The role of phosphoinositide 3-kinase subunits in chronic thyroiditis
Background The risk of neoplastic transformation in patients with chronic thyroiditis (Hashimoto’s thyroiditis – HT) is slightly increased. Genetic background of this observation is still unclear. PI3K isoforms are linked with inflammatory and neoplastic processes, thus they appear to be interesting...
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Published in | Thyroid research Vol. 5; no. 1; p. 22 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
21.12.2012
BioMed Central Ltd BMC |
Subjects | |
Online Access | Get full text |
ISSN | 1756-6614 1756-6614 |
DOI | 10.1186/1756-6614-5-22 |
Cover
Summary: | Background
The risk of neoplastic transformation in patients with chronic thyroiditis (Hashimoto’s thyroiditis – HT) is slightly increased. Genetic background of this observation is still unclear. PI3K isoforms are linked with inflammatory and neoplastic processes, thus they appear to be interesting subjects of a research in this respect. The aim of our study was to assess the
PIK3CA
,
PIK3CB
,
PIK3CD
and
PIK3CG
genes expression levels in HT.
Methods
Following conventional cytological examination, 67 thyroid FNAB specimens, received from patients with HT, were quantitatively evaluated regarding
PIK3CA
,
PIK3CB
,
PIK3CD
and
PIK3CG
expression levels by real-time PCR in the ABI PRISM
®
7500 Sequence Detection System.
Results
The performed analysis has revealed significantly higher expression levels (RQ) of
PIK3CD
,
PIK3CG
and
PIK3CA
genes in comparison with
PIK3CB
gene (p<0.05) and significantly higher gene expression level of
PIK3CD
in comparison with
PIK3CA
(p<0.05).
Conclusion
The observed increased
PIK3CD
,
PIK3CG
genes expression in HT is probably related to lymphocyte infiltration commonly seen in this condition, however, the role of increased
PIK3CA
gene expression in the multi-step carcinogenesis process cannot be excluded. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1756-6614 1756-6614 |
DOI: | 10.1186/1756-6614-5-22 |