Phase I and pharmacokinetic study of YM155, a small-molecule inhibitor of survivin.
about
Potential of apoptotic pathway-targeted cancer therapeutic research: Where do we stand?Targeting caspases in cancer therapeuticsProgress of molecular targeted therapies for prostate cancersSystems biology of cisplatin resistance: past, present and futureTargeting survivin in cancerTargeting the apoptosis pathway in hematologic malignanciesInterleukin enhancer-binding factor 3/NF110 is a target of YM155, a suppressant of survivinA novel small molecule FL118 that selectively inhibits survivin, Mcl-1, XIAP and cIAP2 in a p53-independent manner, shows superior antitumor activityAn intravenous (i.v.) route-compatible formulation of FL118, a survivin, Mcl-1, XIAP, and cIAP2 selective inhibitor, improves FL118 antitumor efficacy and therapeutic index (TI)A multicenter phase II study of sepantronium bromide (YM155) plus rituximab in patients with relapsed aggressive B-cell Non-Hodgkin lymphoma.RHAMM (CD168) is overexpressed at the protein level and may constitute an immunogenic antigen in advanced prostate cancer disease.Survivin, a molecular target for therapeutic interventions in squamous cell carcinoma.Survivin family proteins as novel molecular determinants of doxorubicin resistance in organotypic human breast tumors.Will targeting insulin growth factor help us or hurt us?: An oncologist's perspectiveSurvivin inhibition is critical for Bcl-2 inhibitor-induced apoptosis in hepatocellular carcinoma cells.Cell deathThe insulin-like growth factor-I receptor inhibitor figitumumab (CP-751,871) in combination with docetaxel in patients with advanced solid tumours: results of a phase Ib dose-escalation, open-label study.A cell-permeable dominant-negative survivin protein induces apoptosis and sensitizes prostate cancer cells to TNF-α therapy.Survivin knockdown increased anti-cancer effects of (-)-epigallocatechin-3-gallate in human malignant neuroblastoma SK-N-BE2 and SH-SY5Y cellsIdentification of BIRC6 as a novel intervention target for neuroblastoma therapy.Survivin is not induced by novel taxanes.Future perspectives in melanoma research: meeting report from the "Melanoma Bridge", Napoli, December 5th-8th 2013.Optimizing anti-gene oligonucleotide 'Zorro-LNA' for improved strand invasion into duplex DNA.pH-responsive artemisinin derivatives and lipid nanoparticle formulations inhibit growth of breast cancer cells in vitro and induce down-regulation of HER family members.YM155 down-regulates survivin and XIAP, modulates autophagy and induces autophagy-dependent DNA damage in breast cancer cells.Impacting tumor cell-fate by targeting the inhibitor of apoptosis protein survivinPhase II, multicenter, open-label, randomized study of YM155 plus docetaxel as first-line treatment in patients with HER2-negative metastatic breast cancer.Survivin knockdown and concurrent 4-HPR treatment controlled human glioblastoma in vitro and in vivo.Novel therapeutics for aggressive non-Hodgkin's lymphoma.Small molecule inhibitor YM155-mediated activation of death receptor 5 is crucial for chemotherapy-induced apoptosis in pancreatic carcinoma.Report of the EORTC-PAMM Meeting, Brussels, 16-18 March 2009: new strategies for a targeted and personalised therapy of cancer.A phase 2, multicenter, open-label study of sepantronium bromide (YM155) plus docetaxel in patients with stage III (unresectable) or stage IV melanomaTargeting Survivin Enhances Chemosensitivity in Retinoblastoma Cells and Orthotopic Tumors.Inhibition of Survivin with YM155 Induces Durable Tumor Response in Anaplastic Thyroid Cancer.Suppression of survivin promoter activity by YM155 involves disruption of Sp1-DNA interaction in the survivin core promoter.Anti-tumor activity of lipophilic imidazolium salts on select NSCLC cell linesPharmacokinetics of sepantronium bromide (YM155), a small-molecule suppressor of survivin, in Japanese patients with advanced solid tumors: dose proportionality and influence of renal impairment.High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy.Population pharmacokinetic modeling of sepantronium bromide (YM155), a small molecule survivin suppressant, in patients with non-small cell lung cancer, hormone refractory prostate cancer, or unresectable stage III or IV melanoma.Markedly additive antitumor activity with the combination of a selective survivin suppressant YM155 and alemtuzumab in adult T-cell leukemia.
P2860
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P2860
Phase I and pharmacokinetic study of YM155, a small-molecule inhibitor of survivin.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Phase I and pharmacokinetic study of YM155, a small-molecule inhibitor of survivin.
@en
type
label
Phase I and pharmacokinetic study of YM155, a small-molecule inhibitor of survivin.
@en
prefLabel
Phase I and pharmacokinetic study of YM155, a small-molecule inhibitor of survivin.
@en
P2093
P2860
P356
P1476
Phase I and pharmacokinetic study of YM155, a small-molecule inhibitor of survivin
@en
P2093
Alain Mita
Amita Patnaik
Anne Keating
Anthony W Tolcher
Chris Takimoto
Christopher R Garrett
Elizabeth Till
Kyri Papadopoulos
Lionel D Lewis
Pamela Bartels
P2860
P304
P356
10.1200/JCO.2008.17.2064
P407
P50
P577
2008-09-29T00:00:00Z