Review Article
Proteogenomics for Pediatric Brain Cancer
Margaret Simonian*
Corresponding Author: Margaret Simonian, UCLA, David Geffen School of Medicine, 611 Charles E. Young Drive, Los Angeles, CA 90095, USA.
Received: March 23, 2021; Revised: June 22, 2021; Accepted: June 25, 2021 Available Online: September 4, 2021
Citation: Simonian M. (2020) Proteogenomics for Pediatric Brain Cancer. Proteomics Bioinformatics, 2(3): 201-205.
Copyrights: ©2021 Simonian M. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Pediatric central nervous system tumors are the most common tumors in children, it constitutes 15% - 20% of all malignancies in children and are the leading cause of cancer related deaths in children. Proteogenomics is an emerging field of biological research that utilizes a combination of proteomics, genomics, and transcriptomics to aid in the discovery and identification of biomarkers for diagnosis and therapeutic purposes. Integrative proteogenomics analysis of pediatric tumors identified underlying biological processes and potential treatments as well as the functional effects of somatic mutations and copy number variation driving tumorigenesis.

Keywords: Proteogenomics, Brain cancer, Targeted therapy
 
INTRODUCTION

Pediatric brain tumors are the leading cause of cancer related deaths in children [1]. Pediatric brain tumors are masses of abnormal cells that occur in a child's brain, some are benign and some are malignant. Pediatric brain tumors treatment is different than adult brain tumors treatment and it depends on the type, size, and the location of the tumor within the brain, as well as the child's age and general health.

CURRENT TREATMENT OPTIONS

Surgery
Surgical removal is performed when the tumor is small in size and easily accessible for complete surgical removal. Although it carries risks especially when tumors can't be separated from surrounding tissue or when they are located near sensitive areas in the brain.

Radiation therapy (RT)

Such as X-rays or proton beam therapy that delivers high targeted doses of radiation to brain tumors, while minimizing radiation exposure to surrounding healthy tissues. RT has undergone comprehensive changes in recent decades to maximize the therapeutic benefit between efficacy and toxicity, such as the development of IMRT, VMAT and PBRT radiation therapy.

Radiosurgery

Stereotactic radiosurgery delivers multiple highly focused beam of radiation Gamma Knife or linear accelerator treatment to destroy the tumor in a small area. The point where all the beams meet receives the highest dose of radiation while minimizing the radiation exposure to surrounding tissues. Radiosurgery in children is important for treating unresectable tumors or recurrent tumors that have received prior radiotherapy.

Chemotherapy

Chemotherapy uses drugs to destroy cancer cells, normally injected through the vein (intravenous chemotherapy). The option of chemotherapy drugs depends on the type of cancer.

Targeted drug therapy

Targeted therapy uses drugs to target specific genes and proteins that are involved in the growth and survival of cancer cells, one example is bevacizumab that is used to treat low-grade gliomas [2] (Figure 1). Genomic techniques started to elucidate the pathogenesis of many pediatric brain tumors, however, there are some challenges that limit the translation of these findings into therapy [3-6]. The majority of pediatric brain tumors resist genomic targeted treatments. In addition, many pediatric brain tumors are characterized by deviant epigenetic landscapes, and there is no effective way to specifically target these changes [7].
Proteogenomics

Recently quantitative mass spectrometry analyses have advanced, adding a quantitative proteomics approach to a primarily genomics based biological understanding of cancers; this gave rise to a new emerging technology called “Proteogenomics” [8-10]. Proteogenomics utilizes a combination of proteomics, genomics, and transcriptomics to support the discovery and identification of peptides by comparing MS/MS spectra against a protein database from genomic and transcriptomic to improve gene annotations [10]. Therefore, analysis of integrated proteogenomics datasets has the potential to aid with identification of new therapeutic targets and avenues.

