Antitumor activity of α‐pinene in T‐cell tumors

Author:

Abe Masaya1,Asada Noboru2ORCID,Kimura Maiko1,Fukui Chie3,Yamada Daisuke4,Wang Ziyi5,Miyake Masayuki6,Takarada Takeshi4,Ono Mitsuaki5,Aoe Michinori6,Kitamura Wataru1,Matsuda Masayuki1,Moriyama Takashi1,Matsumura Akifumi1,Maeda Yoshinobu1

Affiliation:

1. Department of Hematology, Oncology and Respiratory Medicine Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan

2. Department of Hematology and Oncology Okayama University Hospital Okayama Japan

3. Division of Hematology, Department of Medicine Kobe University Hospital Kobe Japan

4. Department of Regenerative Science Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan

5. Department of Molecular Biology and Biochemistry Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan

6. Division of Medical Support Okayama University Hospital Okayama Japan

Abstract

AbstractT‐cell acute leukemia and lymphoma have a poor prognosis. Although new therapeutic agents have been developed, their therapeutic effects are suboptimal. α‐Pinene, a monoterpene compound, has an antitumor effect on solid tumors; however, few comprehensive investigations have been conducted on its impact on hematologic malignancies. This report provides a comprehensive analysis of the potential benefits of using α‐pinene as an antitumor agent for the treatment of T‐cell tumors. We found that α‐pinene inhibited the proliferation of hematologic malignancies, especially in T‐cell tumor cell lines EL‐4 and Molt‐4, induced mitochondrial dysfunction and reactive oxygen species accumulation, and inhibited NF‐κB p65 translocation into the nucleus, leading to robust apoptosis in EL‐4 cells. Collectively, these findings suggest that α‐pinene has potential as a therapeutic agent for T‐cell malignancies, and further investigation is warranted.

Funder

Wesco Science Foundation

Publisher

Wiley

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