Combined Treatment of MCF-7 Cells with AICAR and Methotrexate, Arrests Cell Cycle and Reverses Warburg Metabolism through AMP-Activated Protein Kinase (AMPK) and FOXO1. Academic Article uri icon

Overview

abstract

  • Cancer cells are characterized by metabolic alterations, namely, depressed mitochondrial oxidation, enhanced glycolysis and pentose phosphate shunt flux to support rapid cell growth, which is called the Warburg effect. In our study we assessed the metabolic consequences of a joint treatment of MCF-7 breast cancer cells with AICAR, an inducer of AMP-activated kinase (AMPK) jointly with methotrexate (MTX), a folate-analog antimetabolite that blunts de novo nucleotide synthesis. MCF7 cells, a model of breast cancer cells, were resistant to the individual application of AICAR or MTX, however combined treatment of AICAR and MTX reduced cell proliferation. Prolonged joint application of AICAR and MTX induced AMPK and consequently enhanced mitochondrial oxidation and reduced the rate of glycolysis. These metabolic changes suggest an anti-Warburg rearrangement of metabolism that led to the block of the G1/S and the G2/M transition slowing down cell cycle. The slowdown of cell proliferation was abolished when mitotropic transcription factors, PGC-1α, PGC-1β or FOXO1 were silenced. In human breast cancers higher expression of AMPKα and FOXO1 extended survival. AICAR and MTX exerts similar additive antiproliferative effect on other breast cancer cell lines, such as SKBR and 4T1 cells, too. Our data not only underline the importance of Warburg metabolism in breast cancer cells but nominate the AICAR+MTX combination as a potential cytostatic regime blunting Warburg metabolism. Furthermore, we suggest the targeting of AMPK and FOXO1 to combat breast cancer.

publication date

  • February 26, 2016

Research

keywords

  • AMP-Activated Protein Kinases
  • Aminoimidazole Carboxamide
  • Antineoplastic Combined Chemotherapy Protocols
  • Breast Neoplasms
  • Cytostatic Agents
  • Energy Metabolism
  • Forkhead Transcription Factors
  • Methotrexate
  • Neoplasm Proteins
  • Ribonucleotides

Identity

PubMed Central ID

  • PMC4769015

Scopus Document Identifier

  • 84960395715

Digital Object Identifier (DOI)

  • 10.4161/cc.11.2.19006

PubMed ID

  • 26919657

Additional Document Info

volume

  • 11

issue

  • 2