XPKM2 isoform-specific deletion reveals a differential requirement for pyruvate kinase in tumor cells Academic Article uri icon

Overview

MeSH Major

  • Breast Neoplasms
  • Gene Deletion
  • Mammary Neoplasms, Experimental
  • Pyruvate Kinase

abstract

  • The pyruvate kinase M2 isoform (PKM2) is expressed in cancer and plays a role in regulating anabolic metabolism. To determine whether PKM2 is required for tumor formation or growth, we generated mice with a conditional allele that abolishes PKM2 expression without disrupting PKM1 expression. PKM2 deletion accelerated mammary tumor formation in a Brca1-loss-driven model of breast cancer. PKM2 null tumors displayed heterogeneous PKM1 expression, with PKM1 found in nonproliferating tumor cells and no detectable pyruvate kinase expression in proliferating cells. This suggests that PKM2 is not necessary for tumor cell proliferation and implies that the inactive state of PKM2 is associated with the proliferating cell population within tumors, whereas nonproliferating tumor cells require active pyruvate kinase. Consistent with these findings, variable PKM2 expression and heterozygous PKM2 mutations are found in human tumors. These data suggest that regulation of PKM2 activity supports the different metabolic requirements of proliferating and nonproliferating tumor cells.

publication date

  • October 10, 2013

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC3850755

Digital Object Identifier (DOI)

  • 10.1016/j.cell.2013.09.025

PubMed ID

  • 24120138

Additional Document Info

start page

  • 397

end page

  • 409

volume

  • 155

number

  • 2