PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 29960296-4 2017 RESULTS: In BGC-823 and MGC-803 gastric cancer cells treated with 80, 120, and 160 mumol/L baicalinfor 48 h, a 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide assay showed thatbaicalin significantly inhibited cell proliferation in a dose-dependent manner, while flow cytometricanalysis demonstrated that baicalin could induce apoptosis, also in a dose-dependent manner.Moreover, baicalin up-regulated the expression of caspase-3, caspase-9, and B cell lymphoma(Bcl-2)-associated X protein and down-regulated the expression of Bcl-2 at both the mRNA andprotein level. baicalin 91-99 caspase 3 Homo sapiens 437-446 26688183-7 2016 Western blot and real-time PCR analysis revealed that significant decrease in caspase-3 expression in the baicalin group compared with the OGD/RO group (P<0.01). baicalin 106-114 caspase 3 Homo sapiens 78-87 26309548-6 2015 Moreover, baicalin induced apoptotic cell death in Hep G2 and SMMC-7721 cells, which was accompanied by upregulation of Bax, downregulation of Bcl-2, and cleavages of Caspase-9, Caspase-3, and PARP. baicalin 10-18 caspase 3 Homo sapiens 178-187 22607709-7 2012 CA46 cells underwent apoptosis in response to baicalin treatment as evidenced by an increase in the percentage of cells stainable with Annexin V, by increased DNA fragmentation, and by activation of the intrinsic (mitochondrial) pathway for cell death as characterized by increased expression of the cleaved forms of caspase-9, caspase-3, and poly (ADP-ribose) polymerase. baicalin 46-54 caspase 3 Homo sapiens 328-337 25561931-7 2015 These results indicated that baicalin-induced apoptosis involved activation Caspase-3 in HeLa cells through the intracellular mitochondrial pathway and the surface death receptor pathway. baicalin 29-37 caspase 3 Homo sapiens 76-85 25694047-7 2015 Furthermore, baicalin-copper treatment significantly increased the Bax/Bcl-2 ratio and p38 levels, as well as decreased the expression of caspase-3, p-PI3K, p-Akt and p-mTOR (P < 0.01). baicalin 13-21 caspase 3 Homo sapiens 138-147 31223113-6 2019 Baicalin (200 mug/mL) significantly promoted the apoptosis of keratinocytes, arrested the S phase, inhibited the mRNA expression of ki67, increased the Fas and caspase-3 levels, down-regulated the protein expression of Jagged 1, and up-regulated the Notch 1 and Hes protein levels. baicalin 0-8 caspase 3 Homo sapiens 160-169 17352223-4 2007 The results showed that baicalin induced cytotoxicity in a dose- and time-dependent manner through the activation of caspase-3, as shown by treatment of HL-60 cells with an inhibitor of caspase-3 (z-VAD-fmk). baicalin 24-32 caspase 3 Homo sapiens 117-126 17352223-4 2007 The results showed that baicalin induced cytotoxicity in a dose- and time-dependent manner through the activation of caspase-3, as shown by treatment of HL-60 cells with an inhibitor of caspase-3 (z-VAD-fmk). baicalin 24-32 caspase 3 Homo sapiens 186-195 17352223-6 2007 Western blot demonstrated that baicalin promoted the levels of Gadd153, Bax, cytochrome c and caspase-3 and -12, but decreased the levels of Grp78 and Bcl-2 in HL-60 cells. baicalin 31-39 caspase 3 Homo sapiens 94-111 11053652-7 2000 The inhibition of proliferation of prostate cancer cells after a short period of exposure to baicalin was associated with induction by apoptosis, as evidenced by the typical nuclear fragmentation using Hoechst 33258 staining, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) labeling, DNA fragmentation, activation of caspase-3 and cleavage of poly-ADP-ribose polymerase (PARP). baicalin 93-101 caspase 3 Homo sapiens 347-356 35350754-9 2022 Result: A total of 86 overlapping targets of baicalin and CS were identified, among which MAPK14, IL2, FGF2, CASP3, PTGS2, PIK3CA, EGFR, and TNF were the core targets. baicalin 45-53 caspase 3 Homo sapiens 109-114 35573641-5 2022 Baicalin-induced apoptosis was confirmed by enhanced Bax, cleaved caspase-3, and cleaved PARP levels and decreased Bcl-2 levels. baicalin 0-8 caspase 3 Homo sapiens 66-75 32278854-10 2020 The anti-obesity effects of baicalin might be due to the up-regulation of solute carrier family 2 member 1 (SLC2A1) and down-regulation of tumor necrosis factor (TNF), nuclear factor kappa B subunit 1 (NFKB1), sterol regulatory element binding transcription factor 1 (SREBF1), peroxisome proliferator activated receptor gamma and caspase 3 (CASP3). baicalin 28-36 caspase 3 Homo sapiens 330-339 32278854-10 2020 The anti-obesity effects of baicalin might be due to the up-regulation of solute carrier family 2 member 1 (SLC2A1) and down-regulation of tumor necrosis factor (TNF), nuclear factor kappa B subunit 1 (NFKB1), sterol regulatory element binding transcription factor 1 (SREBF1), peroxisome proliferator activated receptor gamma and caspase 3 (CASP3). baicalin 28-36 caspase 3 Homo sapiens 341-346 31607304-14 2019 CONCLUSION: Baicalin derivative 02-036 can effectively inhibit the proliferation and induce apoptosis of CA46 cells, and its related mechanisms may be correlated with the down-regulation of apoptosis-related molecule expression levels, such as BCL-2, Pro-caspase-9, Pro-caspase-3, PARP and C-MYC. baicalin 12-20 caspase 3 Homo sapiens 266-279 22121772-8 2011 The further mechanism studies show that baicalin inhibit apoptosis via reducing Caspase-3 expression and up-regulating SIRT1. baicalin 40-48 caspase 3 Homo sapiens 80-89 16552836-8 2006 Baicalin (37.5 microg/ml) also elevated the amount of cytosolic cytochrome c (19.2 microg/ml), which finally triggered the activation of caspase-3 (50.1 pmol/min). baicalin 0-8 caspase 3 Homo sapiens 137-146 11841838-5 2002 Induction of apoptosis by baicalin was accompanied with the marginal generation of intracellular reactive oxygen species (ROS), the increase of the cytosolic fractions of cytochrome c, and the disruption of mitochondrial transmembrane potential (DeltaPsi(m)) prior to the activation of caspase-3. baicalin 26-34 caspase 3 Homo sapiens 286-295 31881375-8 2020 Baicalin inhibited cell proliferation, arrested the cell cycle at the G0/G1 phase, and induced cell death through caspase 3/7 activation. baicalin 0-8 caspase 3 Homo sapiens 114-125