Tumours with class 3 BRAF mutants are sensitive to the inhibition of activated RAS

Z Yao, R Yaeger, VS Rodrik-Outmezguine, A Tao… - Nature, 2017 - nature.com
Approximately 200 BRAF mutant alleles have been identified in human tumours. Activating
BRAF mutants cause feedback inhibition of GTP-bound RAS, are RAS-independent and …

[HTML][HTML] Ado-trastuzumab emtansine for patients with HER2-mutant lung cancers: results from a phase II basket trial

BT Li, R Shen, D Buonocore, ZT Olah, A Ni… - Journal of Clinical …, 2018 - ncbi.nlm.nih.gov
Purpose Human epidermal growth factor receptor 2 (HER2, ERBB2)–activating mutations
occur in 2% of lung cancers. We assessed the activity of ado-trastuzumab emtansine, a …

Prognostic and predictive impact of circulating tumor DNA in patients with advanced cancers treated with immune checkpoint blockade

QU Zhang, J Luo, S Wu, H Si, C Gao, W Xu… - Cancer discovery, 2020 - AACR
The utility of circulating tumor DNA (ctDNA) as a biomarker in patients with advanced
cancers receiving immunotherapy is uncertain. We therefore analyzed pretreatment (n= 978) …

Tissue factor/factor VIIa inhibitors block angiogenesis and tumor growth through a nonhemostatic mechanism

TA Hembrough, GM Swartz, A Papathanassiu… - Cancer research, 2003 - AACR
An association between cancer and thrombosis has been recognized for more than a
century. However, the manner by which tumor growth is regulated by coagulation in vivo …

Targeting wild-type KRAS-amplified gastroesophageal cancer through combined MEK and SHP2 inhibition

GS Wong, J Zhou, JB Liu, Z Wu, X Xu, T Li, D Xu… - Nature medicine, 2018 - nature.com
The role of KRAS, when activated through canonical mutations, has been well established in
cancer. Here we explore a secondary means of KRAS activation in cancer: focal high-level …

Therapeutic promise of proteinase-activated receptor-2 antagonism in joint inflammation

EB Kelso, JC Lockhart, T Hembrough, L Dunning… - … of Pharmacology and …, 2006 - ASPET
Biological therapies such as tumor necrosis factor-α inhibitors have advanced the treatment
of rheumatoid arthritis, but one-third of patients do not respond to such therapy. Furthermore …

An approach to suppress the evolution of resistance in BRAFV600E-mutant cancer

Y Xue, L Martelotto, T Baslan, A Vides, M Solomon… - Nature medicine, 2017 - nature.com
The principles that govern the evolution of tumors exposed to targeted therapy are poorly
understood. Here we modeled the selection and propagation of an amplification in the BRAF …

Pazopanib or methotrexate–vinblastine combination chemotherapy in adult patients with progressive desmoid tumours (DESMOPAZ): a non-comparative, randomised …

M Toulmonde, M Pulido, I Ray-Coquard… - The Lancet …, 2019 - thelancet.com
Background Desmoid tumours are locally aggressive tumours associated with substantial
morbidity. No systemic treatments are approved for this disease, with methotrexate …

ENMD-2076 is an orally active kinase inhibitor with antiangiogenic and antiproliferative mechanisms of action

GC Fletcher, RD Brokx, TA Denny… - Molecular cancer …, 2011 - AACR
ENMD-2076 is a novel orally active, small molecule kinase inhibitor with a mechanism of
action involving several pathways key to tumor growth and survival: angiogenesis …

[PDF][PDF] Cytokeratin 8 functions as a major plasminogen receptor in select epithelial and carcinoma cells

SL Gonias, TA Hembrough, M Sankovic - Front Biosci, 2001 - article.imrpress.com
[Frontiers in Bioscience 6, d1403-1411, November 1, 2001] 1403 CYTOKERATIN 8
FUNCTIONS AS A MAJOR PLASMINOGEN RECEPTOR IN SELECT Page 1 [Frontiers in …