Shinmura Kazuya, Kato Hisami, Igarashi Hisaki, Inoue Yusuke, Nakamura Satoki, Du Chunping, Kurachi Kiyotaka, Nakamura Toshio, Ogawa Hiroshi, Tanahashi Masayuki, Niwa Hiroshi, Sugimura Haruhiko
Department of Tumor Pathology, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi Ward, Hamamatsu, Shizuoka, 431-3192, Japan,
Pathol Oncol Res. 2015 Jul;21(3):759-64. doi: 10.1007/s12253-014-9887-2. Epub 2015 Jan 10.
A CD44-SLC1A2 fusion has recently been discovered in a subset of primary gastric cancers, and an APIP-SLC1A2 fusion has been described in a colon cancer cell line (SNU-C1); however, whether such SLC1A2 fusions occur in primary colorectal cancer (CRC) and whether such fusions are specific for gastrointestinal cancers remain uncertain. In the present study, we examined 90 primary CRCs and 112 primary non-small cell lung cancers (NSCLCs) for CD44-SLC1A2 and APIP-SLC1A2 fusion transcripts using RT-PCR and subsequent sequencing analyses. Although the expression of both types of SLC1A2 fusion transcripts was not detected in any of the NSCLCs, the expression of CD44-SLC1A2, but not the APIP-SLC1A2 fusion transcript, was detected in one (1.1 %) CRC. The CD44-SLC1A2 fusion transcript was expressed in cancerous tissue but not in corresponding non-cancerous tissue, and the fusion occurred between exon 1 of CD44 and exon 2 of SLC1A2; it was expected that a slightly truncated but functional SLC1A2 protein would be produced under the CD44 promoter. A quantitative RT-PCR analysis revealed that SLC1A2 mRNA expression was upregulated in CRC containing SLC1A2 fusion transcripts, while it was downregulated in most other CRCs. The SLC1A2 fusion-positive carcinoma was located on the right-side of colon, was a mucinous adenocarcinoma, was immunohistochemically negative for MSH2 mismatch repair protein, and contained no APC or KRAS mutations. Together, these results suggest that the expression of SLC1A2 fusion transcripts is related to a subset of primary CRCs and may contribute to the elucidation of the characteristics of SLC1A2 fusion-positive CRCs in the future.
最近在一部分原发性胃癌中发现了CD44-SLC1A2融合基因,并且在一种结肠癌细胞系(SNU-C1)中描述了APIP-SLC1A2融合基因;然而,此类SLC1A2融合基因是否存在于原发性结直肠癌(CRC)中以及此类融合基因是否为胃肠道癌所特有仍不确定。在本研究中,我们使用逆转录聚合酶链反应(RT-PCR)及后续测序分析,检测了90例原发性CRC和112例原发性非小细胞肺癌(NSCLC)中的CD44-SLC1A2和APIP-SLC1A2融合转录本。虽然在所有NSCLC中均未检测到两种类型的SLC1A2融合转录本的表达,但在1例(1.1%)CRC中检测到了CD44-SLC1A2融合转录本的表达,而未检测到APIP-SLC1A2融合转录本的表达。CD44-SLC1A2融合转录本在癌组织中表达,而在相应的非癌组织中未表达,且该融合发生在CD44的外显子1与SLC1A2的外显子2之间;预计在CD44启动子的作用下会产生一种略有截短但有功能的SLC1A2蛋白。定量RT-PCR分析显示,含有SLC1A2融合转录本的CRC中SLC1A2 mRNA表达上调,而在大多数其他CRC中则下调。SLC1A2融合阳性癌位于结肠右侧,为黏液腺癌,错配修复蛋白MSH2免疫组化阴性,且无APC或KRAS突变。总之,这些结果表明SLC1A2融合转录本的表达与一部分原发性CRC相关,可能有助于未来阐明SLC1A2融合阳性CRC的特征。