A microRNA component of the p53 tumour suppressor network
A global decrease in microRNA (miRNA) levels is often observed in human cancers 1 , 2 ,
indicating that small RNAs may have an intrinsic function in tumour suppression. To identify …
indicating that small RNAs may have an intrinsic function in tumour suppression. To identify …
The gene encoding the splicing factor SF2/ASF is a proto-oncogene
R Karni, E de Stanchina, SW Lowe, R Sinha… - Nature structural & …, 2007 - nature.com
Alternative splicing modulates the expression of many oncogene and tumor-suppressor
isoforms. We have tested whether some alternative splicing factors are involved in cancer. We …
isoforms. We have tested whether some alternative splicing factors are involved in cancer. We …
E1A signaling to p53 involves the p19ARFtumor suppressor
E de Stanchina, ME McCurrach, F Zindy… - Genes & …, 1998 - genesdev.cshlp.org
The adenovirus E1A oncogene activates p53 through a signaling pathway involving the
retinoblastoma protein and the tumor suppressor p19 ARF . The ability of E1A to induce p53 and …
retinoblastoma protein and the tumor suppressor p19 ARF . The ability of E1A to induce p53 and …
SOX2 promotes lineage plasticity and antiandrogen resistance in TP53- and RB1-deficient prostate cancer
Some cancers evade targeted therapies through a mechanism known as lineage plasticity,
whereby tumor cells acquire phenotypic characteristics of a cell lineage whose survival no …
whereby tumor cells acquire phenotypic characteristics of a cell lineage whose survival no …
Hypoxic and Ras-transformed cells support growth by scavenging unsaturated fatty acids from lysophospholipids
… In addition, we find that hypoxic cells bypass de novo lipogenesis, and thus, both the need
for … Hypoxic reprogramming of de novo lipogenesis can be reproduced in normoxic cells by …
for … Hypoxic reprogramming of de novo lipogenesis can be reproduced in normoxic cells by …
ARN-509: a novel antiandrogen for prostate cancer treatment
…, P Smith-Jones, M Klang, ND Smith, E De Stanchina… - Cancer research, 2012 - AACR
Continued reliance on the androgen receptor (AR) is now understood as a core mechanism
in castration-resistant prostate cancer (CRPC), the most advanced form of this disease. …
in castration-resistant prostate cancer (CRPC), the most advanced form of this disease. …
The regulation of AMPK β1, TSC2, and PTEN expression by p53: stress, cell and tissue specificity, and the role of these gene products in modulating the IGF-1-AKT …
Z Feng, W Hu, E De Stanchina, AK Teresky, S Jin… - Cancer research, 2007 - AACR
The insulin-like growth factor 1 (IGF-1)-AKT-mTOR pathways sense the availability of nutrients
and mitogens and respond by signaling for cell growth and division. The p53 pathway …
and mitogens and respond by signaling for cell growth and division. The p53 pathway …
HER2 Amplification: A Potential Mechanism of Acquired Resistance to EGFR Inhibition in EGFR-Mutant Lung Cancers That Lack the Second-Site EGFRT790M …
…, ME Arcila, CA Nebhan, X Song, E de Stanchina… - Cancer discovery, 2012 - AACR
EGF receptor (EGFR)–mutant lung cancers eventually become resistant to treatment with
EGFR tyrosine kinase inhibitors (TKI). The combination of EGFR-TKI afatinib and anti-EGFR …
EGFR tyrosine kinase inhibitors (TKI). The combination of EGFR-TKI afatinib and anti-EGFR …
[PDF][PDF] Metastatic latency and immune evasion through autocrine inhibition of WNT
Metastasis frequently develops years after the removal of a primary tumor, from a minority of
disseminated cancer cells that survived as latent entities through unknown mechanisms. We …
disseminated cancer cells that survived as latent entities through unknown mechanisms. We …
In vivo engineering of oncogenic chromosomal rearrangements with the CRISPR/Cas9 system
…, P Ogrodowski, A Crippa, N Rekhtman, E de Stanchina… - Nature, 2014 - nature.com
Chromosomal rearrangements have a central role in the pathogenesis of human cancers
and often result in the expression of therapeutically actionable gene fusions 1 . A recently …
and often result in the expression of therapeutically actionable gene fusions 1 . A recently …