PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 11029783-8 2000 Docetaxel increased IL-6 levels in both serum and KPL-4 tumors, but combined treatment with docetaxel and 5"-DFUR resulted not only in a potent antitumor effect but also in a drastic decrease of serum IL-6 levels. Docetaxel 0-9 interleukin 6 Homo sapiens 20-24 19014338-9 2009 Elevated IL-6 levels and reductions in IL-6 levels early in treatment may reflect ultimate clinical response to docetaxel-based regimens. Docetaxel 112-121 interleukin 6 Homo sapiens 9-13 19014338-9 2009 Elevated IL-6 levels and reductions in IL-6 levels early in treatment may reflect ultimate clinical response to docetaxel-based regimens. Docetaxel 112-121 interleukin 6 Homo sapiens 39-43 12085250-13 2002 The present study indicates that patients responded to treatment of advanced breast cancer with single-agent paclitaxel or docetaxel leads to an increase in serum IFN-gamma, IL-2, IL-6, GM-CSF cytokine levels and enhancement of PBMC NK and LAK cell activity, while they both lead to a decrease of acute phase serum cytokine levels of IL-1 and TNF-alpha. Docetaxel 123-132 interleukin 6 Homo sapiens 180-184 11710628-0 2001 Combined effects of docetaxel and fluoropyrimidines on tumor growth and expression of interleukin-6 and thymidine phosphorylase in breast cancer xenografts. Docetaxel 20-29 interleukin 6 Homo sapiens 86-99 11710628-9 2001 In addition, combined treatment with docetaxel and oral fluoropyrimidines may decrease serum IL-6 levels and may ameliorate IL-6-induced cancer cachexia. Docetaxel 37-46 interleukin 6 Homo sapiens 93-97 11710628-9 2001 In addition, combined treatment with docetaxel and oral fluoropyrimidines may decrease serum IL-6 levels and may ameliorate IL-6-induced cancer cachexia. Docetaxel 37-46 interleukin 6 Homo sapiens 124-128 21214673-3 2011 Changes in the growth and sensitivity to docetaxel in PC3/sh-IL6 were compared with those in PC3 transfected with control vector alone (PC3/Co). Docetaxel 41-50 interleukin 6 Homo sapiens 61-64 21214673-6 2011 Despite the higher sensitivity of PC3/sh-IL6 to docetaxel than that of PC3/Co, the secretion of IL-6 by both cell lines was increased after treatment with docetaxel due to the formation of positive autocrine loops between these cell lines and NFkappaB signaling pathways. Docetaxel 48-57 interleukin 6 Homo sapiens 41-44 21214673-6 2011 Despite the higher sensitivity of PC3/sh-IL6 to docetaxel than that of PC3/Co, the secretion of IL-6 by both cell lines was increased after treatment with docetaxel due to the formation of positive autocrine loops between these cell lines and NFkappaB signaling pathways. Docetaxel 155-164 interleukin 6 Homo sapiens 41-44 21214673-6 2011 Despite the higher sensitivity of PC3/sh-IL6 to docetaxel than that of PC3/Co, the secretion of IL-6 by both cell lines was increased after treatment with docetaxel due to the formation of positive autocrine loops between these cell lines and NFkappaB signaling pathways. Docetaxel 155-164 interleukin 6 Homo sapiens 96-100 21214673-7 2011 Furthermore, combined treatment with the proteasome inhibitor bortezomib, which completely inhibited the docetaxel-induced IL-6 secretion via the inactivation of NFkappaB signaling, resulted in the marked sensitization of these cell lines to docetaxel both in vitro and in vivo. Docetaxel 105-114 interleukin 6 Homo sapiens 123-127 21214673-8 2011 These findings suggest that suppressed IL-6 secretion using shRNA, either alone or in combination with docetaxel and bortezomib, could be a useful therapeutic strategy against androgen-independent prostate cancer. Docetaxel 103-112 interleukin 6 Homo sapiens 39-43 12085250-12 