Antitumor activity of kinetochore-associated protein 2 siRNA against lung cancer patient-derived tumor xenografts
Author(s) -
Yukimasa Makita,
Mika Teratani,
Shumpei Murata,
Yasutaka Hoashi,
Satoru Matsumoto,
Yuji Kawamata
Publication year - 2018
Publication title -
oncology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.766
H-Index - 54
eISSN - 1792-1082
pISSN - 1792-1074
DOI - 10.3892/ol.2018.7890
Subject(s) - lung cancer , cancer research , oncogene , cancer , erlotinib , medicine , in vivo , gene knockdown , small interfering rna , molecular medicine , cell cycle , apoptosis , cell culture , biology , pathology , transfection , epidermal growth factor receptor , genetics , microbiology and biotechnology , biochemistry
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.
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