Head and neck adenoid cystic carcinoma: what is new in biological markers and treatment?

被引:22
作者
Bell, Diana [1 ]
Hanna, Ehab Y. [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Head & Neck Surg, Houston, TX 77030 USA
关键词
adenoid cystic carcinoma; biomarkers; cancer stem-like cells; molecular; HIGH-GRADE TRANSFORMATION; SALIVARY-GLAND NEOPLASMS; COPY NUMBER ALTERATIONS; C-KIT; TUMOR-SUPPRESSOR; MYB EXPRESSION; GENE FUSION; PHASE-II; HETEROZYGOSITY; CANCER;
D O I
10.1097/MOO.0b013e32835c05fd
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Purpose of review The purpose of this article is to provide a current review of publications on the molecular and basic science research findings for adenoid cystic carcinoma. Recent findings Findings related to adenoid cystic carcinoma carcinogenesis are discussed, including those involving cytogenetics, oncogenes, epigenetic alterations, biomarker studies, xenografts, and cancer stem-like cells. The defining molecular feature of adenoid cystic carcinoma is the presence of a recurrent chromosomal translocation, t(6; 9) (q22-23; p23-24), with the fusion transcript involving the genes MYB and NFIB. Molecular markers have been investigated and different targeted therapies have been explored, but unfortunately, none of these efforts has, to date, significantly improved outcomes in these patients. Summary The identification of molecular abnormalities underlying adenoid cystic carcinoma and those responsible for carcinogenesis is paramount to the development of specific targeted therapies. The design of robust clinical trials with embedded translational research is critical in determining the dosing, schedules, and combinations of such therapies. Further progress in this challenging field will require multicenter cooperation to compile molecular databases and to initiate prospective trials to determine the roles of promising new agents.
引用
收藏
页码:124 / 129
页数:6
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