PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 31992334-9 2020 Furthermore, CD44-positive HCC PDOs were obviously resistant to sorafenib, and sorafenib increased CD44 levels. Sorafenib 64-73 CD44 molecule (Indian blood group) Homo sapiens 13-17 33199679-8 2020 More importantly, the treatment of HCC cells expressing CD44 (the main PRG4 receptor) with rhPRG4 dramatically enhances the growth-limiting capacity of sorafenib and regorafenib, whereas not significantly affecting cell proliferation per se. Sorafenib 152-161 CD44 molecule (Indian blood group) Homo sapiens 56-60 31992334-9 2020 Furthermore, CD44-positive HCC PDOs were obviously resistant to sorafenib, and sorafenib increased CD44 levels. Sorafenib 79-88 CD44 molecule (Indian blood group) Homo sapiens 99-103 31992334-11 2020 In addition, there was a highly synergistic effect in vitro and in vivo on the suppression of cell viability and malignant properties when sorafenib and GANT61 were added to CD44-positive HCC PDOs and cell lines, respectively. Sorafenib 139-148 CD44 molecule (Indian blood group) Homo sapiens 174-178 31992334-12 2020 Furthermore, the upregulation of CD44 and Hedgehog signaling induced by sorafenib was reversed by GANT61. Sorafenib 72-81 CD44 molecule (Indian blood group) Homo sapiens 33-37 31992334-13 2020 CONCLUSIONS: GANT61 significantly suppressed Hedgehog signaling to reverse sorafenib resistance in CD44-positive HCC. Sorafenib 75-84 CD44 molecule (Indian blood group) Homo sapiens 99-103 31992334-14 2020 The combination of sorafenib and Hedgehog signaling inhibitors might be effective in HCC patients with high CD44 levels as a personalized-medicine approach. Sorafenib 19-28 CD44 molecule (Indian blood group) Homo sapiens 108-112 31992334-9 2020 Furthermore, CD44-positive HCC PDOs were obviously resistant to sorafenib, and sorafenib increased CD44 levels. Sorafenib 79-88 CD44 molecule (Indian blood group) Homo sapiens 13-17 28627617-0 2017 Sorafenib controls the epithelial-mesenchymal transition of ovarian cancer cells via EGF and the CD44-HA signaling pathway in a cell type-dependent manner. Sorafenib 0-9 CD44 molecule (Indian blood group) Homo sapiens 97-101 29899840-5 2018 CD44 was significantly increased in Huh7 cells made resistant to sorafenib. Sorafenib 65-74 CD44 molecule (Indian blood group) Homo sapiens 0-4 29899840-10 2018 Moreover, a combination of INK128 and sorafenib showed improved anti-proliferative effects in CD44high HCC cells. Sorafenib 38-47 CD44 molecule (Indian blood group) Homo sapiens 94-98 29899840-12 2018 Since the clinical response to sorafenib is highly variable, our findings suggest that ATP-competitive mTOR inhibitors may be effective in treating advanced, CD44-expressing HCC patients who are insensitive to sorafenib. Sorafenib 31-40 CD44 molecule (Indian blood group) Homo sapiens 158-162 25053293-8 2015 Targeted CD44 knock-down in the mesenchymal-like cells indicated that CD44 plays an active role in protecting HCC cells from sorafenib-induced apoptosis. Sorafenib 125-134 CD44 molecule (Indian blood group) Homo sapiens 9-13 25053293-8 2015 Targeted CD44 knock-down in the mesenchymal-like cells indicated that CD44 plays an active role in protecting HCC cells from sorafenib-induced apoptosis. Sorafenib 125-134 CD44 molecule (Indian blood group) Homo sapiens 70-74 25053293-10 2015 In conclusion, a mesenchymal profile and expression of CD44, linked to activation of the TGF-beta pathway, may predict lack of response to sorafenib in HCC patients. Sorafenib 139-148 CD44 molecule (Indian blood group) Homo sapiens 55-59 23228386-13 2013 Hymecromone plus sorafenib up-regulated pro-apoptotic indicators and down-regulated Mcl-1, CD44, RHAMM, phospho-epidermal growth factor receptor and phospho-cMet. Sorafenib 17-26 CD44 molecule (Indian blood group) Homo sapiens 91-95 23314174-6 2013 Notably, the combination of sorafenib and radiation eliminated CD44+CD24-/low cells preferentially, which highly expressed hypoxia-inducible factor (HIF)-1alpha and effectively inhibited primary and secondary mammosphere formation in MDA-MB-231 cells. Sorafenib 28-37 CD44 molecule (Indian blood group) Homo sapiens 63-67 27461522-6 2016 Sorafenib diminished the self-renewal capacity and downregulated the expression of stem cell biomarkers (CD133, CD44 and ALDH1) in a dose-dependent manner, while BrMC cooperated with sorafenib to strengthen this inhibition. Sorafenib 0-9 CD44 molecule (Indian blood group) Homo sapiens 112-116