AXL-driven EMT state as a targetable conduit in cancer
The receptor tyrosine kinase (RTK) AXL has been intrinsically linked to epithelial–
mesenchymal transition (EMT) and promoting cell survival, anoikis resistance, invasion, and …
mesenchymal transition (EMT) and promoting cell survival, anoikis resistance, invasion, and …
The role of the receptor tyrosine kinase Axl in carcinogenesis and development of therapeutic resistance: An overview of molecular mechanisms and future …
Simple Summary The tyrosine kinase receptor Axl is an oncogene that promotes cancer
development by increasing proliferation, survival, invasion, and migration in cancer cells. Axl …
development by increasing proliferation, survival, invasion, and migration in cancer cells. Axl …
LFQ-analyst: an easy-to-use interactive web platform to analyze and visualize label-free proteomics data preprocessed with MaxQuant
Relative label-free quantification (LFQ) of shotgun proteomics data using precursor (MS1)
signal intensities is one of the most commonly used applications to comprehensively and …
signal intensities is one of the most commonly used applications to comprehensively and …
Cooperative targeting of melanoma heterogeneity with an AXL antibody-drug conjugate and BRAF/MEK inhibitors
J Boshuizen, LA Koopman, O Krijgsman, A Shahrabi… - Nature Medicine, 2018 - nature.com
Intratumor heterogeneity is a key factor contributing to therapeutic failure and, hence, cancer
lethality. Heterogeneous tumors show partial therapy responses, allowing for the emergence …
lethality. Heterogeneous tumors show partial therapy responses, allowing for the emergence …
AXL-a new player in resistance to HER2 blockade
HER2 is a driver in solid tumors, mainly breast, oesophageal and gastric cancer, through
activation of oncogenic signaling pathways such as PI3K or MAPK. HER2 overexpression …
activation of oncogenic signaling pathways such as PI3K or MAPK. HER2 overexpression …
Preclinical Characteristics of the Irreversible Pan-HER Kinase Inhibitor Neratinib Compared with Lapatinib: Implications for the Treatment of HER2-Positive and HER2 …
DM Collins, NT Conlon, S Kannan, CS Verma, LD Eli… - Cancers, 2019 - mdpi.com
An estimated 15–20% of breast cancers overexpress human epidermal growth factor
receptor 2 (HER2/ERBB2/neu). Two small-molecule tyrosine kinase inhibitors (TKIs) …
receptor 2 (HER2/ERBB2/neu). Two small-molecule tyrosine kinase inhibitors (TKIs) …
Novel therapies and strategies to overcome resistance to anti-HER2-targeted drugs
M Gámez-Chiachio, D Sarrió, G Moreno-Bueno - Cancers, 2022 - mdpi.com
Simple Summary Drug resistance is the “Achilles' heel” in current oncology. In this sense,
the clinical management of HER2 breast carcinomas (tumors with overexpression …
the clinical management of HER2 breast carcinomas (tumors with overexpression …
Roles of Grainyhead-like transcription factors in cancer
SM Frisch, JC Farris, PM Pifer - Oncogene, 2017 - nature.com
The mammalian homologs of the D. melanogaster Grainyhead gene, Grainyhead-like 1–3
(GRHL1, GRHL2 and GRHL3), are transcription factors implicated in wound healing …
(GRHL1, GRHL2 and GRHL3), are transcription factors implicated in wound healing …
Evolution of HER2-positive mammary carcinoma: HER2 loss reveals claudin-low traits in cancer progression
V Giusti, F Ruzzi, L Landuzzi, ML Ianzano, R Laranga… - Oncogenesis, 2021 - nature.com
HER2-positive breast cancers may lose HER2 expression in recurrences and metastases. In
this work, we studied cell lines derived from two transgenic mammary tumors driven by …
this work, we studied cell lines derived from two transgenic mammary tumors driven by …
Rapid discovery and structure–activity relationships of pyrazolopyrimidines that potently suppress breast cancer cell growth via SRC kinase inhibition with exceptional …
C Fraser, JC Dawson, R Dowling… - Journal of medicinal …, 2016 - ACS Publications
Novel pyrazolopyrimidines displaying high potency and selectivity toward SRC family
kinases have been developed by combining ligand-based design and phenotypic screening …
kinases have been developed by combining ligand-based design and phenotypic screening …