Department of Genetic Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205;
Department of Genetic Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Proc Natl Acad Sci U S A. 2020 Dec 22;117(51):32215-32222. doi: 10.1073/pnas.2019450117. Epub 2020 Dec 4.
Somatic LINE-1 (L1) retrotransposition has been detected in early embryos, adult brains, and the gastrointestinal (GI) tract, and many cancers, including epithelial GI tumors. We previously found numerous somatic L1 insertions in paired normal and GI cancerous tissues. Here, using a modified method of single-cell analysis for somatic L1 insertions, we studied adenocarcinomas of colon, pancreas, and stomach, and found a variable number of somatic L1 insertions in tumors of the same type from patient to patient. We detected no somatic L1 insertions in single cells of 5 of 10 tumors studied. In three tumors, aneuploid cells were detected by FACS. In one pancreatic tumor, there were many more L1 insertions in aneuploid than in euploid tumor cells. In one gastric cancer, both aneuploid and euploid cells contained large numbers of likely clonal insertions. However, in a second gastric cancer with aneuploid cells, no somatic L1 insertions were found. We suggest that when the cellular environment is favorable to retrotransposition, aneuploidy predisposes tumor cells to L1 insertions, and retrotransposition may occur at the transition from euploidy to aneuploidy. Seventeen percent of insertions were also present in normal cells, similar to findings in genomic DNA from normal tissues of GI tumor patients. We provide evidence that: 1) The number of L1 insertions in tumors of the same type is highly variable, 2) most somatic L1 insertions in GI cancer tissues are absent from normal tissues, and 3) under certain conditions, somatic L1 retrotransposition exhibits a propensity for occurring in aneuploid cells.
体细胞 LINE-1(L1)反转录转座已在早期胚胎、成人脑和胃肠道(GI)以及许多癌症中被检测到,包括上皮 GI 肿瘤。我们之前在配对的正常和 GI 癌组织中发现了大量体细胞 L1 插入。在这里,我们使用改良的体细胞 L1 插入单细胞分析方法,研究了结肠、胰腺和胃腺癌,发现来自同一患者的同类型肿瘤中的体细胞 L1 插入数量存在差异。我们在研究的 10 个肿瘤中的 5 个肿瘤的单细胞中没有检测到体细胞 L1 插入。在三个肿瘤中,通过 FACS 检测到非整倍体细胞。在一个胰腺肿瘤中,非整倍体肿瘤细胞中的 L1 插入数量明显多于整倍体肿瘤细胞。在一个胃癌中,非整倍体和整倍体细胞都含有大量可能的克隆插入。然而,在第二个含有非整倍体细胞的胃癌中,没有发现体细胞 L1 插入。我们认为,当细胞环境有利于反转录转座时,非整倍性使肿瘤细胞易于发生 L1 插入,并且反转录转座可能发生在从整倍体向非整倍体的转变过程中。17%的插入也存在于正常细胞中,与 GI 肿瘤患者正常组织基因组 DNA 的发现相似。我们提供的证据表明:1)同一类型肿瘤中的 L1 插入数量高度可变,2)GI 癌组织中的大多数体细胞 L1 插入不存在于正常组织中,3)在某些条件下,体细胞 L1 反转录转座倾向于发生在非整倍体细胞中。