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pmid:24475040

A 16-gene signature distinguishes anaplastic astrocytoma from glioblastoma.

Soumya Alige Mahabala Rao · Sujaya Srinivasan · Irene Rosita Pia Patric · Alangar Sathyaranjandas Hegde · Bangalore Ashwathnarayanara Chandramouli · Arivazhagan Arimappamagan · Vani Santosh · Paturu Kondaiah · Manchanahalli R Sathyanarayana Rao · Kumaravel Somasundaram

PloS one · 2014 doi:10.1371/journal.pone.0085200

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
A 16-gene signature distinguishes anaplastic astrocytoma from glioblastoma.
doi
10.1371/journal.pone.0085200
pmid
24475040
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Soumya Alige Mahabala Rao
[1]
Sujaya Srinivasan
[2]
Irene Rosita Pia Patric
[3]
Alangar Sathyaranjandas Hegde
[4]
Bangalore Ashwathnarayanara Chandramouli
[5]
Arivazhagan Arimappamagan
[6]
Vani Santosh
[7]
Paturu Kondaiah
[8]
Manchanahalli R Sathyanarayana Rao
[9]
Kumaravel Somasundaram
journal
PloS one
year
2014
abstract
Anaplastic astrocytoma (AA; Grade III) and glioblastoma (GBM; Grade IV) are diffusely infiltrating tumors and are called malignant astrocytomas. The treatment regimen and prognosis are distinctly different between anaplastic astrocytoma and glioblastoma patients. Although histopathology based current grading system is well accepted and largely reproducible, intratumoral histologic variations often lead to difficulties in classification of malignant astrocytoma samples. In order to obtain a more robust molecular classifier, we analysed RT-qPCR expression data of 175 differentially regulated genes across astrocytoma using Prediction Analysis of Microarrays (PAM) and found the most discriminatory 16-gene expression signature for the classification of anaplastic astrocytoma and glioblastoma. The 16-gene signature obtained in the training set was validated in the test set with diagnostic accuracy of 89%. Additionally, validation of the 16-gene signature in multiple independent cohorts revealed that the signature predicted anaplastic astrocytoma and glioblastoma samples with accuracy rates of 99%, 88%, and 92% in TCGA, GSE1993 and GSE4422 datasets, respectively. The protein-protein interaction network and pathway analysis suggested that the 16-genes of the signature identified epithelial-mesenchymal transition (EMT) pathway as the most differentially regulated pathway in glioblastoma compared to anaplastic astrocytoma. In addition to identifying 16 gene classification signature, we also demonstrated that genes involved in epithelial-mesenchymal transition may play an important role in distinguishing glioblastoma from anaplastic astrocytoma.
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Class prediction analysis was performed by Prediction Analysis of Microarrays (PAM) using the PAM package in the R software (version 2.14.2). The method of the nearest shrunken centroids was used to identify a subgroup of genes that best characterizes a predefined class [20]. The prediction accuracy was estimated by 10-fold cross-validation.
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Class prediction analysis was performed by Prediction Analysis of Microarrays (PAM) using the PAM package in the R software (version 2.14.2). The method of the nearest shrunken centroids was used to identify a subgroup of genes that best characterizes a predefined class [20]. The prediction accuracy was estimated by 10-fold cross-validation.
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The paper used Prediction Analysis of Microarrays (PAM) with nearest shrunken centroids to derive a 16-gene classification signature from RT-qPCR expression data for 175 differentially regulated genes in anaplastic astrocytoma and glioblastoma samples.
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In order to obtain a more robust molecular classifier, we analysed RT-qPCR expression data of 175 differentially regulated genes across astrocytoma using Prediction Analysis of Microarrays (PAM) and found the most discriminatory 16-gene expression signature for the classification of anaplastic astrocytoma and glioblastoma.
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The paper used Prediction Analysis of Microarrays (PAM) with nearest shrunken centroids to derive a 16-gene classification signature from RT-qPCR expression data for 175 differentially regulated genes in anaplastic astrocytoma and glioblastoma samples.
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The diagnostic accuracy, sensitivity and specificity of 16-gene signature to discriminate AA and GBM in training set, test set and three independent cohorts (TCGA, GSE1993, GSE4422) of patient samples.
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Prediction Analysis of Microarrays (PAM) using nearest shrunken centroids and 10-fold cross-validation
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Class prediction analysis was performed by Prediction Analysis of Microarrays (PAM) using the PAM package in the R software (version 2.14.2). The method of the nearest shrunken centroids was used to identify a subgroup of genes that best characterizes a predefined class [20]. The prediction accuracy was estimated by 10-fold cross-validation.
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candidate
Automated Assays Laravel application and simulated adapters
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: kaplan_meier.
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For the TCGA dataset, the level 3 expression data from the Agilent platform was downloaded from the TCGA data portal (tcga-data.nci.nih.gov/).
basis
The paper names GSE1993, GSE4422, GSE4271 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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ore robust molecular classifier, we analysed RT-qPCR expression data of 175 differentially regula
[1]
robust molecular classifier, we analysed RT-qPCR expression data of 175 differentially regula
[2]
eoplastic control brain samples by real time RT-qPCR. For GBM cohort, we have used the expression
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lastic control brain samples by real time RT-qPCR. For GBM cohort, we have used the expression
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sections and was used for histopathology and immunohistochemistry (IHC). This study has been approved by the e
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for histopathology and immunohistochemistry (IHC). This study has been approved by the ethics
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originally derived from previously performed microarray study in our laboratory [16] (Table S2 in Fi
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enes was subjected to prediction analysis of microarray (PAM) in the training set. PAM analysis iden
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Complete file
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