Ibulocydine Inhibits Migration and Invasion of TNBC Cells via MMP-9 Regulation

Author:

Kwon Mi-Ri123,Park Ji-Soo4,Ko Eun-Jung23,Park Jin23,Ju Eun-Jin23,Shin Seol-Hwa23,Son Ga-Won123,Lee Hye-Won123,Park Yun-Yong5ORCID,Kang Myoung-Hee2ORCID,Kim Yeon-Joo6,Kim Byeong-Moon4ORCID,Lee Hee-Jin7,Kim Tae-Won38,Kim Chong-Jai37,Song Si-Yeol36,Park Seok-Soon23ORCID,Jeong Seong-Yun1239

Affiliation:

1. Department of Medical Science, Asan Medical Institute of Convergence Science and Technology, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea

2. Asan Institute for Life Sciences, Asan Medical Center, Seoul 05505, Republic of Korea

3. Asan Preclinical Evaluation Center for Cancer Therapeutix, Asan Medical Center, Seoul 05505, Republic of Korea

4. Department of Chemistry, Seoul National University, Seoul 08826, Republic of Korea

5. Department of Life Science, Chung-Ang University, Seoul 06974, Republic of Korea

6. Department of Radiation Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea

7. Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea

8. Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea

9. Department of Biochemistry and Molecular Biology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea

Abstract

Triple-negative breast cancer (TNBC) accounts for approximately 15–20% of all breast cancer types, indicating a poor survival prognosis with a more aggressive biology of metastasis to the lung and a short response duration to available therapies. Ibulocydine (IB) is a novel (cyclin-dependent kinase) CDK7/9 inhibitor prodrug displaying potent anti-cancer effects against various cancer cell types. We performed in vitro and in vivo experiments to determine whether IB inhibits metastasis and eventually overcomes the poor drug response in TNBC. The result showed that IB inhibited the growth of TNBC cells by inducing caspase-mediated apoptosis and blocking metastasis by reducing MMP-9 expression in vitro. Concurrently, in vivo experiments using the metastasis model showed that IB inhibited metastasis of MDA-MB-231-Luc cells to the lung. Collectively, these results demonstrate that IB inhibited the growth of TNBC cells and blocked metastasis by regulating MMP-9 expression, suggesting a novel therapeutic agent for metastatic TNBC.

Funder

Korea Health Technology R&D Project through the Korea Health Industry Development Institute

National Research Foundation of Korea

Bio&Medical Technology Development Program of the National Research Foundation

Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea

Publisher

MDPI AG

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