In 2020, Petralia [11] conducted a comprehensive proteogenomic study across major histological types of pediatric brain cancer. The analysis included whole-genome sequencing RNA sequencing (transcriptomics), proteomics (LC-MS, MRM, TMT) and phosphoproteomics characterization, of 218 tumors across 7 histological types of childhood brain cancer: low-grade glioma (LGG), high-grade glioma (HGG), ependymoma (EP), craniopharyngioma (CP) medulloblastoma (MB), ganglioglioma, and atypical teratoid rhabdoid tumor (ATRT). This was the first large-scale proteogenomics analysis across traditional histological boundaries to reveal foundational pediatric brain tumor biology and reveal rational treatment options [11] (Figure 2).
The Proteomics data identified familiar biological patterns across histological samples, suggesting that treatments used for one histological type may be applied effectively to other tumors with similar proteomics characteristics. The data further revealed functional effects of somatic mutations and copy number variations not visible in the transcriptomics data [11].

Kinase-substrate association and co-expression network analysis also identified important tumorigenesis mechanisms. Investigation of kinase activity based on phosphoproteomics showed that protein abundance can be reduced in active signaling pathways (e.g., ERK1/3 in CP), which could happen because of feedback loops in many complicated regulatory processes, suggesting the important role of phosphoproteomics data in characterizing pathway activities [11].

The proteomics/phosphoproteomics data clustering analyses uncovered two apparent subgroups of pediatric CP, with one subgroup showing similar proteomics/phosphoproteomics characteristics as pediatric LGG BRAFV600E tumors. This observation suggests potential use of MEK/MAPK inhibitors in a subset of pediatric CP, which currently has no effective chemotherapy options. The existence of these two subgroups of CP, was not evident from RNA data. Additionally, they observed a disagreement between RNA and protein abundance in other histologies, such as EP and LGG [11]. The low to moderate RNA-protein correlation in the study was consistent with other large-scale proteogenomics projects studies [8,12,13]. Multiple factors, such as protein turnover and selective translation, may have contributed to the low correlation between RNA and protein abundance. Interestingly, more aggressive tumors showed increased protein-RNA correlation, this occurrence was observed among multiple cancer proteogenomics studies [8,12]. One possible explanation is that aggressive tumors often have high proliferation, and the boosted translation activities in highly proliferative tumor cells result in more correlated RNA and protein signals. Hence, studying the proteome revealed insights that were not evident from RNA-based analysis alone [11].

Pediatric tumors normally have fewer genetic variation and somatic mutations compared to adult tumors [5,14,15]. However, few recurrent DNA alterations were observed in the above study. LGG tumors with BRAFV600E mutation had significantly downregulated BRAF protein abundance compared with BRAFWT LGG tumors where in fact the reduction was not significant at the transcript level. CTNNB1 mutation resulted in elevated protein/ RNA levels among CP samples, whereas NF1 mutation resulted in down regulation of associated proteins and transcripts in HGG. SMARCB1 RNA/protein were also significantly downregulated in ATRT samples and the downregulation was the result of different types of DNA alterations, including mutation, deletion, and copy-neutral loss of heterozygosity [11].

CONCLUSION

These studies demonstrated the ability of proteomics, phosphoproteomics, and kinase activity scores to elucidate active signaling processes within tumors types. Applying these capabilities in a clinical trial study could reveal valuable information regarding the biology of individual tumors that respond to a given therapy. Once signature proteomics targets are identified, MRM (multiple reaction monitoring) signatures can be developed to identify individuals in real time whose tumors display particular biologics hence, may respond to a treatment. Histologically similar tumors are usually treated differently in pediatric and adult patients, although they often differ in their genomic features, this study has shown that they do not always drive biology. Future work needs to utilize proteomics platforms to cross examine tumors whose incidence compass a large age range to answer questions regarding how biology changes across the spectrum and if treatments can be rearranged for maximum benefit. A future study gathering larger group of the less common brain tumor types would be instructive in identifying the biology that is unique to those tumors.
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