He Jing, Yao Youyuan, Quan Fei, Lu Zhongyu, Wang Jian, Gao Wen
Medical Oncology Department, Jiangsu Province Hospital, Nanjing, Jiangsu, 210029, People's Republic of China.
The Medical Department, Jiangsu Simcere Diagnostics Co., Ltd, Nanjing, Jiangsu, 210021, People's Republic of China.
Onco Targets Ther. 2023 Jul 7;16:535-540. doi: 10.2147/OTT.S406234. eCollection 2023.
Intergenic-gene fusion detected by DNA-seq is particularly confusing for drug selection since the function of the intergenic region located upstream is unknown. We reported a case of a 49-year-old male with advanced lung adenocarcinoma, who was detected FBXO11 (intergenic)-ALK (exon 20-29) by DNA-seq, and FISH analysis revealed a positive result. The patient was treated with crizotinib and achieved a PR. The canonical EML4 (exon 1-13)-ALK (exon 20-29) fusion verified by RNA-seq suggested a complex EML4 (exon 1-13)-FBXO11 (intergenic)-ALK (exon 20-29) tripartite rearrangement at the DNA level. Our case emphasized the necessity of RNA-seq for verifying intergenic-gene fusion. Simultaneously, the pathogenic germline SLX4 variant and extensive CNVs of DNA segment were detected by DNA-seq deserves our attention.
通过DNA测序检测到的基因间基因融合对于药物选择来说尤其令人困惑,因为位于上游的基因间区域的功能尚不清楚。我们报告了一例49岁晚期肺腺癌男性病例,通过DNA测序检测到FBXO11(基因间)-ALK(外显子20-29),荧光原位杂交分析结果呈阳性。该患者接受克唑替尼治疗并获得部分缓解。RNA测序验证的经典EML4(外显子1-13)-ALK(外显子20-29)融合表明在DNA水平上存在复杂的EML4(外显子1-13)-FBXO11(基因间)-ALK(外显子20-29)三方重排。我们的病例强调了RNA测序对于验证基因间基因融合的必要性。同时,通过DNA测序检测到的致病性种系SLX4变异和DNA片段的广泛拷贝数变异值得我们关注。