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In Silico Identification of Chiral Biflavonoids as Dual PI3Kα/mTOR Inhibitors
Francisca Fernanda Nunes Azevedo1, Francisca Joseli Freitas de Sousa1, Jonatas Martins Negreiro2
1Postgraduate Programme in Biochemistry, Department of Biochemistry at Federal University of Ceará, Fortaleza 60440-554, CE, Brazil.
Abstract:
The PI3K/AKT/mTOR pathway is crucial in regulating key processes in mammalian cells, and impairments of this pathway are associated with cell survival in several cancer types. PI3Kα is the second most mutated oncogenic protein, and its overactivation initiates a secondary signaling cascade that enhances, among others, the activity of mTOR complexes 1 and 2. Despite the importance of this pathway, there is a gap in identifying dual inhibitors targeting both PI3Kα and mTOR, which could potentially overcome the limitations of single-target therapies. In this study, advanced computational tools were employed to identify plant-derived compounds with selective or dual inhibitory potentials against PI3Kα and mTOR enzymes. Compounds were obtained from the NuBBe database, a catalogue of Brazilian natural compounds. Among the 1745 compounds docked against the PI3Kα and mTOR enzymes, four bioflavonoids (2-5) displaying atropisomerism stood out. These compounds were further investigated for their binding profile into the catalytic sites of PI3Kα and mTOR, considering the influence of their sense of chirality (Ra and Sa enantiomers). The results indicate that compound 2 had no enantiopreference for PI3Kα, while (Sa)-2 preferentially bound to mTOR. Compound 3 bound to mTOR in both configurations, while only (Ra)-3 bound to PI3Kα. Compound 4 showed no enantiomeric preference for either protein, whereas compounds (Ra)-5 bound to PI3Kα and (Sa)-5 bound to mTOR. Altogether, these findings highlight the potential of four novel bioflavonoid compounds exhibiting a sense of chirality as promising candidates for the rational design of new cancer therapeutics targeting PI3Kα and mTOR. These insights provide a robust foundation for developing potent dual inhibitors, offering new avenues for treating diseases associated with the hyperactivation of these enzymes. Furthermore, this research underscores the value of plant-derived natural products in developing effective therapeutic agents, contributing significantly to the field of medicinal plant research and advancing the frontier of medicinal chemistry.
Insights
Researchers identified four plant-derived bioflavonoids with chirality that show potential as dual inhibitors for the PI3Kα and mTOR pathways, offering new cancer therapeutic strategies.
Area of Science:
- Medicinal Chemistry
- Pharmacology
- Computational Biology
Background:
- The PI3K/AKT/mTOR pathway is vital for cell regulation and often dysregulated in cancer.
- PI3Kα mutations are common, leading to overactivation of downstream signaling, including mTOR.
- Current therapies targeting PI3Kα or mTOR individually have limitations; dual inhibitors are needed.
Purpose of the Study:
- To identify novel plant-derived compounds with dual inhibitory potential against PI3Kα and mTOR.
- To investigate the role of chirality in the binding affinity of these compounds to PI3Kα and mTOR.
Main Methods:
- Utilized advanced computational tools for molecular docking against PI3Kα and mTOR enzymes.
- Screened 1745 compounds from the NuBBe database of Brazilian natural products.
- Analyzed the binding profiles and enantiomeric preferences of selected bioflavonoids.
Main Results:
- Four chiral bioflavonoids (compounds 2-5) demonstrated selective or dual inhibitory potential.
- Specific enantiomers showed preferential binding to either PI3Kα or mTOR.
- (Sa)-2 preferentially bound to mTOR, (Ra)-3 to PI3Kα, and (Ra)-5 to PI3Kα while (Sa)-5 to mTOR.
Conclusions:
- Chiral bioflavonoids are promising candidates for developing dual PI3Kα/mTOR inhibitors.
- These findings support the rational design of novel cancer therapeutics.
- Highlights the therapeutic potential of Brazilian natural products in medicinal chemistry.
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