Journal Article

Lactate-mediated epigenetic reprogramming regulates formation of human pancreatic cancer-associated fibroblasts

Choudhary, Gaurav S, Patel, Brijesh, Gupta, Sonal, Aluri, Srinivas, Von Ahrens, Dagny, Yang, Lifeng, Zhao, Hongyun, Sohal, Davendra, Maitra, Anirban, Kwak, Changsoo, Verma, Amit, Bhagat, Prafulla, Suzuki, Masako, Batra, Surinder, Steidl, Ulrich, Giricz, Orsi, Bartenstein, Matthias, Bhattacharyya, Sanchari, Agarwal, Beamon, Bhagat, Tushar D, Achreja, Abhinav, Banerjee, Debabrata, Baddour, Joelle, Yu, Yiting, Zou, Yiyu, Goggins, Michael, Sahu, Srabani, Nagrath, Deepak, Pradhan, Kith, Dawlaty, Meelad, Greally, John, Gordon-Mitchell, Shanisha, Guerrero, Paola A

2019

Overview

Even though pancreatic ductal adenocarcinoma (PDAC) is associated with fibrotic stroma, the molecular pathways regulating the formation of cancer associated fibroblasts (CAFs) are not well elucidated. An epigenomic analysis of patient-derived and de-novo generated CAFs demonstrated widespread loss of cytosine methylation that was associated with overexpression of various inflammatory transcripts including CXCR4. Co-culture of neoplastic cells with CAFs led to increased invasiveness that was abrogated by inhibition of CXCR4. Metabolite tracing revealed that lactate produced by neoplastic cells leads to increased production of alpha-ketoglutarate (aKG) within mesenchymal stem cells (MSCs). In turn, aKG mediated activation of the demethylase TET enzyme led to decreased cytosine methylation and increased hydroxymethylation during de novo differentiation of MSCs to CAF. Co-injection of neoplastic cells with TET-deficient MSCs inhibited tumor growth in vivo. Thus, in PDAC, a tumor-mediated lactate flux is associated with widespread epigenomic reprogramming that is seen during CAF formation.

• Publisher: eLife Sciences Publications Ltd,eLife Sciences Publications, Ltd
• Subject: 5-Methylcytosine - analogs & derivatives / 5-Methylcytosine - metabolism / Adenocarcinoma / Animals / Cancer Biology / Cancer-Associated Fibroblasts - pathology / Carcinoma, Pancreatic Ductal - genetics / Carcinoma, Pancreatic Ductal - pathology / Cell culture / Cell cycle / Cell Line, Tumor / Cell Proliferation - drug effects / Cell Transformation, Neoplastic - drug effects / Cellular Reprogramming - drug effects / Cellular Reprogramming - genetics / CXCR4 protein / Cytosine / DNA methylation / DNA Methylation - drug effects / Epigenesis, Genetic - drug effects / Epigenetics / Fibroblasts / Gene expression / Genomes / Growth factors / Humans / Inflammation / Invasiveness / Ketoglutaric acid / Ketoglutaric Acids - metabolism / Lactic acid / Lactic Acid - pharmacology / Medical research / Mesenchymal Stem Cells - drug effects / Mesenchymal Stem Cells - metabolism / Mesenchyme / Metabolites / methylation / Mice / Neoplasm Invasiveness / pancreas / Pancreatic cancer / Pancreatic Neoplasms / Pancreatic Neoplasms - genetics / Pancreatic Neoplasms - pathology / Receptors, CXCR4 - metabolism / Stem cells / Stroma / Stromal Cells - drug effects / Stromal Cells - metabolism / Transcriptome - genetics