Mechanism of cis-Nerolidol-Induced Bladder Carcinoma Cell Death

Author:

Glumac Mateo1,Čikeš Čulić Vedrana2ORCID,Marinović-Terzić Ivana1ORCID,Radan Mila3ORCID

Affiliation:

1. Department of Immunology and Medical Genetics, School of Medicine, University of Split, 21000 Split, Croatia

2. Department of Medicinal Chemistry and Biochemistry, School of Medicine, University of Split, 21000 Split, Croatia

3. Department of Biochemistry, Faculty of Chemistry and Technology, University of Split, 21000 Split, Croatia

Abstract

Nerolidol is a naturally occurring sesquiterpene alcohol with multiple properties, including antioxidant, antibacterial, and antiparasitic activities. A few studies investigating the antitumor properties of nerolidol have shown positive results in both cell culture and mouse models. In this study, we investigated the antitumor mechanism of cis-nerolidol in bladder carcinoma cell lines. The results of our experiments on two bladder carcinoma cell lines revealed that nerolidol inhibited cell proliferation and induced two distinct cell death pathways. We confirmed that cis-nerolidol induces DNA damage and ER stress. A mechanistic study identified a common cAMP, Ca2+, and MAPK axis involved in signal propagation and amplification, leading to ER stress. Inhibition of any part of this signaling cascade prevented both cell death pathways. The two cell death mechanisms can be distinguished by the involvement of caspases. The early occurring cell death pathway is characterized by membrane blebbing and cell swelling followed by membrane rupture, which can be prevented by the inhibition of caspase activation. In the late cell death pathway, which was found to be caspase-independent, cytoplasmic vacuolization and changes in cell shape were observed. cis-Nerolidol shows promising antitumor activity through an unorthodox mechanism of action that could help target resistant forms of malignancies, such as bladder cancer.

Funder

Croatian Science Foundation

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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