Journal Article

PRDM15 is a key regulator of metabolism critical to sustain B-cell lymphomagenesis

Andreacchio, Giuseppe, Uchenunu, Oro, Fong, Jia Yi, Di Tullio, Federico, Bernstein, Emily, Wee, Keng Boon, Varano, Gabriele, Ong, Chee Bing, Kaldis, Philipp, Mzoughi, Slim, Lim, Soon Thye, Jeyasekharan, Anand, Tan, Soo Yong, Pigini, Paolo, Huang, Dachuan, Wollmann, Heike, Dominguez-sola, David, Perini, Giovanni, Hoppe, Michal Marek, Low, Diana, Papadopoli, David, Wun, Cheng Mun, Koh, Cheryl M., Torre, Denis, Hasson, Dan, Teo, Shun Xie, Guccione, Ernesto, Motofeanu, Corina-Mihaela, Peng, Yanfen, Topisirovic, Ivan, Hulea, Laura, Ng, Siok-Bian, Ong, Choon Kiat, Hue, Susan Swee-Shan, Rajarethinam, Ravisankar, Al-Haddawi, Muthafar, Caldez, Matias J., Lakshmanan, Manikandan, Zhao, Julia N.

2020

Overview

PRDM (PRDI-BF1 and RIZ homology domain containing) family members are sequence-specific transcriptional regulators involved in cell identity and fate determination, often dysregulated in cancer. The PRDM15 gene is of particular interest, given its low expression in adult tissues and its overexpression in B-cell lymphomas. Despite its well characterized role in stem cell biology and during early development, the role of PRDM15 in cancer remains obscure. Herein, we demonstrate that while PRDM15 is largely dispensable for mouse adult somatic cell homeostasis in vivo, it plays a critical role in B-cell lymphomagenesis. Mechanistically, PRDM15 regulates a transcriptional program that sustains the activity of the PI3K/AKT/mTOR pathway and glycolysis in B-cell lymphomas. Abrogation of PRDM15 induces a metabolic crisis and selective death of lymphoma cells. Collectively, our data demonstrate that PRDM15 fuels the metabolic requirement of B-cell lymphomas and validate it as an attractive and previously unrecognized target in oncology. The transcriptional regulator PRDM15 is expressed at low levels in normal tissues but overexpressed in B-cell lymphomas. Here, the authors show that PRDM15 depletion does not affect adult somatic cell homeostasis but leads to a metabolic crisis which impairs B-cell lymphomagenesis.

• Publisher: Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
• Subject: 1-Phosphatidylinositol 3-kinase / 38 / 38/15 / 38/91 / 631/337/2019 / 631/67/1990/291/1621/1915 / 64/60 / 96/106 / 96/95 / AKT protein / Animals / Apoptosis - genetics / Apoptosis - physiology / B-cell lymphoma / Blotting, Western / Cancer / Cell death / Cell Survival - genetics / Cell Survival - physiology / Chromatin Immunoprecipitation / Computational Biology / Depletion / DNA-Binding Proteins - genetics / DNA-Binding Proteins - metabolism / Female / Flow Cytometry / Gene Expression Regulation - genetics / Gene Expression Regulation - physiology / Glycolysis / Homeostasis / Homology / Humanities and Social Sciences / Humans / Lymphocytes B / Lymphoma / Lymphoma - genetics / Lymphoma - metabolism / Metabolism / Mice / Mice, SCID / multidisciplinary / Oncology / Phosphatidylinositol 3-Kinases - genetics / Phosphatidylinositol 3-Kinases - metabolism / Random Allocation / Regulators / Science / Science (multidisciplinary) / Stem cells / TOR protein / Transcription / Transcription Factors - genetics / Transcription Factors - metabolism / Transcriptome - genetics