Potential Apoptotic Activities of Hylocereus undatus Peel and Pulp Extracts in MCF-7 and Caco-2 Cancer Cell Lines
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Date
2022-08
Journal Title
Journal ISSN
Volume Title
Type
Article
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Series Info
Plants;2022, 11, 2192.
Scientific Journal Rankings
Abstract
There is a huge demand for novel anticancer agents with fewer side effects compared to
current therapies. Pitaya, or dragon fruit, is a reservoir of potent anticancer compounds. This research
aimed to analyze the phytochemical components of Hylocereus undatus pulp and peel extracts using
LC-MS and GC-MS, and to investigate the in vitro effects of both extracts against cancer (breast,
MCF-7, and colon, Caco-2) and normal (lung; WI-38 and breast; MCF-10A) cell proliferation using
the MTT assay. The apoptosis potential of the anticancer effects was also evaluated using flow
cytometry, RT-PCR, and Western blot. The total phenolic and flavonoid contents in the peel extract
were significantly higher than those in the pulp extract. Compared to the flavonoid and phenolic acid
standards, the LC-MS analysis revealed the presence of nine compounds, which were represented
as 84.32 and 5.29 µg/g of the flavonoids and 686.11 and 148.72 µg/g of the phenolic acids in the
peel and pulp extracts, respectively. Among the identified compounds, chlorogenic acid, caffeic acid,
ferulic acid, and rutin were found at the highest concentration in both plant extracts. Both extracts
displayed cytotoxic activity against MCF-7 and Caco-2 cancer cells after 48 h of treatment at IC50
values ranging from 14 to 53 µg/mL with high selective indices against normal WI-38 and MCF-10A
cell lines. The increase in apoptosis was revealed by the overexpression of p53, BAX, and caspase-9
and the downregulation of antiapoptotic Bcl-2 mRNA and protein expressions. The results indicate
that H. undatus extracts can be a plant source for cancer therapy.
Description
Keywords
Hylocereus undatus, phenolic acids, flavonoids, pitaya, MCF-7, Caco-2, apoptosis, p53, Bcl-2 mRNA, anticancer