PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 34765016-0 2021 Shikonin regulates autophagy via the AMPK/mTOR pathway and reduces apoptosis of human umbilical cord mesenchymal stem cells to improve survival in tissues surrounding brain contusion. shikonin 0-8 mechanistic target of rapamycin kinase Homo sapiens 42-46 34765016-1 2021 Shikonin has been reported to regulate autophagy via the AMP-activated protein kinase (AMPK)/mTOR signalling pathway and decrease apoptosis in transplanted human umbilical cord mesenchymal stem cells (HUMSCs). shikonin 0-8 mechanistic target of rapamycin kinase Homo sapiens 93-97 34765016-3 2021 Differences in autophagy and AMPK/mTOR pathway-related protein expression following treatment with shikonin were quantitatively analyzed by western blotting. shikonin 99-107 mechanistic target of rapamycin kinase Homo sapiens 34-38 34812264-0 2021 Shikonin Promotes Apoptosis and Attenuates Migration and Invasion of Human Esophageal Cancer Cells by Inhibiting Tumor Necrosis Factor Receptor-Associated Protein 1 Expression and AKT/mTOR Signaling Pathway. shikonin 0-8 mechanistic target of rapamycin kinase Homo sapiens 184-188 34812264-11 2021 More interestingly, we demonstrated that shRNA-TRAP1 played a synergistic role in shikonin-mediated regulation of protein kinase B (AKT)/mammalian target of rapamycin (mTOR) signaling. shikonin 82-90 mechanistic target of rapamycin kinase Homo sapiens 137-166 34812264-11 2021 More interestingly, we demonstrated that shRNA-TRAP1 played a synergistic role in shikonin-mediated regulation of protein kinase B (AKT)/mammalian target of rapamycin (mTOR) signaling. shikonin 82-90 mechanistic target of rapamycin kinase Homo sapiens 168-172 34812264-12 2021 Collectively, shikonin promoted apoptosis and attenuated migration and invasion of EC cells by inhibiting TRAP1 expression and AKT/mTOR signaling, indicating that shikonin may be a new drug for treating EC. shikonin 14-22 mechanistic target of rapamycin kinase Homo sapiens 131-135 34812264-12 2021 Collectively, shikonin promoted apoptosis and attenuated migration and invasion of EC cells by inhibiting TRAP1 expression and AKT/mTOR signaling, indicating that shikonin may be a new drug for treating EC. shikonin 163-171 mechanistic target of rapamycin kinase Homo sapiens 131-135 33334200-0 2021 Shikonin induces odontoblastic differentiation of dental pulp stem cells via AKT-mTOR signaling in the presence of CD44. shikonin 0-8 mechanistic target of rapamycin kinase Homo sapiens 81-85 33334200-6 2021 Shikonin-induced expression of DSPP was inhibited by PI3K, AKT, and mTOR inhibitors. shikonin 0-8 mechanistic target of rapamycin kinase Homo sapiens 68-72 33334200-8 2021 Conclusions: Shikonin can stimulate dental pulp stem cells to undergo odontoblastic differentiation through a mechanism involving the AKT-mTOR signaling pathway and CD44. shikonin 13-21 mechanistic target of rapamycin kinase Homo sapiens 138-142 33334200-9 2021 Although expression of CD44 is important for inducing odontoblastic differentiation of dental pulp stem cells, the relationship between the AKT-mTOR signaling pathway and CD44 expression, in the context of shikonin stimulation, has not yet been elucidated. shikonin 206-214 mechanistic target of rapamycin kinase Homo sapiens 144-148 29449346-0 2018 Shikonin suppresses proliferation and induces apoptosis in endometrioid endometrial cancer cells via modulating miR-106b/PTEN/AKT/mTOR signaling pathway. shikonin 0-8 mechanistic target of rapamycin kinase Homo sapiens 130-134 35267423-0 2022 Shikonin Inhibits Cell Growth of Sunitinib-Resistant Renal Cell Carcinoma by Activating the Necrosome Complex and Inhibiting the AKT/mTOR Signaling Pathway. shikonin 0-8 mechanistic target of rapamycin kinase Homo sapiens 133-137 24905636-0 2014 Shikonin inhibits prostate cancer cells metastasis by reducing matrix metalloproteinase-2/-9 expression via AKT/mTOR and ROS/ERK1/2 pathways. shikonin 0-8 mechanistic target of rapamycin kinase Homo sapiens 112-116 24905636-7 2014 In addition, shikonin significantly decreased the phosphorylation of AKT and mTOR in a dose-dependent manner while it induced extracellular signal-regulated kinase (ERK), p38 mitogen activated protein kinase (MAPK) and c-Jun N terminal kinase (JNK) phosphorylation. shikonin 13-21 mechanistic target of rapamycin kinase Homo sapiens 77-81 24905636-10 2014 Together, shikonin inhibits aggressive prostate cancer cell migration and invasion by reducing MMP-2/-9 expression via AKT/mTOR and ROS/ERK1/2 pathways and presents a potential novel alternative agent for the treatment of human prostate cancer. shikonin 10-18 mechanistic target of rapamycin kinase Homo sapiens 123-127