Summary: Infiltrating gliomas are shaped by their genetic evolution and microenvironment, researchers report. The findings may help in the development of therapies to treat glioma brain tumors.
Source: University of Colorado
Researchers have discovered that infiltrating gliomas, a common brain and spinal cord tumor, are shaped by their genetic evolution and microenvironment, a finding that could lead to more targeted treatments.
“We have identified epigenetic alterations at a recurrence that are not only prognostic in some cases, but may lead to different treatment options for the various subtypes that can improve long-term survival,” said study co-author D. Ryan Ormond, MD, PhD, a University of Colorado Cancer Center member and associate professor of neurosurgery at the University of Colorado School of Medicine on the CU Anschutz Medical Campus.
The study was published May 31 in the journal Cell.
The researchers looked at how gliomas interact with the brain, change over time, develop treatment resistance and become more invasive.
They identified three distinct phenotypes or observable traits at glioma recurrence – neuronal, mesenchymal and proliferative. Each of them converge with cellular, genetic and histological features that reveal themselves at recurrence. Some of these are associated with less favorable outcomes.
In this study, scientists used participant samples from the Glioma Longitudinal Analysis Consortium or GLASS cohort, a consortium created to identify the drivers of treatment resistance in glioma.
They analyzed RNA and/or DNA sequencing data from pairs of tumors from 304 adult patients with isocitrate dehydrogenase (IDH) wild type and IDH-mutant gliomas.
The tumors recurred in specific ways depending on the IDH mutation status. The changes they underwent during recurrence depended on how they interacted with the microenvironments they inhabited.
Researchers found that many IDH-wild type tumors were more invasive at recurrence. Their neoplastic cells showed increased neuronal signaling programs, suggesting a possible role for neuronal interactions in sparking the tumor’s progression.
They also discovered that hypermutation, often induced by treatment with drugs like temozolomide, along with deletion of the CDKN2A gene, which makes tumor-suppressing proteins, was associated with a proliferation of tumor cells at recurrence in both glioma subtypes.
In both IDH-wild type and IDH-mutant tumors, the hypermutation was associated with increased numbers of stem-like neoplastic cells. The growth of these cells reduced overall patient survival rates.
“Collectively, these results indicate that genetic evolution at recurrence can alter neoplastic glioma cells toward a more proliferative phenotype that associates with poor prognosis,” the study said.
Ormond said that therapy resistance remains a serious obstacle for patients with glioma and to improve quality of life and survival it needs to be overcome. These findings, he said, will enable physicians to better target the cancer with new therapies and treatments.
About this brain cancer and genetics research news
Author: David Kelly
Source: University of Colorado
Contact: David Kelly – University of Colorado
Image: The image is in the public domain
Original Research: Closed access.
“Glioma progression is shaped by genetic evolution and microenvironment interactions” by Ryan Ormond et al. Cell
Glioma progression is shaped by genetic evolution and microenvironment interactions
- Longitudinal glioma evolution follows an IDH mutation-dependent trajectory
- Hypermutation and CDKN2A deletions underlie increased proliferation at recurrence
- Recurrent IDH-wild-type neoplastic cells up-regulate neuronal signaling programs
- Mesenchymal transitions associate with distinct myeloid cell interactions
The factors driving therapy resistance in diffuse glioma remain poorly understood. To identify treatment-associated cellular and genetic changes, we analyzed RNA and/or DNA sequencing data from the temporally separated tumor pairs of 304 adult patients with isocitrate dehydrogenase (IDH)-wild-type and IDH-mutant glioma.
Tumors recurred in distinct manners that were dependent on IDH mutation status and attributable to changes in histological feature composition, somatic alterations, and microenvironment interactions.
Hypermutation and acquired CDKN2A deletions were associated with an increase in proliferating neoplastic cells at recurrence in both glioma subtypes, reflecting active tumor growth.
IDH-wild-type tumors were more invasive at recurrence, and their neoplastic cells exhibited increased expression of neuronal signaling programs that reflected a possible role for neuronal interactions in promoting glioma progression.
Mesenchymal transition was associated with the presence of a myeloid cell state defined by specific ligand-receptor interactions with neoplastic cells.
Collectively, these recurrence-associated phenotypes represent potential targets to alter disease progression.