Metabolic Protein Wields Phosphate Group to Activate Cancer-Promoting Genes
Source Newsroom: University of Texas M. D. Anderson Cancer Center
UT MD Anderson scientists show how PKM2 contributes to brain tumor formation and growth
Newswise — HOUSTON - A metabolic protein that nourishes cancer cells also activates tumor-promoting genes by loosening part of the packaging that entwines DNA to make up chromosomes, a team led by scientists at The University of Texas MD Anderson Cancer Center reports in the Aug. 16 issue of Cell.
Working in cell lines and mouse models of glioblastoma multiforme, the most lethal form of brain tumor, senior author Zhimin Lu, Ph.D., associate professor of Neuro-Oncology at MD Anderson, and colleagues show that pyruvate kinase M2 (PKM2) fuels tumor growth by influencing a histone protein.
DNA is packaged in and spooled around histone proteins. The researchers found that PKM2 tags histone H3 with a phosphate group (one atom of phosphorous, four of oxygen) in a specific location called T11.
'No phosphorylation of H3, no tumor'
This phosphorylation leads to activation of the tumor-promoting genes, increased tumor cell reproduction and formation of tumors, Lu said. "If there's no phosphorylation of H3, there's no tumor. It's that crucial to glioblastoma formation."
An analysis of 85 human glioblastomas indicated that higher levels of PKM2 expression in the cell nucleus and of H3 phosphorylation are correlated with shorter survival. A separate analysis showed higher levels of H3 phosphorylation associated with higher grade tumors in a comparison of 30 low-grade tumor samples and 45 high grade glioblastomas.
"Histone 3-T11 phosphorylation has great potential to serve as both a prognostic marker and a guide for the use of PKM2-inhibiting therapies once they are developed," Lu said.
PKM2 has long been known for its well-established role in aerobic glycolysis - the processing of glucose into energy that solid tumors, glioblastomas in particular, rely on heavily to survive and grow. Lu and colleagues have been teasing out the mechanisms of PKM2's other role - the transcription and activation of genes.
It all starts with EGFR
When the epidermal growth factor receptor (EGFR) on the cell's membrane is activated by a growth factor, the PKM2 protein moves into the cell nucleus, where it binds to the promoter regions of genes. Other proteins called transcription factors attach to a gene's promoter region to activate it.
Cancer cells have high levels of EGFR on the cell surface, relaying growth signals from outside the cell inside. EGFR is itself a target of some cancer drugs.
A series of experiments by the research team uncovered the following molecular steps:
* After EGFR activation, PKM2 binds to histone H3 and attaches a phosphate group at T11.
* This separates another protein called histone deacetylase 3 (HDAC3) from the promoter regions of the genes CCND1 and MYC. HDACs block gene activation.
* With the HDACs gone, histone H3 acquires an acetyl group, which facilitates gene activation.
"This series of events only occurs when H3 is phosphorylated by PKM2," Lu said.
Blocking phosphorylation prevents brain tumors in mice
CCND1 expresses the protein cyclin D1, a cell cycle regulator. The MYC gene is frequently mutated in cancer, leading to overexpression of the transcription factor Myc, which in turn causes unregulated expression of many other genes.
Mouse experiments of EGFR-driven glioblastoma using reconstituted H3 histones, one normal and one with a mutant version of H3-T11A to prevent phosphorylation by PKM2, confirmed the relationship. Mice injected with normal, or wild type, H3, had an average tumor volume of nearly 40 cubic millimeters, while those with disabled T11A, blocking the phosphorylation point for PKM2, had no tumors.
"Our findings establish PKM2 as a histone kinase, which directly regulates gene transcription and controls cell cycle progression and proliferation of tumor cells" Lu said. Kinases are a class of proteins that attach phosphate groups to other proteins.
Co-authors with Lu are first author Weiwei Yang, Ph.D., Yan Xia, Ph.D., Xinjian Li, Ji Liang, Ph.D, and W.K. Alfred Yung, M.D., all of MD Anderson's Department of Neuro-Oncology; David Hawke, Ph.D., of MD Anderson's Department of Molecular Pathology, Kenneth Aldape, M.D., of MD Anderson's Department of Pathology; Dongming Xing of School of Life Sciences, Tsinghua University in Beijing; and Tony Hunter, Ph.D., of the Salk Institute for Biological Studies in La Jolla, Calif.
Project funding was provided by grants from the National Cancer Institute of the National Institutes of Health (CA109035, CA127001-03, CA082683) including MD Anderson's Cancer Center Support Grant (CA16672) and also by grants from the Cancer Prevention and Research Institute of Texas, the American Cancer Society and the Sister Institution Network Fund at MD Anderson.