MassIVE MSV000088681

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The proteomic landscape of ovarian cancer cells in response to melatonin

Description

Ovarian cancer (OC) is the most lethal gynecological malignancy with a highly negative prognosis. Melatonin is an indoleamine secreted by the pineal gland during darkness and has shown antitumor activity in both in vitro and in vivo experiments. Herein, we investigated the influence of melatonin on the proteome of human ovarian carcinoma cells (SKOV-3 cell line) using the Ultimate 3000 LC Liquid NanoChromatography equipment coupled to a Q-Exactive mass spectrometry. After 48 h of treatment, melatonin induced a significant cytotoxicity especially with the highest melatonin concentration. The proteomic profile revealed 639 proteins in the control group, and 98, 110, and 128 proteins were altered by melatonin at the doses of 0.8, 1.6, and 2.4 mM, respectively. Proteins associated with the immune system and tricarboxylic acid cycle were increased in the three melatonin-exposed groups of cells. Specifically, the dose of 2.4 mM led to a reduction in molecules associated with protein synthesis, especially those of the ribosomal protein family. We also identified 28 potential genes shared between normal ovarian tissue and OC in all experimental groups, and melatonin was predicted to alter genes encoding ribosomal proteins. Notably, the set of proteins changed by melatonin was linked to a better prognosis for OC patients. We conclude that melatonin significantly alters the proteome of SKOV-3 cells by changing proteins involved with the immune response and mitochondrial metabolism. The concentration of 2.4 mM of melatonin promoted the largest number of protein changes. The evidence suggests that melatonin may be an effective therapeutic strategy against OC. [doi:10.25345/C5BW1Z] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Ovarian cancer ; Melatonin ; SKOV-3 cell line ; Proteomic Analysis

Contact

Principal Investigators:
(in alphabetical order)
Lucilene Delazari dos Santos, Biotechnology Institute (IBTEC)/UNESP, Botucatu, SP, Brasil
Luiz Gustavo de Almeida Chuffa, Department of Structural and Functional Biology, Institute of Biosciences, UNESP, Botucatu, SP, Brazil
Roberta Carvalho Cesario, Department of Structural and Functional Biology, Institute of Biosciences, UNESP, Botucatu, SP, Brazil
Submitting User: lucilene
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