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In Vitro Cytotoxic Activity and Phytochemical Characterization (UPLC/T-TOF-MS/MS) of the Watermelon ( Citrullus lanatus ) Rind Extract

Reusing food waste is becoming popular in pharmaceutical industries. Watermelon ( ) rind is commonly discarded as a major solid waste. Here, the in vitro cytotoxic potential of watermelon rind extracts was screened against a panel of human cancer cell lines. Cell cycle analysis was used to determine...

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Published in:Molecules (Basel, Switzerland) Switzerland), 2022-04, Vol.27 (8), p.2480
Main Authors: El Gizawy, Heba A, El-Haddad, Alaadin E, Attia, Yasmin M, Fahim, Sally A, Zafer, Mai M, Saadeldeen, Amr M
Format: Article
Language:English
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Summary:Reusing food waste is becoming popular in pharmaceutical industries. Watermelon ( ) rind is commonly discarded as a major solid waste. Here, the in vitro cytotoxic potential of watermelon rind extracts was screened against a panel of human cancer cell lines. Cell cycle analysis was used to determine the induction of cell death, whereas annexin V-FITC binding, caspase-3, BAX, and BCL-2 mRNA expression levels were used to determine the degree of apoptosis. VEGF-promoting angiogenesis and cell migration were also evaluated. Moreover, the identification of phytoconstituents in the rind extract was achieved using UPLC/T-TOF-MS/MS, and a total of 45 bioactive compounds were detected, including phenolic acids, flavonoids aglycones, and their glycoside derivatives. The tested watermelon rind extracts suppressed cell proliferation in seven cancer cell lines in a concentration-dependent manner. The cytotoxicity of the rind aqueous extract (RAE) was higher compared with that of the other extracts. In addition to a substantial inhibitory effect on cell migration, the RAE triggered apoptosis in HCT116 and Hep2 cells by driving the accumulation of cells in the S phase and elevating the activity of caspase-3 and the BAX/BCL-2 ratio. Thus, a complete phytochemical and cytotoxic investigation of the rind extract may identify its potential potency as an anticancer agent.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules27082480