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Article

Antitumor Activity of a Novel Tyrosine Kinase Inhibitor AIU2001 Due to Abrogation of the DNA Damage Repair in Non-Small Cell Lung Cancer Cells

1
Division of Radiation Biomedical Research, Korea Institute of Radiological & Medical Sciences (KIRAMS), Seoul 01812, Korea
2
Department of Biology, Korea University, Seoul 02841, Korea
3
Department of Medicinal Chemistry, Jungwon University, Goesan 28024, Korea
*
Author to whom correspondence should be addressed.
Both of the authors are listed as co-first authors and contributed equally to this work.
Int. J. Mol. Sci. 2019, 20(19), 4728; https://doi.org/10.3390/ijms20194728
Received: 2 September 2019 / Revised: 21 September 2019 / Accepted: 23 September 2019 / Published: 24 September 2019
(This article belongs to the Section Molecular Pathology, Diagnostics, and Therapeutics)
Class III receptor tyrosine kinase (RTK) inhibitors targeting mainly FLT3 or c-KIT have not been well studied in lung cancer. To identify a small molecule potentially targeting class III RTK, we synthesized novel small molecule compounds and identified 5-(4-bromophenyl)-N-(naphthalen-1-yl) oxazol-2-amine (AIU2001) as a novel class III RKT inhibitor. In an in vitro kinase profiling assay, AIU2001 inhibited the activities of FLT3, mutated FLT3, FLT4, and c-KIT of class III RTK, and the proliferation of NSCLC cells in vitro and in vivo. AIU2001 induced DNA damage, reactive oxygen species (ROS) generation, and cell cycle arrest in the G2/M phase. Furthermore, AIU2001 suppressed the DNA damage repair genes, resulting in the ‘BRCAness’/‘DNA-PKness’ phenotype. The mRNA expression level of STAT5 was downregulated by AIU2001 treatment and knockdown of STAT5 inhibited the DNA repair genes. Our results show that compared to either drug alone, the combination of AIU2001 with a poly (ADP-ribose) polymerase (PARP) inhibitor olaparib or irradiation showed synergistic efficacy in H1299 and A549 cells. Hence, our findings demonstrate that AIU2001 is a candidate therapeutic agent for NSCLC and combination therapies with AIU2001 and a PARP inhibitor or radiotherapy may be used to increase the therapeutic efficacy of AIU2001 due to inhibition of DNA damage repair. View Full-Text
Keywords: FLT3 inhibitor; Class III RTK; NSCLC; apoptosis; cell cycle arrest; DNA damage repair; PARP-1 inhibitor FLT3 inhibitor; Class III RTK; NSCLC; apoptosis; cell cycle arrest; DNA damage repair; PARP-1 inhibitor
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MDPI and ACS Style

Ryu, H.; Choi, H.-K.; Kim, H.J.; Kim, A.-Y.; Song, J.-Y.; Hwang, S.-G.; Kim, J.-S.; Kim, D.-U.; Kim, E.-H.; Kim, J.; Ahn, J. Antitumor Activity of a Novel Tyrosine Kinase Inhibitor AIU2001 Due to Abrogation of the DNA Damage Repair in Non-Small Cell Lung Cancer Cells. Int. J. Mol. Sci. 2019, 20, 4728. https://doi.org/10.3390/ijms20194728

AMA Style

Ryu H, Choi H-K, Kim HJ, Kim A-Y, Song J-Y, Hwang S-G, Kim J-S, Kim D-U, Kim E-H, Kim J, Ahn J. Antitumor Activity of a Novel Tyrosine Kinase Inhibitor AIU2001 Due to Abrogation of the DNA Damage Repair in Non-Small Cell Lung Cancer Cells. International Journal of Molecular Sciences. 2019; 20(19):4728. https://doi.org/10.3390/ijms20194728

Chicago/Turabian Style

Ryu, Hwani, Hyun-Kyung Choi, Hyo J. Kim, Ah-Young Kim, Jie-Young Song, Sang-Gu Hwang, Jae-Sung Kim, Da-Un Kim, Eun-Ho Kim, Joon Kim, and Jiyeon Ahn. 2019. "Antitumor Activity of a Novel Tyrosine Kinase Inhibitor AIU2001 Due to Abrogation of the DNA Damage Repair in Non-Small Cell Lung Cancer Cells" International Journal of Molecular Sciences 20, no. 19: 4728. https://doi.org/10.3390/ijms20194728

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