Molecular and radiological characterization of glioblastoma multiforme using magnetic resonance imaging.


Journal

Journal of neurosurgical sciences
ISSN: 1827-1855
Titre abrégé: J Neurosurg Sci
Pays: Italy
ID NLM: 0432557

Informations de publication

Date de publication:
Feb 2021
Historique:
pubmed: 13 7 2019
medline: 18 9 2021
entrez: 13 7 2019
Statut: ppublish

Résumé

Glioblastoma multiforme (GBM) is the most malignant, aggressive and common form of primary brain cancer. Currently, GBM is considered to be a homogenous mass as all its margins are treated equally at the time of resection. However, it is not known whether radiologically distinct regions of GBM are also distinct at molecular level. We conducted this study to see if radiologically distinct regions were also different at the molecular level. In 20 patients, MRI derived variance known as Apparent Diffusion Coefficient (ADC) was plotted against Contrast Enhancement (CE). Four radiologically distinct regions were identified: 1) high ADC and low CE; 2) low ADC and low CE; 3) high ADC and high CE; and 4) low ADC and high CE. Biopsy samples were collected from these four regions of interest in each patient and immunohistochemistry was conducted to characterize cellular features and identify oncogene and stem cell marker expressing cells. Markedly increased nuclear pleomorphism, cellularity and necrosis were seen in region 2. Oncogene IDH was expressed in all regions, however, it was highest in region 4. Stem cell marker, CD44 expression was highest in region 1 and lowest in region 2 and 3. The expression of CD133 was highest in region 3. This study shows that ADC/CE plot can divide GBM into four regions, whose heterogeneity is evidenced by differential expression of nuclear pleomorphism, necrosis, cellularity and mitotic rate as well as the expression of oncogene and stem cell markers.

Sections du résumé

BACKGROUND BACKGROUND
Glioblastoma multiforme (GBM) is the most malignant, aggressive and common form of primary brain cancer. Currently, GBM is considered to be a homogenous mass as all its margins are treated equally at the time of resection. However, it is not known whether radiologically distinct regions of GBM are also distinct at molecular level. We conducted this study to see if radiologically distinct regions were also different at the molecular level.
METHODS METHODS
In 20 patients, MRI derived variance known as Apparent Diffusion Coefficient (ADC) was plotted against Contrast Enhancement (CE). Four radiologically distinct regions were identified: 1) high ADC and low CE; 2) low ADC and low CE; 3) high ADC and high CE; and 4) low ADC and high CE. Biopsy samples were collected from these four regions of interest in each patient and immunohistochemistry was conducted to characterize cellular features and identify oncogene and stem cell marker expressing cells.
RESULTS RESULTS
Markedly increased nuclear pleomorphism, cellularity and necrosis were seen in region 2. Oncogene IDH was expressed in all regions, however, it was highest in region 4. Stem cell marker, CD44 expression was highest in region 1 and lowest in region 2 and 3. The expression of CD133 was highest in region 3.
CONCLUSIONS CONCLUSIONS
This study shows that ADC/CE plot can divide GBM into four regions, whose heterogeneity is evidenced by differential expression of nuclear pleomorphism, necrosis, cellularity and mitotic rate as well as the expression of oncogene and stem cell markers.

Identifiants

pubmed: 31298508
pii: S0390-5616.19.04760-X
doi: 10.23736/S0390-5616.19.04760-X
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

47-53

Auteurs

Fazal M Arain (FM)

Department of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan - fazal.arain@mail.edu.

Anjiya Shaikh (A)

Department of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.

Muhammad Waqas (M)

Department of Surgery, Aga Khan University, Karachi, Pakistan.

Muhammad U Tariq (MU)

Department of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.

Muhammad F Raghib (MF)

Department of Surgery, Aga Khan University, Karachi, Pakistan.

Ghulam Haider (G)

Department of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.

Muhammad S Shamim (MS)

Department of Surgery, Aga Khan University, Karachi, Pakistan.

Fatima Mubarak (F)

Department of Radiology, Aga Khan University, Karachi, Pakistan.

Sheema H Hassan (SH)

Department of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.

Syed A Enam (SA)

Department of Surgery, Aga Khan University, Karachi, Pakistan.

Adnan A Jabbar (AA)

Department of Oncology, Aga Khan University, Karachi, Pakistan.

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Classifications MeSH