Branched-chain amino acids sustain pancreatic cancer growth by regulating lipid metabolism

Abstract

Branched-chain amino acid (BCAA) catabolism and high levels of enzymes in the BCAA metabolic pathway have recently been shown to be associated with cancer growth and survival. However, the precise roles of BCAA metabolism in cancer growth and survival remain largely unclear. Here, we found that BCAA metabolism has an important role in human pancreatic ductal adenocarcinoma (PDAC) growth by regulating lipogenesis. Compared with nontransformed human pancreatic ductal (HPDE) cells, PDAC cells exhibited significantly elevated BCAA uptake through solute carrier transporters, which were highly upregulated in pancreatic tumor tissues compared with normal tissues. Branched-chain amino-acid transaminase 2 (BCAT2) knockdown markedly impaired PDAC cell proliferation, but not HPDE cell proliferation, without significant alterations in glutamate or reactive oxygen species levels. Furthermore, PDAC cell proliferation, but not HPDE cell proliferation, was substantially inhibited upon knockdown of branched-chain α-keto acid dehydrogenase a (BCKDHA). Interestingly, BCKDHA knockdown had no significant effect on mitochondrial metabolism; that is, neither the level of tricarboxylic acid cycle intermediates nor the oxygen consumption rate was affected. However, BCKDHA knockdown significantly inhibited fatty-acid synthesis, indicating that PDAC cells may utilize BCAAs as a carbon source for fatty-acid biosynthesis. Overall, our findings show that the BCAA metabolic pathway may provide a novel therapeutic target for pancreatic cancer.

Pancreatic cancer: targeting a link between amino acids and lipids

Essential nutrient molecules called branched-chain amino acids (BCAAs) sustain pancreatic cancer by supporting the formation of fatty ‘lipid’ compounds, offering possible new approaches for treatment. Jaekyoung Son and colleagues at the University of Ulsan College of Medicine in Seoul, South Korea, explored the role of BCAAs in the most common form of pancreatic cancer, pancreatic ductal adenocarcinoma. Effective treatments are urgently required as the disease is generally diagnosed too late for surgery, the most effective treatment, to be successful. The researchers found that human cancer cells exploit increased uptake of BCAAs as a source of carbon to build lipids. Disabling the genes for enzymes that convert BCAAs into lipids significantly and selectively reduced cancer cell growth. Drugs that interfere with key points in the over-active uptake of BCAA and conversion to lipids could be developed into new therapies.