-25 matrix metallopeptidase 2 Homo sapiens 143-169 34278709-4 2021 In this study, CQ and HCQ treatments inhibited the migration and invasion of two BC cell types (5637 and T24) through expression modulation of matrix metalloproteinase-2 (MMP-2), which belongs to the matrix MMP family and is a key mediator of cancer progression. Hydroxychloroquine 22-25 matrix metallopeptidase 2 Homo sapiens 171-176 34278709-4 2021 In this study, CQ and HCQ treatments inhibited the migration and invasion of two BC cell types (5637 and T24) through expression modulation of matrix metalloproteinase-2 (MMP-2), which belongs to the matrix MMP family and is a key mediator of cancer progression. Hydroxychloroquine 22-25 matrix metallopeptidase 2 Homo sapiens 207-210 34278709-6 2021 In conclusion, our research demonstrated that CQ and HCQ regulated cell motility in BC through MMP-2 downregulation by targeting autophagy functions, providing a novel therapeutic strategy for BC treatment. Hydroxychloroquine 53-56 matrix metallopeptidase 2 Homo sapiens 95-100 34182874-6 2021 METHODS: In this research, to explore the effect of HCQ for angiogenesis, we investigated: (1) Human umbilical vein endothelial cells (HUVECs) viability by CCK-8; (2) HUVECs migration by wound healing; (3) HUVEC angiogenesis by Matrigel assay in vitro; (4) mRNA expression of MMP-2 and VEGF by real-time quantitative Polymerase Chain Reaction (RT-PCR); (5) protein expression of VEGF, MMP-2 by western blot. Hydroxychloroquine 52-55 matrix metallopeptidase 2 Homo sapiens 276-281 34182874-6 2021 METHODS: In this research, to explore the effect of HCQ for angiogenesis, we investigated: (1) Human umbilical vein endothelial cells (HUVECs) viability by CCK-8; (2) HUVECs migration by wound healing; (3) HUVEC angiogenesis by Matrigel assay in vitro; (4) mRNA expression of MMP-2 and VEGF by real-time quantitative Polymerase Chain Reaction (RT-PCR); (5) protein expression of VEGF, MMP-2 by western blot. Hydroxychloroquine 52-55 matrix metallopeptidase 2 Homo sapiens 385-390 34182874-7 2021 RESULTS: We found that HCQ treatment significantly restored the expression of aPL-inhibited VEGF and MMP-2. Hydroxychloroquine 23-26 matrix metallopeptidase 2 Homo sapiens 101-106