| Literature DB >> 29541240 |
Yukimasa Makita1, Mika Teratani1, Shumpei Murata1, Yasutaka Hoashi1, Satoru Matsumoto1, Yuji Kawamata1.
Abstract
It has been widely reported that patient-derived tumor xenografts (PDXs) are more similar to tumor tissues than conventional cancer cell lines. Kinetochore-associated protein 2 (KNTC2) is known to be upregulated specifically in tumor tissues of cancer patients and is recognized as a potential target for cancer therapy. Previously, in vivo antitumor activities of KNTC2 short interfering RNA encapsulated into a lipid nanoparticle (KNTC2-LNP) were reported in orthotopic hepatocellular carcinoma mouse models. However, it remains unclear whether KNTC2-LNP exhibits antitumor activities against lung cancer PDXs. In the present study, the antitumor activities of KNTC2-LNP were clarified in a three-dimensional culture system and a subcutaneous tumor model of lung cancer PDX, LC-60, which was resistant to erlotinib. Growth inhibitory activities of KNTC2-LNP were associated with knockdown activities. Furthermore, KNTC2-LNP also exhibited in vivo antitumor activity against another lung cancer PDX, LC-45, which was sensitive to erlotinib. These results suggest that KNTC2 is a promising target for patients with lung cancer.Entities:
Keywords: erlotinib; kinetochore-associated protein 2; lipid nanoparticle; lung cancer; patient-derived tumor xenograft; short interfering RNA; three-dimensional culture
Year: 2018 PMID: 29541240 PMCID: PMC5835869 DOI: 10.3892/ol.2018.7890
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967