Glycogen drives tumour initiation and progression in lung adenocarcinoma

糖原驱动肺腺癌的肿瘤发生和发展

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作者:Harrison A Clarke # ,Tara R Hawkinson # ,Cameron J Shedlock ,Terrymar Medina ,Roberto A Ribas ,Lei Wu ,Zizhen Liu ,Xin Ma ,Yi Xia ,Yu Huang ,Xing He ,Josephine E Chang ,Lyndsay E A Young ,Jelena A Juras ,Michael D Buoncristiani ,Alexis N James ,Anna Rushin ,Matthew E Merritt ,Annette Mestas ,Jessica F Lamb ,Elena C Manauis ,Grant L Austin ,Li Chen ,Pankaj K Singh ,Jiang Bian ,Craig W Vander Kooi ,B Mark Evers ,Christine F Brainson ,Derek B Allison ,Matthew S Gentry ,Ramon C Sun

Abstract

Lung adenocarcinoma (LUAD) is an aggressive cancer defined by oncogenic drivers and metabolic reprogramming. Here we leverage next-generation spatial screens to identify glycogen as a critical and previously underexplored oncogenic metabolite. High-throughput spatial analysis of human LUAD samples revealed that glycogen accumulation correlates with increased tumour grade and poor survival. Furthermore, we assessed the effect of increasing glycogen levels on LUAD via dietary intervention or via a genetic model. Approaches that increased glycogen levels provided compelling evidence that elevated glycogen substantially accelerates tumour progression, driving the formation of higher-grade tumours, while the genetic ablation of glycogen synthase effectively suppressed tumour growth. To further establish the connection between glycogen and cellular metabolism, we developed a multiplexed spatial technique to simultaneously assess glycogen and cellular metabolites, uncovering a direct relationship between glycogen levels and elevated central carbon metabolites essential for tumour growth. Our findings support the conclusion that glycogen accumulation drives LUAD cancer progression and provide a framework for integrating spatial metabolomics with translational models to uncover metabolic drivers of cancer.

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