Targeting Heme Oxygenase 2 (HO2) with TiNIR, a Theragnostic Approach for Managing Metastatic Non-Small Cell Lung Cancer

Author:

Mun Seul-Ki12,Sim Hyun Bo1,Lee Jae-Hyuk3,Kim Hyeongyeong1,Park Dae-Han1,Lee Yong-An4,Han Ji Yeon1,Choi Yu-Jeong1,Son Jun Sang1,Park Jeongwon3,Lim Tae-Hwan2,Yee Sung-Tae2,Chang Young-Tae56,Lee Seongsoo378,Chang Dong-Jo2,Kim Jong-Jin1

Affiliation:

1. Department of Biomedical Science, Sunchon National University, Suncheon 57922, Republic of Korea.

2. College of Pharmacy and Research Institute of Life and Pharmaceutical Sciences, Sunchon National University, Suncheon 57922, Republic of Korea.

3. Gwangju Center, Korea Basic Science Institute (KBSI), Gwangju 61751, Republic of Korea.

4. Genome Institute of Singapore (GIS), Agency for Science, Technology and Research (A*STAR), 60 Biopolis Street, Genome, Singapore 138672, Republic of Singapore.

5. School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea.

6. Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea.

7. Department of Systems Biotechnology, Chung-Ang University, Anseong 17546, Republic of Korea.

8. Department of Bio-Analysis Science, University of Science & Technology, Daejeon 34113, Republic of Korea.

Abstract

Despite notable advancements in cancer therapeutics, metastasis remains a primary obstacle impeding a successful prognosis. Our prior study has identified heme oxygenase 2 (HO2) as a promising therapeutic biomarker for the aggressive subsets within tumor. This study aims to systematically evaluate HO2 as a therapeutic target of cancer, with a specific emphasis on its efficacy in addressing cancer metastasis. Through targeted inhibition of HO2 by TiNIR (tumor-initiating cell probe with near infrared), we observed a marked increase in reactive oxygen species. This, in turn, orchestrated the modulation of AKT and cJUN activation, culminating in a substantial attenuation of both proliferation and migration within a metastatic cancer cell model. Furthermore, in a mouse model, clear inhibition of cancer metastasis was unequivocally demonstrated with an HO2 inhibitor administration. These findings underscore the therapeutic promise of targeting HO2 as a strategic intervention to impede cancer metastasis, enhancing the effectiveness of cancer treatments.

Publisher

American Association for the Advancement of Science (AAAS)

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