IntAct—open source resource for molecular interaction data

…, J Khadake, C Leroy, A Liban, C Lieftink… - Nucleic acids …, 2007 - academic.oup.com
IntAct is an open source database and software suite for modeling, storing and analyzing
molecular interaction data. The data available in the database originates entirely from …

Reversible and adaptive resistance to BRAF (V600E) inhibition in melanoma

…, SM Willems, D Zecchin, S Hobor, PK Bajpe, C Lieftink… - Nature, 2014 - nature.com
Abstract Treatment of BRAF(V600E) mutant melanoma by small molecule drugs that target
the BRAF or MEK kinases can be effective, but resistance develops invariably 1 , 2 . In …

EGFR activation limits the response of liver cancer to lenvatinib

H Jin, Y Shi, Y Lv, S Yuan, CFA Ramirez, C Lieftink… - Nature, 2021 - nature.com
Hepatocellular carcinoma (HCC)—the most common form of liver cancer—is an aggressive
malignancy with few effective treatment options 1 . Lenvatinib is a small-molecule inhibitor of …

[PDF][PDF] Intrinsic resistance to MEK inhibition in KRAS mutant lung and colon cancer through transcriptional induction of ERBB3

…, EF Smit, E Thunnissen, P Halonen, C Lieftink… - Cell reports, 2014 - cell.com
There are no effective therapies for the ∼30% of human malignancies with mutant RAS
oncogenes. Using a kinome-centered synthetic lethality screen, we find that suppression of the …

[PDF][PDF] Neutrophils kill antibody-opsonized cancer cells by trogoptosis

…, P Verkuijlen, H Janssen, P Halonen, C Lieftink… - Cell reports, 2018 - cell.com
Destruction of cancer cells by therapeutic antibodies occurs, at least in part, through
antibody-dependent cellular cytotoxicity (ADCC), and this can be mediated by various Fc-receptor-…

Inducing and exploiting vulnerabilities for the treatment of liver cancer

C Wang, S Vegna, H Jin, B Benedict, C Lieftink… - Nature, 2019 - nature.com
Liver cancer remains difficult to treat, owing to a paucity of drugs that target critical dependencies
1 , 2 ; broad-spectrum kinase inhibitors such as sorafenib provide only a modest benefit …

SHP2 is required for growth of KRAS-mutant non-small-cell lung cancer in vivo

…, G Germano, A Bosma, P Krimpenfort, C Lieftink… - Nature medicine, 2018 - nature.com
RAS mutations are frequent in human cancer, especially in pancreatic, colorectal and non-small-cell
lung cancers (NSCLCs) 1 , 2 – 3 . Inhibition of the RAS oncoproteins has proven …

A powerful drug combination strategy targeting glutamine addiction for the treatment of human liver cancer

…, H Wu, A Bosma, F Jochems, N Isima, G Jin, C Lieftink… - Elife, 2020 - elifesciences.org
The dependency of cancer cells on glutamine may be exploited therapeutically as a new
strategy for treating cancers that lack druggable driver genes. Here we found that human liver …

[PDF][PDF] PTPN11 is a central node in intrinsic and acquired resistance to targeted cancer drugs

…, B Evers, L Vecchione, V Gambino, C Lieftink… - Cell reports, 2015 - cell.com
Most BRAF (V600E) mutant melanomas are sensitive to selective BRAF inhibitors, but
BRAF mutant colon cancers are intrinsically resistant to these drugs because of feedback …

[PDF][PDF] High-throughput functional genetic and compound screens identify targets for senescence induction in cancer

…, C Wang, JMF Neto, S Mainardi, B Evers, C Lieftink… - Cell reports, 2017 - cell.com
Senescence is a proliferation arrest that can result from a variety of stresses. Cancer cells
can also undergo senescence, but the stresses that provoke cancer cells to undergo …