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Biosynthesis of a Flavonol from a Flavanone by Establishing a One-pot Bienzymatic Cascade
Published on: August 14, 2019
HLBT-100: a highly potent anti-cancer flavanone from Tillandsia recurvata (L.) L
Henry I C Lowe1,2,3, Ngeh J Toyang2,3, Charah T Watson1
1Bio-Tech R&D Institute, University of the West Indies, 6 St. Johns Close, Mona, Jamaica.
Background:
The incidence and mortalities from cancers remain on the rise worldwide. Despite significant efforts to discover and develop novel anticancer agents, many cancers remain in the unmet need category. As such, efforts to discover and develop new and more effective and less toxic agents against cancer remain a top global priority. Our drug discovery approach is natural products based with a focus on plants. Tillandsia recurvata (L.) L. is one of the plants selected by our research team for further studies based on previous bioactivity findings on the anticancer activity of this plant.
Methods:
The plant biomass was extracted using supercritical fluid extraction technology with CO2 as the mobile phase. Bioactivity guided isolation was achieved by use of chromatographic technics combined with anti-proliferative assays to determine the active fraction and subsequently the pure compound. Following in house screening, the identified molecule was submitted to the US National Cancer Institute for screening on the NCI60 cell line panel using standard protocols. Effect of HLBT-100 on apoptosis, caspase 3/7, cell cycle and DNA fragmentation were assessed using standard protocols. Antiangiogenic activity was carried out using the ex vivo rat aortic ring assay.
Results:
A flavonoid of the flavanone class was isolated from T. recurvata (L.) L. with potent anticancer activity. The molecule was code named as HLBT-100 (also referred to as HLBT-001). The compound inhibited brain cancer (U87 MG), breast cancer (MDA-MB231), leukemia (MV4-11), melanoma (A375), and neuroblastoma (IMR-32) with IC50 concentrations of 0.054, 0.030, 0.024, 0.003 and 0.05 µM, respectively. The molecule also exhibited broad anticancer activity in the NCI60 panel inhibiting especially hematological, colon, CNS, melanoma, ovarian, breast and prostate cancers. Twenty-three of the NCI60 cell lines were inhibited with GI50 values <0.100 µM. In terms of potential mechanisms of action, the molecule demonstrated effect on the cell cycle as evidenced by the accumulation of cells with
Conclusion:
This paper describes for the first time the anticancer activity of HLBT-100 isolated from T. recurvate (L.) L. The broad and selective anticancer activity of HLBT-100 as evidenced by its potent activity against IMR-32, CNS cancer cell line while not active against neuro-2a, a normal CNS cell line. The activity demonstrated by HLBT-100 in these studies makes the molecule a potential candidate for further development targeting especially those cancers that remain in the unmet need category such as glioblastoma multiforme and acute myeloid leukemia in addition to other cancers.
Insights
A novel flavonoid, HLBT-100, isolated from Tillandsia recurvata, shows potent anticancer activity against various cancer cell lines. This natural compound induces apoptosis and inhibits angiogenesis, presenting a promising candidate for new cancer therapies.
Area of Science:
- Natural Product Chemistry
- Pharmacology
- Oncology
Background:
- Global cancer incidence and mortality rates continue to rise, highlighting the urgent need for novel, effective, and less toxic anticancer agents.
- Natural products, particularly from plants, represent a rich source for drug discovery, with Tillandsia recurvata identified as a promising candidate due to prior bioactivity findings.
Purpose of the Study:
- To isolate and characterize a novel anticancer compound from Tillandsia recurvata (L.) L.
- To evaluate the anticancer efficacy and mechanism of action of the isolated compound, designated HLBT-100.
Main Methods:
- Supercritical fluid extraction with CO2 was employed to extract compounds from Tillandsia recurvata biomass.
- Bioactivity-guided isolation using chromatography and anti-proliferative assays led to the identification of HLBT-100.
- HLBT-100 was screened against the NCI-60 cell line panel and its effects on apoptosis, caspase 3/7 activation, cell cycle, DNA fragmentation, and angiogenesis were assessed.
Main Results:
- A flavanone flavonoid, HLBT-100, was isolated from Tillandsia recurvata and demonstrated potent anticancer activity across multiple cancer types, including brain, breast, leukemia, melanoma, and neuroblastoma.
- HLBT-100 exhibited broad anticancer activity in the NCI-60 panel, with significant inhibition (GI50 < 0.100 µM) observed in hematological, colon, CNS, melanoma, ovarian, breast, and prostate cancers.
- The compound induced cell cycle arrest at
Conclusions:
- This study reports the anticancer activity of HLBT-100, a novel compound isolated from Tillandsia recurvata.
- HLBT-100 displays broad and selective anticancer properties, showing potent activity against cancer cell lines like IMR-32 (CNS cancer) while sparing normal CNS cells (neuro-2a).
- HLBT-100 is a promising candidate for further development, particularly for cancers with unmet treatment needs such as glioblastoma multiforme and acute myeloid leukemia.
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