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The CTD² Network and Cancer Systems Biology Consortium organized a virtual symposium series titled “Multidisciplinary Approaches to Understand Cancer Treatment Resistance”. Please join us on 11/16, 11/17, 12/2, 12/16, and 12/17. Click here to view the registration website.

Publications

644 Publications Available
Journal of Translational Medicine

Researchers identify Hepatocyte growth factor dependent signature may serve as a candidate predictive signature for patient enrollment in clinical trials using MET inhibitors.

Oncotarget

Researchers find that activation of EGFR signaling leads to resistance of BRAF inhibitors, and that adding EGFR inhibitors increases the efficacy of BRAF inhibitor treatment.

eLife

Researchers used a next-generation shRNA platform to screen for genes conferring resistance to carfilzomib in multiple myeloma cells.

PNAS

Researcehrs describe the discovery of the small-molecule probe BRD5631, and demonstrate that BRD5631 affects several cellular disease phenotypes previously linked to autophagy.

Cell

 The authors analyzed cellular perturbation profiles to identify established MoA proteins for 70% of tested compounds.

Cancer Research

Researchers find that RAS pathway activation can act as a biomarker for sensitivity of ovarian cancer cells to decitabine.

Cell

Researchers report mTORC1 activation suppresses proliferation when cells rely on extracellular proteins as an amino acid source, and these results may have important implications for the use of mTOR inhibitors as therapeutics.

Proceedings of the National Academy of Sciences in the United State of America

Researchers optimize several aspects of shRNA libraries to create next-generation high-complexity mouse and human shRNA libraries.

Cell

Researcehrs show human colorectal cancers (CRC)cells can revert to functioning normal cells given appropriate signals and provide compelling in vivo validation of the Wnt pathway as a therapeutic target for treatment of CRC.

Nature Communication

Researchers introduce a cell culture medium that enables routine establishment of cell lines from human ovarian cancers which retain the genomic landscape, histopathology and molecular features of the original tumours.