Antiproliferative Activity of <i>Buddleja saligna</i> (Willd.) against Melanoma and <i>In Vivo</i> Modulation of Angiogenesis

Melanoma cells secrete pro-angiogenic factors, which stimulates growth, proliferation and metastasis, and therefore are key therapeutic targets. <i>Buddleja saligna</i> (BS), and an isolated triterpenoid mixture (DT-BS-01) showed a fifty percent inhibitory concentration (IC<sub>50&...

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Main Authors: Danielle Twilley (Author), Velaphi C. Thipe (Author), Navneet Kishore (Author), Pierce Bloebaum (Author), Catarina Roma-Rodrigues (Author), Pedro V. Baptista (Author), Alexandra R. Fernandes (Author), Mamoalosi A. Selepe (Author), Lenka Langhansova (Author), Kattesh Katti (Author), Namrita Lall (Author)
Format: Book
Published: MDPI AG, 2022-11-01T00:00:00Z.
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Summary:Melanoma cells secrete pro-angiogenic factors, which stimulates growth, proliferation and metastasis, and therefore are key therapeutic targets. <i>Buddleja saligna</i> (BS), and an isolated triterpenoid mixture (DT-BS-01) showed a fifty percent inhibitory concentration (IC<sub>50</sub>) of 33.80 ± 1.02 and 5.45 ± 0.19 µg/mL, respectively, against melanoma cells (UCT-MEL-1) with selectivity index (SI) values of 1.64 and 5.06 compared to keratinocytes (HaCat). Cyclooxygenase-2 (COX-2) inhibition was observed with IC<sub>50</sub> values of 35.06 ± 2.96 (BS) and 26.40 ± 4.19 µg/mL (DT-BS-01). BS (30 µg/mL) significantly inhibited interleukin (IL)-6 (83.26 ± 17.60%) and IL-8 (100 ± 0.2%) production, whereas DT-BS-01 (5 µg/mL) showed 51.07 ± 2.83 (IL-6) and 0 ± 6.7% (IL-8) inhibition. Significant vascular endothelial growth factor (VEGF) inhibition, by 15.84 ± 4.54 and 12.21 ± 3.48%, respectively, was observed. In the ex ovo chick embryo yolk sac membrane assay (YSM), BS (15 µg/egg) significantly reduced new blood vessel formation, with 53.34 ± 11.64% newly formed vessels. Silver and palladium BS nanoparticles displayed noteworthy SI values. This is the first report on the significant anti-angiogenic activity of BS and DT-BS-01 and should be considered for preclinical trials as there are currently no US Food and Drug Administration (FDA) approved drugs to inhibit angiogenesis in melanoma.
Item Description:10.3390/ph15121497
1424-8247