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Chemical Constituents of Callistemon subulatus and Their Anti-Pancreatic Cancer Activity against Human PANC-1 Cell Line.


ABSTRACT: An n-hexane extract of Callistemon subulatus was found to exhibit potent cytotoxicity against PANC-1 human pancreatic cancer cells, preferentially under nutrition starvation conditions, with a PC50 value of 6.2 µg/mL. Phytochemical investigation of this bioactive extract resulted in the isolation of fifteen compounds (1-15), including a new compound, subulatone A (-). The structure of compound 1 was elucidated using HRFABMS and NMR spectroscopic analyses. The isolated compounds were tested for their preferential cytotoxicity against the PANC-1 human pancreatic cancer cell line, using an anti-austerity strategy. Among these, myrtucommulone A (2) showed highly potent preferential cytotoxicity, with a PC50 value of 0.28 µM. Myrtucommulone A (2) was found to alter PANC-1 cell morphology, inhibit cell migration, and downregulate the PI3K/Akt/mTOR and autophagy signaling pathways in nutrient-deprived media, leading to cancer cell death. Therefore, myrtucommulone A (2) is a lead compound for anticancer drug development based on an anti-austerity strategy.

SUBMITTER: Maneenet J 

PROVIDER: S-EPMC9570665 | biostudies-literature | 2022 Sep

REPOSITORIES: biostudies-literature

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Chemical Constituents of <i>Callistemon subulatus</i> and Their Anti-Pancreatic Cancer Activity against Human PANC-1 Cell Line.

Maneenet Juthamart J   Tawila Ahmed M AM   Omar Ashraf M AM   Phan Nguyen Duy ND   Ojima Chiharu C   Kuroda Masahiro M   Sato Mao M   Mizoguchi Mio M   Takahashi Ikue I   Awale Suresh S  

Plants (Basel, Switzerland) 20220921 19


An n-hexane extract of <i>Callistemon subulatus</i> was found to exhibit potent cytotoxicity against PANC-1 human pancreatic cancer cells, preferentially under nutrition starvation conditions, with a PC<sub>50</sub> value of 6.2 µg/mL. Phytochemical investigation of this bioactive extract resulted in the isolation of fifteen compounds (<b>1</b>-<b>15</b>), including a new compound, subulatone A (-). The structure of compound <b>1</b> was elucidated using HRFABMS and NMR spectroscopic analyses. T  ...[more]

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