Oncogenic PIK3CA Mutation and Dysregulation in Human Salivary Duct Carcinoma

被引:4
作者
Qiu, Wanglong [1 ,2 ]
Tong, Guo-Xia [1 ]
Turk, Andrew T. [1 ]
Close, Lanny G. [3 ]
Caruana, SalvatoreM. [3 ]
Su, Gloria H. [1 ,2 ,3 ]
机构
[1] Columbia Univ, Med Ctr, Dept Pathol, New York, NY 10032 USA
[2] Columbia Univ, Med Ctr, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
[3] Columbia Univ, Med Ctr, Dept Otolaryngol & Head & Neck Surg, New York, NY 10032 USA
关键词
PAPILLARY MUCINOUS NEOPLASM/CARCINOMA; HIGH-FREQUENCY; GLAND; GENE; CANCER; KRAS; BRAF; HEAD;
D O I
10.1155/2014/810487
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Salivary duct carcinoma (SDC) is an aggressive malignant tumor with a high mortality, which resembles high-grade breast ductal carcinoma in morphology. The parotid gland is the most common location. Its molecular genetic characteristics remain largely unknown. We have previously reported high incidence of PIK3CA somatic mutations in head and neck squamous cell carcinoma, particularly in pharyngeal cancers. Here we examined the PIK3CA gene expression status and hotspot mutations in six cases of SDC by immunohistochemistry and genomic DNA sequencing. Immunohistochemistry showed that PIK3CA expression was elevated in all six patients with SDC. By DNA sequencing, two hotspot mutations of the PIK3CA gene, E545K (exon 9) and H1047R (exon 20), were identified in two of the six cases. Our results support that oncogenic PIK3CA is upregulated and frequently mutated in human SDC, adding evidence that PIK3CA oncogenic pathway is critical in the tumorigenesis of SDC, and may be a plausible drug target for this rare disease.
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页数:7
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