AI Article Synopsis

  • A growing number of studies on gene expression in thyroid tumors allows for validation across different data sets, but requires careful comparison methods.
  • The research aimed to assess how to compare data from different Affymetrix GeneChip generations and analyze gene expression to help create classifiers for benign thyroid nodules and verify a classifier for papillary thyroid carcinoma (PTC).
  • The findings highlight that using intraindividual samples improves the detection of changes in expression patterns, leading to the development of multigene classifiers for benign nodules and confirming the specificity of existing PTC classifiers.

Article Abstract

Context: There are an increasing number of studies analyzing gene expression profiles in various benign and malignant thyroid tumors. This creates the opportunity to validate results obtained from one microarray study with those from other data sets. This process requires rigorous methods for accurate comparison.

Objective: The ability to compare data sets derived from different Affymetrix GeneChip generations and the influence of intra- and interindividual comparisons of gene expression data were evaluated to build multigene classifiers of benign thyroid nodules to verify a previously proposed papillary thyroid carcinoma (PTC) classifier and to look for molecular pathways essential for PTC oncogenesis.

Methods: Gene expression profile data sets from autonomously functioning and cold thyroid nodules and from PTC were analyzed by support vector machines. GenMAPP analysis was used for PTC data analysis to examine the expression patterns of biologically relevant gene sets.

Results: Only intraindividual reference samples allowed the identification of subtle changes in the expression patterns of relevant signaling cascades, such as the MAPK pathway in PTC. Using an artificial intelligence approach, the autonomously functioning and cold thyroid nodule multigene classifiers were derived and evaluated by cross-comparisons.

Conclusion: We recommend defining classifiers within one generation of gene chips and subsequently checking them across different array generations. Using this approach, we have demonstrated the specificity of a previously reported PTC classifier on an independent collection of benign tumors. Moreover, we propose multigene classifiers for different types of benign thyroid nodules.

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Source
http://dx.doi.org/10.1210/jc.2005-1620DOI Listing

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