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10.2147/BCTT.S54414

http://scihub22266oqcxt.onion/10.2147/BCTT.S54414
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C4467661!4467661!26089701
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suck abstract from ncbi


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pmid26089701      Breast+Cancer+(Dove+Med+Press) 2015 ; 7 (ä): 147-62
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  • Profile of neratinib and its potential in the treatment of breast cancer #MMPMID26089701
  • Feldinger K; Kong A
  • Breast Cancer (Dove Med Press) 2015[]; 7 (ä): 147-62 PMID26089701show ga
  • The HER (ErbB) receptor tyrosine kinase receptors are implicated in many cancers and several anti-HER treatments are now approved. In recent years, a new group of compounds that bind irreversibly to the adenosine triphosphate binding pocket of HER receptors have been developed. One of these compounds, neratinib, has passed preclinical phases and is currently undergoing various clinical trials. This manuscript reviews the preclinical as well as clinical data on neratinib. As a pan-HER inhibitor, this irreversible tyrosine kinase inhibitor binds and inhibits the tyrosine kinase activity of epidermal growth factor receptors, EGFR (or HER1), HER2 and HER4, which leads to reduced phosphorylation and activation of downstream signaling pathways. Neratinib has been shown to be effective against HER2-overexpressing or mutant tumors in vitro and in vivo. Neratinib is currently being investigated in various clinical trials in breast cancers and other solid tumors, including those with HER2 mutation. Earlier studies have already shown promising clinical activity for neratinib. However, more translational research is required to investigate biomarkers that could help to predict response and resistance for selection of appropriate patients for treatment with neratinib, either as monotherapy or in combination with other drug(s).
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