4.7 Article

Antitumor immunity and therapeutic properties of marine seaweeds-derived extracts in the treatment of cancer

Journal

CANCER CELL INTERNATIONAL
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12935-022-02683-y

Keywords

Seaweeds; Immunomodulation; Antitumor immunity; Apoptosis

Categories

Funding

  1. Science, Technology & Innovation Funding Authority (STDF)
  2. The Egyptian Knowledge Bank (EKB)

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This study evaluated the antitumor and antitumor immunological potentials of extracts from brown alga Padinapavonica and red alga Janiarubens. The extracts showed effective inhibition of liver cancer cells in vitro and enhanced antitumor immunity in vivo. They also reduced tumor cell viability and increased lymphocyte count while decreasing neutrophils and monocytes. These extracts have potential antitumor and immunological effects with low toxicity, suggesting further investigation into their mechanisms.
Marine seaweeds are important sources of drugs with several pharmacological characteristics. The present study aims to evaluate the antitumor and antitumor immunological potentials of the extracts from the brown alga Padinapavonica and the red alga Janiarubens, inhibiting the Egyptian marine coasts. Hep-G2 cell lines were used for assessment of the antitumor efficacy of Padinapavonica and Janiarubens extracts in vitro, while Ehrlich ascites carcinoma (EAC) cells were applied to gain more antitumor immunity and antitumor insights of P.pavonica and J.rubens extracts in vivo. In vitro antitumor potentials of P.pavonica and J.rubens extracts were analyzed against human liver cancer Hep-G2 cells by MTT and trypan blue exclusion assays. In vivo antitumor immunological potentials of P.pavonica and J.rubens extracts at low, high, and prophylactic doses were analyzed by blood counting and flow cytometry in mice challenged with Ehrlich ascites carcinoma (EAC) cells. In vitro results revealed that P.pavonica and J.rubens extracts caused significant decreases in the number and viability of Hep-G2 cells in a dose-dependent manner as compared to untreated Hep-G2 cells or Cisplatin (R)-treated Hep-G2 cells. In vivo findings showed that P.pavonica and J.rubens extracts at low, high, and prophylactic doses significantly reduced the number and viability of EAC tumor cells accompanied by increases in EAC apoptosis compared to naive EAC mouse. Additionally, P.pavonica and J.rubens extracts at low and prophylactic doses remarkably increased both the total WBC count and the relative numbers of lymphocytes and decreased the relative numbers of neutrophils and monocytes. Flow cytometric analysis showed that P.pavonica and J.rubens extracts at the treatment and the prophylactic doses resulted in a significant increase in the phenotypic expressions of CD4(+) T, CD8(+) T, and CD335 cells compared to naive EAC mouse. Overall, both extracts P.pavonica and J.rubens possess potential antitumor and antitumor immunological effects with less toxicity, opening new approaches for further studies of the chemical and biological mechanisms behind these effects.

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