[HTML][HTML] Overactivation of Akt contributes to MEK inhibitor primary and acquired resistance in colorectal cancer cells

M Tsubaki, T Takeda, M Noguchi, M Jinushi, S Seki… - Cancers, 2019 - mdpi.com
RAS and BRAF-mutated colorectal cancers are associated with resistance to chemotherapy
and poor prognosis, highlighting the need for new therapeutic strategies. Although these …

Development and maintenance of a preclinical patient derived tumor xenograft model for the investigation of novel anti-cancer therapies

S Bagby, WA Messersmith, TM Pitts, A Capasso… - JoVE (Journal of …, 2016 - jove.com
Development and Maintenance of a Preclinical Patient Derived Tumor Xenograft Model for
the Investigation of Novel Anti-Cancer Therapies - JoVE JoVE JoVE Faculty Resource …

[HTML][HTML] Antitumor activity of the polo-like kinase inhibitor, TAK-960, against preclinical models of colorectal cancer

PJ Klauck, SM Bagby, A Capasso, EL Bradshaw-Pierce… - BMC cancer, 2018 - Springer
Abstract Background Polo-like kinase 1 (Plk1) is a serine/threonine kinase that is a key
regulator of multiple stages of mitotic progression. Plk1 is upregulated in many tumor types …

Photoactivation provides a mechanistic explanation for pan-assay interference behaviour of 2-aminopyrroles in lipoxygenase inhibition

H Guo, N Eleftheriadis, N Rohr-Udilova… - European Journal of …, 2017 - Elsevier
Abstract Human 15-lipoxygenase-1 (h-15-LOX-1) is a promising drug target in inflammation
and cancer. In this study substitution-oriented screening (SOS) has been used to identify …

[HTML][HTML] Chamaejasmin B decreases malignant characteristics of mouse melanoma B16F0 and B16F10 cells

L Si, X Yan, Y Wang, B Ren, H Ren, Y Ding… - Frontiers in …, 2020 - frontiersin.org
Chamaejasmin B (CHB), a natural biflavone isolated from Stellera chamaejasme L., has
been reported to exhibit anti-cancer properties; however, its effect in melanoma cells is not …

PDTX 模型在消化系统肿瘤研究中的应用进展# br## br

刘希敏, 胡守友, 陈玉根 - 临床肿瘤学杂志, 2018 - manu65.magtech.com.cn
人源性肿瘤组织异种移植(PDTX) 模型是通过将患者新鲜的肿瘤组织植入免疫缺陷小鼠,
依靠小鼠提供的微环境生长. 此模型保留了原代肿瘤的病理生理特性, 组织学和表型特征 …

TAK-733, a selective MEK inhibitor, enhances voreloxin-induced apoptosis in myeloid leukemia cells

E Jasek-Gajda, M Gajda, M Jasińska… - Anticancer …, 2018 - ar.iiarjournals.org
Background/Aim: MEK inhibitors are new promising anticancer drugs. The aim of this study
was to investigate the effect of the combination treatment of voreloxin with the MEK inhibitor …

[HTML][HTML] TAK-733 inhibits inflammatory neointimal formation by suppressing proliferation, migration, and inflammation in vitro and in vivo

JH Park, SW Kim, MJ Cha, N Yoon, CY Lee… - … & Molecular Medicine, 2018 - nature.com
As a potent and selective allosteric inhibitor of MEK, TAK-733 has been shown to exert anti-
cancer effects for a wide range of cancers both in vitro and in vivo. However, its effects on …

Evaluation of TAK-264, an antibody-drug conjugate in pancreatic cancer cell lines and patient-derived xenograft models

AR Schreiber, A Nguyen, SM Bagby… - Clinical cancer …, 2018 - ingentaconnect.com
Background: Antibody-drug conjugates (ADCs) are an emerging technology consisting of an
antibody, linker, and toxic agent, which have the potential to offer a targeted therapeutic …

TAK733 attenuates adrenergic receptor-mediated cardiomyocyte hypertrophy via inhibiting Erk Thr188 phosphorylation

CY Lee, J Lee, HH Seo, S Shin, SW Kim… - Clinical …, 2019 - content.iospress.com
BACKGROUND: Cardiac hypertrophy is an important risk factor for heart failure. The MEK-
ERK axis has been reported as a major regulator in controlling cardiac hypertrophy. TAK733 …