Positive Feedback Loop Between PI3K-Akt-mTORC1 Signaling and the Lipogenic Pathway Boosts Akt Signaling: Induction of the Lipogenic Pathway by a Melanoma Antigen

• Published in: Cancer research (Chicago, Ill.) Ill.), 2011-07, Vol.71 (14), p.4989-4997
• Main Authors: YAMAUCHI, Yoshio, FURUKAWA, Keiko, HAMAMURA, Kazunori, FURUKAWA, Koichi
• Format: Article
• Language: English
• Subjects: Animals; Antineoplastic agents; Biological and medical sciences; Dermatology; Feedback, Physiological; Female; Gangliosides - biosynthesis; Humans; Lipogenesis; Mechanistic Target of Rapamycin Complex 1; Medical sciences; Melanoma - immunology; Melanoma - metabolism; Membrane Microdomains - metabolism; Mice; Mice, Inbred BALB C; Multiprotein Complexes; Mutation; Oncogene Protein v-akt - metabolism; Pharmacology. Drug treatments; Phosphatidylinositol 3-Kinases - metabolism; Proteins - metabolism; Proto-Oncogene Proteins B-raf - genetics; Signal Transduction; Sterol Regulatory Element Binding Proteins - metabolism; TOR Serine-Threonine Kinases; Transplantation, Heterologous; Tumors; Tumors of the skin and soft tissue. Premalignant lesions
• ISSN: 0008-5472; 1538-7445
• DOI: 10.1158/0008-5472.can-10-4108

The lipogenic phenotype is a metabolic hallmark of cancer cells. Sterol regulatory element-binding proteins (SREBP) are key transcriptional factors to regulate biosynthesis of cholesterol and fatty acids. It has been poorly understood how the lipogenic phenotype in cancer cells is regulated and how it augments their malignant properties. Here we describe roles of the melanoma antigen ganglioside GD3 and phosphatidylinositol 3-kinase (PI3K)-Akt-mTOR complex 1 (mTORC1) signaling in the regulation of SREBP activity, cholesterol biosynthesis, and the integrity of lipid rafts in human melanoma cells. GD3 expression induced the activation of both SREBP-1 and SREBP-2. Consequently, HMG-CoA reductase expression and cholesterol biosynthesis increased. The activation of the SREBP pathway was independent of the oncogenic BRAF mutation. On the other hand, it was regulated by PI3K-Akt-mTORC1 signaling in human melanoma cells. Disruption of the signaling pathway resulted in the reduction of cholesterol in lipid rafts. Inhibition of the SREBP pathway attenuated Akt activation in lipid rafts and suppressed the growth of human melanoma cells in vitro and in vivo. These results suggest that PI3K-Akt-mTORC1 signaling is important for the integrity of lipid rafts by regulating SREBP activation and subsequent cholesterogenesis. We thus propose a positive feedback circuit in which PI3K-Akt-mTORC1-SREBP signaling boosts Akt signaling in human melanoma cells expressing GD3.