Results 61 to 70 of about 16,244 (260)
[11C]acetate PET Imaging is not Always Associated with Increased Lipogenesis in Hepatocellular Carcinoma in Mice [PDF]
PurposeAltered metabolism, including increased glycolysis and de novo lipogenesis, is one of the hallmarks of cancer. Radiolabeled nutrients, including glucose and acetate, are extensively used for the detection of various tumors, including ...
VanBrocklin, Henry F +9 more
core +1 more source
The RNA methyltransferase FTSJ3 drives lung squamous cell carcinoma progression by catalyzing 2′‐O‐methylation of HSPA5 mRNA, which stabilizes BOP1 through SUMOylation and activates DRP1/SREBP1‐mediated mitochondrial fission and fatty acid oxidation. Targeting this axis with liposomal siRNA potently suppresses tumor growth and metastasis ABSTRACT Lung ...
Qin Hu +4 more
wiley +1 more source
The production of the omega-3 long-chain polyunsaturated fatty acids (n-3 LCPUFA) eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) from alpha-linolenic acid (ALA) relies on the delta-6 desaturase (D6D) enzyme encoded by the Fads2 gene.
Blair MacLeod +9 more
doaj +1 more source
Growing evidence has shown the involvement of the gut–liver axis in lipogenesis and fat deposition. However, how the gut crosstalk with the liver and the potential role of gut–liver crosstalk in the lipogenesis of chicken remains largely unknown. In this
Can Chen +5 more
doaj +1 more source
Loss of regulation of lipogenesis in the Zucker diabetic (ZDF) rat
We present here a study on the role of leptin in the regulation of lipogenesis by examining the effect of dietary macronutrient composition on lipogenesis in the leptin receptor-defective Zucker diabetic fatty rat (ZDF) and its lean litter mate (ZL ...
Laszlo G. Boros +3 more
core +1 more source
Dietary fructose feeds hepatic lipogenesis via microbiota-derived acetate [PDF]
A genetic mouse model is used to reveal a two-pronged mechanism of fructose-induced de novo lipogenesis in the liver, in which fructose catabolism in hepatocytes provides a signal to promote lipogenesis, whereas fructose metabolism by the gut microbiota ...
Wellen, Kathryn E +33 more
core +1 more source
In normal hepatocytes, FBP1 forms compartmentalized complexes with PKM2, ENO1, and LDHA independent of its catalytic activity, inhibiting PKM2 activity and restricting excessive glycolysis. During MASLD progression, FBP1 downregulation markedly reduces the abundance of these complexes and releases the “hijacked” glycolytic enzymes, leading to PKM2 ...
Busong Wang +10 more
wiley +1 more source
Lack of adaptation in lipogenesis by hepatoma 9121
The “minimal deviation” hepatoma 9121, implanted in rats, was shown to biosynthesize fatty acids from acetate-l-14C at the same rate as normal rat liver but faster than host liver.
J.C. Elwood, Harold P. Morris
doaj +1 more source
Elucidation of the mechanism of lipogenesis and fat deposition is essential for controlling excessive fat deposition in chicken. Studies have shown that gut microbiota plays an important role in regulating host lipogenesis and lipid metabolism.
Tao Zhang +9 more
doaj +1 more source
Hypoxia attenuates and HBS promotes adipocyte lipogenesis.
A. Hypoxia inhibits adipocyte lipogenesis during differentiation: Lipogenesis measured by uptake of Adipo-Red reagent during visceral adipocyte differentiation in N, H conditions.
Garen Gaston (445971) +5 more
core +1 more source

