| Literature DB >> 29547721 |
Ruiting Lin1, Siyuan Xia1, Changliang Shan2, Dong Chen1, Yijie Liu1, Xue Gao1, Mei Wang1, Hee-Bum Kang1, Yaozhu Pan3, Shuangping Liu4, Young Rock Chung5, Omar Abdel-Wahab5, Taha Merghoub5, Michael Rossi1, Ragini R Kudchadkar1, David H Lawson1, Fadlo R Khuri1, Sagar Lonial1, Jing Chen6.
Abstract
Dietary supplements such as vitamins and minerals are widely used in the hope of improving health but may have unidentified risks and side effects. In particular, a pathogenic link between dietary supplements and specific oncogenes remains unknown. Here we report that chondroitin-4-sulfate (CHSA), a natural glycosaminoglycan approved as a dietary supplement used for osteoarthritis, selectively promotes the tumor growth potential of BRAF V600E-expressing human melanoma cells in patient- and cell line-derived xenograft mice and confers resistance to BRAF inhibitors. Mechanistically, chondroitin sulfate glucuronyltransferase (CSGlcA-T) signals through its product CHSA to enhance casein kinase 2 (CK2)-PTEN binding and consequent phosphorylation and inhibition of PTEN, which requires CHSA chains and is essential to sustain AKT activation in BRAF V600E-expressing melanoma cells. However, this CHSA-dependent PTEN inhibition is dispensable in cancer cells expressing mutant NRAS or PI3KCA, which directly activate the PI3K-AKT pathway. These results suggest that dietary supplements may exhibit oncogene-dependent pro-tumor effects.Entities:
Keywords: BRAF-V600E; CSGlcA-T; chondroitin sulfate; diet; dietary supplement; melanoma
Mesh:
Substances:
Year: 2018 PMID: 29547721 PMCID: PMC5858191 DOI: 10.1016/j.molcel.2018.02.010
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970