| Literature DB >> 28966993 |
Abstract
Large-scale screening has revealed that human hematopoietic cancer cell lines are generally more sensitive to various classes of drugs than cell lines established from solid tumors. A detailed examination of data in the Cancer Therapeutics Response Portal (http://portals.broadinstitute.org/ctrp/) suggests that this enhanced sensitivity is due to lower basal levels of activation of TAZ-TEAD mechanotransduction pathways in hematopoietic versus non-hematopoietic cells. Translation inhibitors such as omacetaxine mepesuccinate (homoharringtonine) fall into this category of hematopoietic-selective compounds. Moreover, additional molecular determinants of sensitivity suggest that homoharringtonine might show therapeutic efficacy in certain patients with advanced hematologic malignancies despite activation of these pathways.Entities:
Keywords: Omacetaxine mepesuccinate (homoharringtonine); RPL3; TAZ-TEAD; TNFRSF12A
Year: 2017 PMID: 28966993 PMCID: PMC5617356 DOI: 10.14218/ERHM.2017.00022
Source DB: PubMed Journal: Explor Res Hypothesis Med ISSN: 2472-0712