Frontiers in Oncology (Jun 2022)

Cucurbitacin B, Purified and Characterized From the Rhizome of Corallocarpus epigaeus Exhibits Anti-Melanoma Potential

  • Sreekumar Usha Devi Aiswarya,
  • Sreekumar Usha Devi Aiswarya,
  • Gowda Vikas,
  • Nair Hariprasad Haritha,
  • Vijayasteltar Belsamma Liju,
  • Vijayasteltar Belsamma Liju,
  • Anwar Shabna,
  • Mundanattu Swetha,
  • Tennyson Prakash Rayginia,
  • Chenicheri Kizhakkeveettil Keerthana,
  • Lekshmi Raghu Nath,
  • Lekshmi Raghu Nath,
  • Mullan Vellandy Reshma,
  • Mullan Vellandy Reshma,
  • Sankar Sundaram,
  • Nikhil Ponnoor Anto,
  • Ravi Shankar Lankalapalli,
  • Ravi Shankar Lankalapalli,
  • Ruby John Anto,
  • Smitha Vadakkeveettil Bava

DOI
https://doi.org/10.3389/fonc.2022.903832
Journal volume & issue
Vol. 12

Abstract

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The ethnomedicinal plant from the Cucurbitaceae family, Corallocarpus epigaeus, or its bioactive derivatives have been widely utilized in traditional medicine owing to their distinct applications against various human ailments and have lured the interest of ethnobotanists and biochemists. Here, we report for the first time, the anti-cancer potential of a bio-active fraction isolated from the dried rhizome of C. epigaeus, and the bioactive principle identified as cucurbitacin B (Cu-B). The purification processes involving the utilization of multiple organic extracts of C. epigaeus rhizome powder, yielded Cu-B from the Ethyl acetate Cytotoxic Fraction (ECF), obtained by the chromatographic separation of the ethyl acetate extract. Amongst the various cancer lines tested, melanoma cells exhibit maximal sensitivity towards the Cu-B-containing ECF fraction. Cu-B induces an apoptotic mode of cell death initiated intrinsically as well as extrinsically in A375 melanoma cells whilst remaining comparatively less toxic to normal skin fibroblasts. In vivo studies involving a NOD-SCID murine model of human melanoma demonstrate the ability of Cu-B to attenuate tumor growth, while being pharmacologically safe in vivo, as assessed in Swiss albino mice. Furthermore, Cu-B inhibits MEK 1/2 as well as the constitutive and EGF-induced ERK 1/2 activation, indicating a definitive involvement of MAPK signal transducers in regulating Cu-B-mediated anti-melanoma activity. Together, our study demonstrates the anti-melanoma potential of C. epigaeus-derived Cu-B, which indicates the Cucurbitaceae succulent as a prospective source for deriving potent and pharmacologically safe anti-cancer compounds.

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