نتایج جستجو برای: multi cyclin dependentkinase inhibitors

تعداد نتایج: 670555  

2002
L. Michaels

6. Dolcetti R, Doglioni C, Maestro R et al. P53 over-expression is an early event in the development of human squamous-cell carcinoma of the larynx: Genetic and prognostic implications. Int J Cancer 1992; 52(2): 178-1 82. 7. Calitano J, van der Riet P, Westra W at al. Genetic progression model forhead and neck cancer: Implications for field cancerization. Cancer Res 1996; 56: 2488-2492. 8. El-D...

2016
Xianfeng Huang Yuanyuan Liu Cheng Zhang Guoqiang Song

s: A novel series of pyrazole derivatives containing hydroxamic acid group were designed and synthesized as multi-target inhibitors targeting CDK2 (cyclin-dependent kinases 2) and HDAC (histone deacetylase). Compounds 6e and 6f exhibited most potent CDK2 inhibition as well as HDAC inhibition. In vitro antiproliferative assay indicated that several compounds showed better antiproliferative poten...

Journal: :iranian journal of medical sciences 0
mohammad hasanzadeh_nazarabadi department of medical genetics, mashhad university of medical sciences, mashhad, iran tayebeh hamzehloie department of medical genetics, mashhad university of medical sciences, mashhad, iran majid mojarrad department of medical genetics, mashhad university of medical sciences, mashhad, iran sahar shekouhi department of medical genetics, mashhad university of medical sci-ences, mashhad, iran

the gene tp53 (also known as protein 53 or tumor protein 53), encoding transcription factor p53, is mutated or deleted in half of human cancers, demonstrating the crucial role of p53 in tumor suppression. there are reports of nearly 250 independent germ line tp53 mutations in over 100 publications. the p53 protein has the structure of a transcription factor and, is made up of several domains. t...

Journal: :Cell 2007
Isabel Chu Jun Sun Angel Arnaout Harriette Kahn Wedad Hanna Steven Narod Ping Sun Cheng-Keat Tan Ludger Hengst Joyce Slingerland

The kinase inhibitor p27Kip1 regulates the G1 cell cycle phase. Here, we present data indicating that the oncogenic kinase Src regulates p27 stability through phosphorylation of p27 at tyrosine 74 and tyrosine 88. Src inhibitors increase cellular p27 stability, and Src overexpression accelerates p27 proteolysis. Src-phosphorylated p27 is shown to inhibit cyclin E-Cdk2 poorly in vitro, and Src t...

Journal: :ESMO open 2023

Cyclin 4/6 inhibitors (CDKIs) are currently used in patients with hormone-dependent breast cancer as first-line treatment for metastatic disease. One of their less frequent but equally limiting adverse events is skin toxicity. The purpose the study was to report incidence toxicity treated CDKIs our center. Between November 2017 and December 2022, information from affected (MBC) at Hospital del ...

2012
FABRIZIO GALIMBERTI ALEXANDER M. BUSCH FADZAI CHINYENGETERE TIAN MA DAVID SEKULA VINCENT A. MEMOLI KONSTANTIN H. DRAGNEV FANG LIU KEVIN C. JOHNSON YONGLI GUO SARAH J. FREEMANTLE ANGELINE S. ANDREW PATRICIA GRENINGER DAVID J. ROBBINS JEFF SETTLEMAN CYRIL BENES ETHAN DMITROVSKY

Hedgehog (HH) pathway Smoothened (Smo) inhibitors are active against Gorlin syndrome-associated basal cell carcinoma (BCC) and medulloblastoma where Patched (Ptch) mutations occur. We interrogated 705 epithelial cancer cell lines for growth response to the Smo inhibitor cyclopamine and for expressed HH pathway-regulated species in a linked genetic...

2015
Satoshi Koyama Tomohiro Omura Atsushi Yonezawa Satoshi Imai Shunsaku Nakagawa Takayuki Nakagawa Ikuko Yano Kazuo Matsubara Pier Giorgio Petronini

Gefitinib and erlotinib are anticancer agents, which inhibit epidermal growth factor receptor (EGFR) tyrosine kinase. Interstitial lung disease (ILD) occurs in patients with non-small cell lung cancer receiving EGFR inhibitors. In the present study, we examined whether gefitinib- and erlotinib-induced lung injury related to ILD through endoplasmic reticulum (ER) stress, which is a causative int...

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