Molecular markers of aggressiveness of thyroid cancer

被引:21
作者
Ringel, Matthew D. [1 ,2 ,3 ]
机构
[1] Ohio State Univ, Coll Med, Div Endocrinol Diabet & Metab, Columbus, OH 43210 USA
[2] Ohio State Univ, Coll Med, Div Oncol, Columbus, OH 43210 USA
[3] Arthur G James Comprehens Canc Ctr, Columbus, OH USA
关键词
BRAF; methylation; microRNA; PI3; kinase; tyrosine kinase inhibitors; PROTEIN-KINASE PATHWAY; LYMPH-NODE METASTASIS; T1799A BRAF MUTATION; BRAF(V600E) MUTATION; PHOSPHATIDYLINOSITOL; 3-KINASE/AKT; RET/PTC REARRANGEMENTS; GENE-EXPRESSION; UNITED-STATES; PIK3CA GENE; PAPILLARY;
D O I
10.1097/MED.0b013e32832ff2cb
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review To review recent progress at defining molecular markers that predict the biological behavior of thyroid cancer. Recent findings Thyroid cancer behavior is defined by the effects of the initiating oncogene as well as secondary events in tumor cells and the tumor microenvironment that are both genetic and epigenetic. Over the past several years, there has been intense focus on identifying molecular markers to better predict the aggressiveness of thyroid cancers and also to define therapeutic targets. The results of recent articles in this area of work are summarized with a focus of differentiated follicular-cell-derived forms of thyroid cancer. Summary Clinical staging predicts tumor behavior in many cases, but does not allow true 'personalization' of initial therapy or identify potential therapeutic targets for patients with progressive disease that does not respond to standard therapies. Recent data point to several new opportunities to refine thyroid cancer treatment based on molecular information. Several highlighted articles have begun to apply this information with clinical intent.
引用
收藏
页码:361 / 366
页数:6
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