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Updated: Jun 12, 2026

Processing of Primary Brain Tumor Tissue for Stem Cell Assays and Flow Sorting
Published on: September 25, 2012
Genetic and modifying factors that determine the risk of brain tumors
Terezinha de Cresci Braga Montelli1, Maria Terezinha Serrão Peraçoli, Silvia Regina Rogatto
1Botucatu Medical School, São Paulo State University, Rua General Telles 267, Botucatu, SP, Brazil. acmontelli@uol.com.br
Abstract:
Some modifying factors may determine the risk of brain tumors. Until now, it could not be attempted to identify people at risk and also to improve significantly disease progression. Current therapy consists of surgical resection, followed by radiation therapy and chemotherapy. Despite of these treatments, the prognosis for patients is poor. In this review, we highlight general aspects concerning genetic alterations in brain tumors, namely astrocytomas, glioblastomas, oligodendrogliomas, medulloblastomas and ependymomas. The influence of these genetic alterations in patients' prognosis is discussed. Mutagen sensitivity is associated with cancer risk. The convincing studies that linked DNA damages and DNA repair alterations with brain tumors are also described. Another important modifying factor is immunity. General immune response against cancer, tumor microenvironment and immune response, mechanisms of tumor escape, CNS tumor immunology, immune defects that impair anti-tumor systemic immunity in brain tumor patients and local immuno-suppressive factors within CNS are also reviewed. New hope to treatment perspectives, as dendritic-cell-based vaccines is summarized too. Concluding, it seems well established that there is association between brain tumor risk and mutagen sensitivity, which is highly heritable. Primary brain tumors cause depression in systemic host immunity; local immuno-suppressive factors and immunological characteristics of tumor cells may explain the poor prognosis and DNA damages responses can alert immune system. However, it is necessary to clarify if individuals with both constitutional defects in immune functions and genetic instability have higher risk of developing brain tumors. Cytogenetic prospective studies and gene copy number variations analysis also must be performed in peripheral lymphocytes from brain tumor patients.
Insights
Genetic instability and mutagen sensitivity increase brain tumor risk. Brain tumors also impact immunity, potentially explaining poor prognoses and suggesting new therapeutic avenues like vaccines.
Area of Science:
- Neuro-oncology
- Cancer Genetics
- Immunology
Background:
- Brain tumor prognosis remains poor despite current treatments like surgery, radiation, and chemotherapy.
- Identifying individuals at risk and improving disease progression for brain tumors is challenging.
Purpose of the Study:
- To review genetic alterations and their influence on prognosis in various brain tumors.
- To explore the role of mutagen sensitivity, DNA damage, and repair in brain tumor development.
- To examine the complex interplay between the immune system and brain tumors, including tumor microenvironment and escape mechanisms.
Main Methods:
- Literature review of genetic alterations in astrocytomas, glioblastomas, oligodendrogliomas, medulloblastomas, and ependymomas.
- Analysis of studies linking DNA damage and repair alterations to brain tumors.
- Review of research on CNS tumor immunology, immune response, and immunosuppressive factors.
Main Results:
- Mutagen sensitivity, a heritable factor, is associated with increased brain tumor risk.
- Primary brain tumors can suppress systemic immunity, and local immunosuppressive factors contribute to poor outcomes.
- DNA damage responses may alert the immune system, but further research is needed.
Conclusions:
- A strong association exists between brain tumor risk, heritable mutagen sensitivity, and genetic instability.
- Investigating individuals with combined immune defects and genetic instability may clarify higher risk.
- Further cytogenetic and gene copy number variation studies in peripheral lymphocytes are warranted.
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