2002 More specifically, docetaxel demonstrated a more pronounced effect on enhancing MLR, NK, LAK activity and IFN-gamma, IL-2, IL-6, and GM-CSF levels, as well as caused more potent reduction in IL-1 and TNF-alpha levels when compared to paclitaxel. Docetaxel 19-28 interleukin 6 Homo sapiens 123-127 11029783-8 2000 Docetaxel increased IL-6 levels in both serum and KPL-4 tumors, but combined treatment with docetaxel and 5"-DFUR resulted not only in a potent antitumor effect but also in a drastic decrease of serum IL-6 levels. Docetaxel 92-101 interleukin 6 Homo sapiens 201-205 28259909-7 2017 CACNAD2A3, GDF5 and IL6 were upregulated and NANOG was downregulated in the MCF7 breast cancer cells expressing increased levels of PAR4 after treatment with docetaxel, likely indicating inactivation of the WNT/beta-catenin pathway. Docetaxel 158-167 interleukin 6 Homo sapiens 20-23 34862831-9 2022 EEP + DTX exerted no cytotoxic effects on monocytes and stimulated HLA-DR expression, TNF-alpha, and IL-6 production, exerted an immunorestorative action in the fungicidal activity, and reduced the oxidative stress. Docetaxel 6-9 interleukin 6 Homo sapiens 101-105 29565447-21 2018 Univariate and multivariate analyses revealed that age, CA125, interstitial IL-6 expression and cytoreduction satisfaction were closely related to the sensitivity of the TP (docetaxel plus cisplatin or carbopatin) regimen in ovarian cancer (P<0.05). Docetaxel 174-183 interleukin 6 Homo sapiens 76-80 34293716-10 2021 Consistent with this model, the overexpression of IL-6 reversed the OGFRP1 knockdown-mediated reductions in docetaxel and paclitaxel IC50 values for these PC cells. Docetaxel 108-117 interleukin 6 Homo sapiens 50-54 31412584-3 2019 Docetaxel or vinorelbine inhibits proliferation and stimulates the differentiation of breast preadipocytes, by increasing C/EBPalpha and PPARgamma expression and by downregulating tumor necrosis factor alpha (TNFalpha), interleukin 6 (IL-6), and IL-11 expression. Docetaxel 0-9 interleukin 6 Homo sapiens 220-233 31412584-3 2019 Docetaxel or vinorelbine inhibits proliferation and stimulates the differentiation of breast preadipocytes, by increasing C/EBPalpha and PPARgamma expression and by downregulating tumor necrosis factor alpha (TNFalpha), interleukin 6 (IL-6), and IL-11 expression. Docetaxel 0-9 interleukin 6 Homo sapiens 235-239 26528857-8 2015 In line with the above findings, treatment with either IL-3 or IL-6 or IL-11 decreased the chemosensitivity to docetaxel while treatment with either IL-10 or IL-24 increased the sensitivity of docetaxel chemotherapy. Docetaxel 111-120 interleukin 6 Homo sapiens 63-67 26194374-6 2016 In the TSU-68 plus docetaxel group, PFS showed significant association with fold changes in CRP (p=0.001), IL-6 (p < .001), PDGF-BB (p=0.02), and VEGF (p=0.047) following the first treatment cycle. Docetaxel 19-28 interleukin 6 Homo sapiens 107-111 24939178-7 2014 Together, our data provide a novel explanation that high level of IL6 stimulated SOD2 expression that, at least partially, contributed to the low level of ROS that would likely result in a sustained increase in the expression of IGF-1R through abolishment of beta-arrestin1 in docetaxel resistant cells. Docetaxel 277-286 interleukin 6 Homo sapiens 66-69 24939178-0 2014 Regulation of SOD2 and beta-arrestin1 by interleukin-6 contributes to the increase of IGF-1R expression in docetaxel resistant prostate cancer cells. Docetaxel 107-116 interleukin 6 Homo sapiens 41-54 23038213-0 2013 Nuclear factor-kappa B and interleukin-6 related docetaxel resistance in castration-resistant prostate cancer. Docetaxel 49-58 interleukin 6 Homo sapiens 27-40