Clinicopathological significance of the CRTC3-MAML2 fusion transcript in mucoepidermoid carcinoma

被引:132
作者
Nakayama, Takahisa [2 ]
Miyabe, Satoru [2 ]
Okabe, Mitsukuni [3 ]
Sakuma, Hidenori [2 ]
Ijichi, Kei [4 ]
Hasegawa, Yasuhisa [5 ]
Nagatsuka, Hitoshi [6 ]
Shimozato, Kazuo [2 ]
Inagaki, Hiroshi [1 ]
机构
[1] Nagoya City Univ, Dept Pathol, Grad Sch Med Sci, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[2] Aichi Gakuin Univ, Sch Dent, Dept Maxillofacial Surg, Nagoya, Aichi 464, Japan
[3] Nagoya City Univ, Dept Oral & Maxillofacial Surg, Grad Sch Med Sci, Nagoya, Aichi 4678601, Japan
[4] Nagoya City Univ, Dept Neurootolaryngol, Grad Sch Med Sci, Nagoya, Aichi 4678601, Japan
[5] Aichi Canc Ctr Cent Hosp, Dept Head & Neck Surg, Nagoya, Aichi, Japan
[6] Okayama Univ, Dept Oral Pathol & Med, Grad Sch Med Dent & Pharmaceut Sci, Okayama, Japan
关键词
mucoepidermoid carcinoma; CRTC3-MAML2; fusion; clinicopathological study; prognosis; SYNOVIAL SARCOMA; WARTHINS TUMORS; GENE FUSION; MECT1-MAML2; SALIVARY; ACTIVATION; ONCOGENE; BEHAVIOR; GLANDS;
D O I
10.1038/modpathol.2009.126
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Mucoepidermoid carcinoma is the most common primary malignancy of the salivary gland. We and others showed that CRTC1-MAML2 gene fusion was associated with favorable clinicopathological tumor features. Recently, a novel gene fusion, CRTC3-MAML2, was reported as a rare gene alteration in a case of mucoepidermoid carcinoma. However, its frequency and clinicopathological significance remains unclear. In all, 101 cases of mucoepidermoid carcinoma and 89 cases of non-mucoepidermoid carcinoma of the salivary gland were analyzed, and RNA was extracted from formalin-fixed, paraffin-embedded specimens. In the CRTC family, there have been three genes, CRTC1, CRTC2, and CRTC3. We developed reverse transcription-polymerase chain reaction (RT-PCR) assays for CRTC1-MAML2, CRTC2-MAML2, and CRTC3-MAML2 fusions. Clinicopathological data of the patients were obtained from their clinical records. Of 101 cases of mucoepidermoid carcinoma, 34 (34%) and 6 (6%) were positive for CRTC1-MAML2 and CRTC3-MAML2 fusion transcripts. However, in the 89 cases of non-mucoepidermoid carcinoma, neither transcript was noted. In the former cases, CRTC1-MAML2 and CRTC3-MAML2 fusions were mutually exclusive. The other fusion, CRTC2-MAML2, was not detected. We confirmed that the clinicopathological features of CRTC1-MAML2-positive mucoepidermoid carcinomas indicated an indolent course. CRTC3-MAML2-positive mucoepidermoid carcinomas also had clinicopathologically favorable features; all cases showed a less advanced clinical stage, negative nodal metastasis, no high-grade tumor histology, and no recurrence or tumor-related death after surgical resection of the tumor. It is interesting to note that patients with CRTC3-MAML2-positive tumors (mean 36 years of age) were significantly younger that those with the CRTC1-MAML2 fusion (55 years) and those with fusion-negative tumors (58 years). In conclusion, CRTC3-MAML2 fusion, which is mutually exclusive with CRTC1-MAML2 fusion and specific to mucoepidermoid carcinoma, may be detected more frequently than previously expected. Mucoepidermoid carcinomas possessing CRTC3-MAML2 fusion may be associated with favorable clinicopathological features and patients may be younger than those with CRTC1-MAML2 fusion or those with no detectable gene fusion. Modern Pathology (2009) 22, 1575-1581; doi:10.1038/modpathol.2009.126; published online 11 September 2009
引用
收藏
页码:1575 / 1581
页数:7
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