PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 19276356-1 2009 p21 loss has been implicated in conferring oncogenic activity to known tumor suppressor gene KLF4 and cancer drug tamoxifen. Tamoxifen 114-123 H3 histone pseudogene 16 Homo sapiens 0-3 23361053-2 2013 The p21-regulated serine/threonine kinase PAK1, implicated in tamoxifen resistance, phosphorylates EBP1 in vitro and in vivo at T261. Tamoxifen 62-71 H3 histone pseudogene 16 Homo sapiens 4-7 22589186-6 2012 Furthermore, we show that Tam- and siE6AP-mediated inhibition of E6AP leads to enhanced G0-G1 growth arrest and apoptosis, which is also evident from significant upregulation of cytochrome-c, Bax, p21, and PARP cleavage. Tamoxifen 26-29 H3 histone pseudogene 16 Homo sapiens 197-200 21922150-9 2012 Treatment of PA-1 cells with 10 microM tamoxifen resulted in an increase in the levels of p21, p27, p16 and phospho-pRb, indicating typical G1 arrest. Tamoxifen 39-48 H3 histone pseudogene 16 Homo sapiens 102-105 20086099-8 2010 It has been known that p21 is required for a proper tamoxifen response in breast cancer. Tamoxifen 52-61 H3 histone pseudogene 16 Homo sapiens 23-26 20086099-9 2010 We show that the overexpression of 14-3-3tau inhibits tamoxifen-induced p21 induction and growth arrest in MCF7 cells. Tamoxifen 54-63 H3 histone pseudogene 16 Homo sapiens 72-75 10661763-4 1999 In this model, TAM resistance resulted in an increase in the detectable basal levels of cyclin E, GADD 153, p16, BAX, Bcl-XL, and wild-type and mutant p53, an increase in TAM induction of p16, and a decrease in the detectable basal levels of cyclin D1, p21 and p27. Tamoxifen 15-18 H3 histone pseudogene 16 Homo sapiens 253-256 14633737-9 2003 Treatment with Let, Tam, or E2W resulted in a dose- and time-dependent increase in active caspase-7 and up-regulation of p53 and p21 protein. Tamoxifen 20-23 H3 histone pseudogene 16 Homo sapiens 129-132 10661763-6 1999 In the TAM-resistant variant, p21 levels were essentially undetectable, while p27 was present and maintained its response to TAM Induction, albeit at a much lower level. Tamoxifen 7-10 H3 histone pseudogene 16 Homo sapiens 30-33 32722075-8 2020 In addition, LY and TAM combination induced the apoptotic genes Caspase-3, Caspase-7, and p53, as well as p21 as cell cycle promotor, and significantly downregulated the anti-apoptotic genes Bcl-2 and survivin. Tamoxifen 20-23 H3 histone pseudogene 16 Homo sapiens 106-109 9199341-2 1997 Addition of estradiol relieves the cell cycle block created by tamoxifen treatment, leading to marked activation of cyclin E-cdk2 complexes and phosphorylation of the retinoblastoma protein within 6 h. Cyclin D1 levels increase significantly while the levels of cyclin E, cdk2, and the p21 and p27 cdk inhibitors are relatively constant. Tamoxifen 63-72 H3 histone pseudogene 16 Homo sapiens 286-289 27432642-6 2016 The present study also demonstrated that combinational treatment is more effective in inducing G1 phase arrest and activating apoptosis compared tamoxifen alone, which may be due to upregulation of P21 expression and downregulation of the B-cell CLL/lymphoma 2(Bcl-2)/Bcl-2 associated X protein ratio. Tamoxifen 145-154 H3 histone pseudogene 16 Homo sapiens 198-201 30628639-0 2019 Long non-coding RNA UCA1 confers tamoxifen resistance in breast cancer endocrinotherapy through regulation of the EZH2/p21 axis and the PI3K/AKT signaling pathway. Tamoxifen 33-42 H3 histone pseudogene 16 Homo sapiens 119-122 25595558-7 2015 Consistent with this observation in SK-MEL28 cells, Sp1 was necessary for the tamoxifen-regulated Raf-1:ER to induce p21(CIP1) transcription in U251 cells, in which TP53 is mutated. Tamoxifen 78-87 H3 histone pseudogene 16 Homo sapiens 118-121