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. 2023 Jun 11;14(6):1250.
doi: 10.3390/genes14061250.

Papillary Thyroid Carcinoma: A thorough Bioinformatic Analysis of Gene Expression and Clinical Data

Affiliations

Papillary Thyroid Carcinoma: A thorough Bioinformatic Analysis of Gene Expression and Clinical Data

Iván Petrini et al. Genes (Basel). .

Abstract

The likelihood of being diagnosed with thyroid cancer has increased in recent years; it is the fastest-expanding cancer in the United States and it has tripled in the last three decades. In particular, Papillary Thyroid Carcinoma (PTC) is the most common type of cancer affecting the thyroid. It is a slow-growing cancer and, thus, it can usually be cured. However, given the worrying increase in the diagnosis of this type of cancer, the discovery of new genetic markers for accurate treatment and prognostic is crucial. In the present study, the aim is to identify putative genes that may be specifically relevant in PTC through bioinformatic analysis of several gene expression public datasets and clinical information. Two datasets from Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) dataset were studied. Statistics and machine learning methods were sequentially employed to retrieve a final small cluster of genes of interest: PTGFR, ZMAT3, GABRB2, and DPP6. Kaplan-Meier plots were employed to assess the expression levels regarding overall survival and relapse-free survival. Furthermore, a manual bibliographic search for each gene was carried out, and a Protein-Protein Interaction (PPI) network was built to verify existing associations among them, followed by a new enrichment analysis. The results revealed that all the genes are highly relevant in the context of thyroid cancer and, more particularly interesting, PTGFR and DPP6 have not yet been associated with the disease up to date, thus making them worthy of further investigation as to their relationship to PTC.

Keywords: GEO; RNA-seq gene expression data; TCGA; gene expression analysis; microarray gene expression data; statistical learning; thyroid cancer.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
DEGs found for each dataset: (a) Up-regulated in PTC; (b) Down-regulated in PTC.
Figure 2
Figure 2
Box plots assessing differential expression behavior of genes of interest (color green for normal samples and red for tumor samples).
Figure 3
Figure 3
Kaplan–Meier Overall Survival plots.
Figure 4
Figure 4
Kaplan–Meier Relapse-Free Survival plots.
Figure 5
Figure 5
PPI network for PTGFR, ZMAT3, GABRB2 and DPP6.

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