Department of Gastroenterology, Faculty of Medicine, Yamagata University, 2-2-2 Iida-Nishi, Yamagata, 990-9585, Japan.
Division of Endoscopy, Yamagata University Hospital, 2-2-2 Iida-Nishi, Yamagata, 990-9585, Japan.
Sci Rep. 2021 Oct 11;11(1):20150. doi: 10.1038/s41598-021-99790-z.
Alcohol consumption and smoking pose a significant risk for esophageal squamous cell neoplasia (ESCN) development in males; however, ESCN is often diagnosed in non-drinking and non-smoking females. The mechanisms underlying these differences remain elusive, and understanding them can potentially identify novel pathways involved in ESCN development. We performed short-read sequencing to identify somatic variants on a cancer panel targeting 409 genes using DNA extracted from the superficial squamous cell carcinoma (ESCC) tissues and adjacent non-neoplastic epithelium (NE), and immunohistochemical staining of the protein encoded by the target gene. All male patients (n = 117) were drinkers or smokers, whereas 45% of the female patients (n = 33) were not. Somatic variants were compared among three age-matched groups: 13 female ESCC patients with smoking and drinking habits (known-risk group, F-KR), 13 female ESCC patients without these habits (unknown-risk group, F-UR), and 27 males with ESCC and smoking and drinking habits (M-KR). In the NE, the frequencies of CDKN2A variants were significantly higher in F-UR than in F-KR and M-KR. In both ESCC and NE, p14ARF was significantly overexpressed in F-UR than in the other groups. In conclusion, CDKN2A might be important in ESCC development, independent of known risk factors.
饮酒和吸烟会增加男性患食管鳞状细胞癌(ESCN)的风险;然而,在不饮酒和不吸烟的女性中,ESCN 也经常被诊断出来。这些差异的潜在机制尚不清楚,而了解这些机制可能有助于确定 ESCN 发展过程中的新途径。我们使用从浅表性鳞状细胞癌(ESCC)组织和相邻非肿瘤上皮(NE)中提取的 DNA,对靶向 409 个基因的癌症面板进行短读测序,以鉴定体细胞变异,并用目标基因编码的蛋白质进行免疫组织化学染色。所有男性患者(n=117)均为饮酒或吸烟者,而 45%的女性患者(n=33)没有这些习惯。我们比较了三组年龄匹配的患者的体细胞变异:13 名有吸烟和饮酒习惯的女性 ESCC 患者(已知风险组,F-KR)、13 名没有这些习惯的女性 ESCC 患者(未知风险组,F-UR)和 27 名有吸烟和饮酒习惯的男性 ESCC 患者(M-KR)。在 NE 中,F-UR 组 CDKN2A 变异的频率明显高于 F-KR 和 M-KR 组。在 ESCC 和 NE 中,p14ARF 在 F-UR 中的表达明显高于其他组。总之,CDKN2A 可能是 ESCC 发展的重要因素,独立于已知的危险因素。