Isojamaicin, one of the isoflavonoids from Millettia griffoniana Baill (Fabaceae) has anticancer effect on human prostate cancer cells
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Jordan Lembe Tonga
and Derek Tantoh Ndinteh
Abstract
Objectives
The incidence of cancer, a second leading cause of death globally, continues to rise steadily, and could reach 28.4 million cases by 2040, if no action is taken. Prostate cancer, the second most common cancer in men globally following lung cancer, accounted for 1,414,259 new cases and led to 375,304 deaths in 2022. Chemotherapy and surgery remain the major treatments however, they are associated with side effects. In this study, the anticancer potentials of ten (10) isoflavonoids from Millettia griffoniana Bail was explored.
Methods
Anti-cell growth (MTT), proliferative (CCK-8) and clonogenic effects of these isoflavonoids were investigated. Furthermore, the most potent compound (isojamaicin) was investigated for its potential to induce apoptosis, inhibit cell migration/invasion and cell adhesion.
Results
Out of the 10 isoflavonoids isolated from M. griffoniana, isojamaicin significantly inhibited PC3 and LNCaP cell growth and proliferation in a concentration dependent manner. It also significantly (p<0.001) inhibited PC3 cell clone formation. It induced a potent (near 40 %) increment of apoptotic cell population in PC3 cells at both 30 and 60 μg/mL; which was followed by a notable increase in caspase-3 activity. Isojamaicin induced potent inhibition of PC3 cell invasion/migration and increased adhesion of PC3 cells to the extracellular matrix (collagen).
Conclusions
This study provides an unprecedented report of the anti-prostate cancer potential of isojamaicin and its possible underlying mechanisms. It merits further in vivo research to support the in vitro findings.
Funding source: Organisation for the Prohibition of Chemical Weapons
Award Identifier / Grant number: OPCW 188/22 1/3 INS
Acknowledgments
This study received support from the OPCW (Organization for the Prohibition of Chemical Weapons) under Grant No. OPCW 188/22 1/3 INS, awarded to Prof. Dr. Stephane Zingue.
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Research ethics: Not applicable.
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Informed consent: Not applicable.
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Author contributions: NDT, ZS, MME, YE and ND designed the experiments. TLJ, KKHM, RNR, TFM, YE and NDT performed the phytochemistry part of this work. ZS and ND performed the in vitro experiments. TLJ, KKHM and ZS analyzed the data. TLJ, KKHM and ZS wrote the paper and all authors read and approved the manuscript.
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Use of Large Language Models, AI and Machine Learning Tools: None declared.
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Conflict of interest: The authors declare no conflict of interest.
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Research funding: Prof. Dr. Stephane Zingue was Granted OPCW (reference # OPCW 188/22 1/3 INS).
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Availability of data and materials: The data and materials utilized in this study are accessible upon request from the authors.
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Consent for publication: All authors consent the publication of this manuscript on this journal.
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