Literature DB >> 33219891

Squalene deters drivers of RCC disease progression beyond VHL status.

Karthikeyan Rajamani1,2,3, Somasundaram S Thirugnanasambandan4, Chidambaram Natesan5, Sethupathy Subramaniam5, Balasubramanian Thangavel4, Natarajan Aravindan6.   

Abstract

Identifying drug candidates to target cellular events/signaling that evades von Hippel-Lindau tumor suppressor (VHL) gene interaction is critical for the cure of renal cell carcinoma (RCC). Recently, we characterized a triterpene-squalene derived from marine brown alga. Herein, we investigated the potential of squalene in targeting HIF-signaling and other drivers of RCC progression. Squalene inhibited cell proliferation, induced cell dealth and reverted the cells' metastatic state (migration, clonal expansion) independent of their VHL status. Near-identical inhibition of HIF-1α and HIF-2α and the regulation of downstream targets in VHL wild type and mutant cell lines demonstrated squalene efficacy beyond VHL-HIF interaction. In a rat model of chemically induced RCC, squalene displayed chemopreventive capabilities by substantial reversal of lipid peroxidation, mitochondrial redox regulation, maintaining ∆ψm, inflammation [Akt, nuclear factor κB (NF-κB)], angiogenesis (VEGFα), metastasis [matrix metalloproteinase 2 (MMP-2)], and survival (Bax/Bcl2, cytochrome-c, Casp3). Squalene restored glutathione, glutathione reductase, glutathione-s-transferase, catalase, and superoxide dismutase and stabilized alkaline phosphatase, alkaline transaminase, and aspartate transaminase. The correlation of thiobarbituric acid reactive substance with VEGF/NF-κB and negative association of GSH with Casp3 show that squalene employs reduction in ROS regulation. Cytokinesis-block micronuclei (CBMN) assay in VHLwt/mut cells revealed both direct and bystander effects of squalene with increased micronucleus (MN) frequency. Clastogenicity analysis of rat bone marrow cells demonstrated an anti-clastogenic effect of squalene, with increased polychromatic erythrocytes (PCEs), decreased MNPCE,s and MN normochromatic erythrocytes. Squalene could effectively target HIF signaling that orchestrate RCC evolution. The efficacy of squalene is similar in VHLwt and VHLmut RCC cells, and hence, squalene could serve as a promising drug candidate for an RCC cure beyond VHL status and VHL-HIF interaction dependency. Summary: Squalene derived from marine brown algae displays strong anti-cancer (RCC) activity, functionally targeting HIF-signaling pathway, and affects various cellular process. The significance of squalene effect for RCC is highlighted by its efficiency beyond VHL status, designating itself a promising drug candidate. Graphical abstract.
© 2020. Springer Nature B.V.

Entities:  

Keywords:  Chemoprevention; HIF signaling; Renal cell carcinoma; Squalene; Tumor progression; VHL

Mesh:

Substances:

Year:  2020        PMID: 33219891     DOI: 10.1007/s10565-020-09566-w

Source DB:  PubMed          Journal:  Cell Biol Toxicol        ISSN: 0742-2091            Impact factor:   6.691


  67 in total

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Journal:  Cell Stem Cell       Date:  2009-03-06       Impact factor: 24.633

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Review 6.  Epidemiology of Renal Cell Carcinoma.

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8.  Biophysical characterization of asolectin-squalene liposomes.

Authors:  Maria Assunta Costa; Maria Rosalia Mangione; Radha Santonocito; Rosa Passantino; Daniela Giacomazza; Fabio Librizzi; Oscar Moran; Rita Carrotta
Journal:  Colloids Surf B Biointerfaces       Date:  2018-06-19       Impact factor: 5.268

9.  Polyphenols from marine brown algae target radiotherapy-coordinated EMT and stemness-maintenance in residual pancreatic cancer.

Authors:  Sheeja Aravindan; Satish Kumar Ramraj; Somasundaram T Somasundaram; Terence S Herman; Natarajan Aravindan
Journal:  Stem Cell Res Ther       Date:  2015-09-22       Impact factor: 6.832

10.  Anti-pancreatic cancer deliverables from sea: first-hand evidence on the efficacy, molecular targets and mode of action for multifarious polyphenols from five different brown-algae.

Authors:  Sheeja Aravindan; Caroline R Delma; Somasundaram S Thirugnanasambandan; Terence S Herman; Natarajan Aravindan
Journal:  PLoS One       Date:  2013-04-16       Impact factor: 3.240

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3.  Cholesterol Auxotrophy as a Targetable Vulnerability in Clear Cell Renal Cell Carcinoma.

Authors:  Nicolas Skuli; M Celeste Simon; Romain Riscal; Caroline J Bull; Clementina Mesaros; Jennifer M Finan; Madeleine Carens; Elaine S Ho; Jimmy P Xu; Jason Godfrey; Paul Brennan; Mattias Johansson; Mark P Purdue; Stephen J Chanock; Daniela Mariosa; Nicholas J Timpson; Emma E Vincent; Brian Keith; Ian A Blair
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