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Large-scale transcriptomics-driven approach revealed overexpression of CRNDE as a poor survival prognosis biomarker in glioblastoma
ID
Sorokin, Maxim
(
Author
),
ID
Raevskiy, Mikhail
(
Author
),
ID
Zottel, Alja
(
Author
),
ID
Šamec, Neja
(
Author
),
ID
Skoblar Vidmar, Marija
(
Author
),
ID
Matjašič, Alenka
(
Author
),
ID
Zupan, Andrej
(
Author
),
ID
Mlakar, Jernej
(
Author
),
ID
Suntsova, Maria
(
Author
),
ID
Kuzmin, Denis V.
(
Author
),
ID
Buzdin, Anton A.
(
Author
),
ID
Jovchevska, Ivana
(
Author
)
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https://www.mdpi.com/2072-6694/13/14/3419
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Abstract
Glioblastoma is the most common and malignant brain malignancy worldwide, with a 10-year survival of only 0.7%. Aggressive multimodal treatment is not enough to increase life expectancy and provide good quality of life for glioblastoma patients. In addition, despite decades of research, there are no established biomarkers for early disease diagnosis and monitoring of patient response to treatment. High throughput sequencing technologies allow for the identification of unique molecules from large clinically annotated datasets. Thus, the aim of our study was to identify significant molecular changes between short- and long-term glioblastoma survivors by transcriptome RNA sequencing profiling, followed by differential pathway-activation-level analysis. We used data from the publicly available repositories The Cancer Genome Atlas (TCGA; number of annotated cases = 135) and Chinese Glioma Genome Atlas (CGGA; number of annotated cases = 218), and experimental clinically annotated glioblastoma tissue samples from the Institute of Pathology, Faculty of Medicine in Ljubljana corresponding to 2-58 months overall survival (n = 16). We found one differential gene for long noncoding RNA CRNDE whose overexpression showed correlation to poor patient OS. Moreover, we identified overlapping sets of congruently regulated differential genes involved in cell growth, division, and migration, structure and dynamics of extracellular matrix, DNA methylation, and regulation through noncoding RNAs. Gene ontology analysis can provide additional information about the function of protein- and nonprotein-coding genes of interest and the processes in which they are involved. In the future, this can shape the design of more targeted therapeutic approaches.
Language:
English
Keywords:
glioblastoma
,
noncoding RNA
,
long-term survival
,
CRNDE
,
RNA sequencing
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
MF - Faculty of Medicine
Publication status:
Published
Publication version:
Version of Record
Year:
2021
Number of pages:
18 str.
Numbering:
Vol. 13, iss. 14, art. 3419
PID:
20.500.12556/RUL-135720
UDC:
616-006
ISSN on article:
2072-6694
DOI:
10.3390/cancers13143419
COBISS.SI-ID:
69980163
Publication date in RUL:
29.03.2022
Views:
953
Downloads:
144
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Record is a part of a journal
Title:
Cancers
Shortened title:
Cancers
Publisher:
MDPI
ISSN:
2072-6694
COBISS.SI-ID:
517914137
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:
08.07.2021
Secondary language
Language:
Slovenian
Keywords:
glioblastom
,
nekodirajoča RNA
,
dolgoročno preživetje
Projects
Funder:
ARRS - Slovenian Research Agency
Project number:
Z3-1869
Name:
Razvoj anti-FREM2 nanotelesa in njegova uporaba pri ciljanju glioblastomskih celic
Funder:
ARRS - Slovenian Research Agency
Project number:
BI-RU 19/20-005
Funder:
Other - Other funder or multiple funders
Funding programme:
OmicsWay
Funder:
Other - Other funder or multiple funders
Funding programme:
Russian Federation, Ministry of Science and Higher Education
Project number:
075-15-2020-926
Name:
Digital biodesign and personalized healthcare
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