نتایج جستجو برای: ras oncogene

تعداد نتایج: 70453  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Rocky Cipriano Charlene E Kan James Graham David Danielpour Martha Stampfer Mark W Jackson

Oncogene-induced senescence (OIS), the proliferative arrest engaged in response to persistent oncogene activation, serves as an important tumor-suppressive barrier. We show here that finite lifespan human mammary epithelial cells (HMEC) undergo a p16/RB- and p53-independent OIS in response to oncogenic RAS that requires TGF-β signaling. Suppression of TGF-β signaling by expression of a dominant...

2012
Katherine M. Hannan Richard B. Pearson

The global effort to understand the molecular drivers of cancer onset and progression is now coming to fruition with the identification of specific genomic and epigenomic events that influence signaling through key oncogenic pathways. Genetic studies using inducible expression of the critical growth controlling oncogenes MYC, RAS, PI3K and AKT have shown unequivocally that, in conjunction with ...

Journal: :Cancer research 1987
P E Kiefer G Bepler M Kubasch K Havemann

Amplification and expression of 16 protooncogenes were examined in 12 established small cell lung cancer (SCLC) cell lines. Seven of 12 cell lines showed a 20- to 35-fold amplification of the c-myc oncogene, 3 cell lines showed an 80- to 130-fold amplification of N-myc oncogene, and one cell line had a simultaneous amplification of the c-myb and N-myc oncogene. In this cell line both oncogenes ...

Journal: :Indian Journal of Medical and Paediatric Oncology 2023

In resource-constraint settings, genetic testing is rarely available for patients. We report the association of SETBP1, a major oncogene interest in myeloid malignancies, with juvenile myelomonocytic leukemia (JMML) and GATA 1 mutation. The modulating role SETBP1 Rat sarcoma virus (RAS)-driven especially JMML, unknown. vivo vitro studies point to aggressive leukemogenesis.[1] mutation not consi...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1990
Y Yamaguchi-Iwai M Satake Y Murakami M Sakai M Muramatsu Y Ito

The activated c-Ha-ras oncogene induced AP1-site DNA-binding activity in F9 cells. This induction appeared to be due, at least in part, to the induction of c-jun transcription. Both activated c-Ha-ras and c-jun induced the differentiation of F9 cells to endoderm-like cells. Thus, AP1 appears to play a key role in the initial stage of F9 cell differentiation.

2016
Xiaonan Liu Wenchao Zhang Hua Guo Jiuling Yue Shanshan Zhuo

PURPOSE miR-98, a member of the let-7 family of microRNAs, is downregulated in many malignant tumors and has been correlated with tumor progression. However, the roles of miR-98 in salivary adenoid cystic carcinomas (SACCs) are still unclear. Thus, we explored the role of miR-98 in the pathogenesis of SACCs. METHODS Reverse transcription-polymerase chain reaction was used to quantify miR-98 e...

Journal: :Cancer research 1993
M Hofmann W Rudy U Günthert S G Zimmer V Zawadzki M Zöller R B Lichtner P Herrlich H Ponta

The activated oncogene c-Ha-ras induces expression of the surface glycoprotein CD44 in cloned rat embryonic fibroblasts (CREF). Induction is transcriptional as shown by transient cotransfections of c-Ha-ras expression constructs and CD44 promoter reporter gene constructs and depends on the presence of an AP-1 binding site at position -110. Increased transcript levels for the standard isoform of...

1997
Richard L. Darley Terence G. Hoy Paul Baines Rose Ann Padua Alan K. Burnett

RAS mutations arise at high frequency (20–40%) in both acute myeloid leukemia and myelodysplastic syndrome (which is considered to be a manifestation of preleukemic disease). In each case, mutations arise predominantly at the N-RAS locus. These observations suggest a fundamental role for this oncogene in leukemogenesis. However, despite its obvious significance, little is known of how this key ...

Journal: :Proceedings of the National Academy of Sciences 1988

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