Hosoda Kohei, Yashima Kazuo, Tamoto Akihiro, Yamamoto Sohei, Kawata Soichiro, Ikebuchi Yuichiro, Matsumoto Kazuya, Kawaguchi Koichiro, Harada Kenichi, Murawaki Yoshikazu, Isomoto Hajime
Division of Medicine and Clinical Science, Faculty of Medicine, Tottori University, Yonago, Tottori 683-8504, Japan.
Oncol Lett. 2017 Jul;14(1):737-742. doi: 10.3892/ol.2017.6196. Epub 2017 May 17.
Smoking and alcohol consumption are major risk factors for the development of esophageal squamous cell carcinoma (ESCC). Recent studies have demonstrated that smoking and alcohol consumption may be associated with altered DNA methylation in human cancer development. The aim of the present study was to evaluate methylation-modulated protein expression of tumor-related genes (TRGs) in the early stages of esophageal squamous neoplasia (ESN). ESN tissue samples (n=141) comprising 19 cases of low-grade intraepithelial neoplasia (LGIN), 70 of high-grade intraepithelial neoplasia/carcinoma (HGIN/CIS) and 52 of invasive cancer, were endoscopically resected. The methylation-modulated protein expression of 5 TRGs [fragile histidine triad (), E-cadherin, MutL homolog 1 () /MutS homolog 2 () and cyclooxygenase-2 ()] as well as was examined with immunohistochemistry, and their expression was compared with patient clinicopathological characteristics. Reduced or loss of FHIT, E-cadherin, MLH1/MSH2 and COX-2 expression was detected in 26.3 (5/19), 5.3 (1/19), 0 (0/19) and 63.2% (12/19) of LGIN cases, 61.4 (43/70), 18.6 (13/70), 7.1 (5/70) and 65.7% (46/70) of HGIN/CIS cases, and 78.8 (41/52), 50.0 (26/52), 11.5 (6/52) and 59.6% (31/52) of invasive cancer cases, respectively. Reduced or absent expression of FHIT and E-cadherin was significantly associated with neoplastic progression (FHIT, P=0.0007; E-cadherin, P=0.00014). The mean number of TRGs (/, and ) that exhibited reduced or absent expression in LGIN, HGIN/CIS and invasive cancer specimens was 1.12±0.61, 1.66±0.93 and 2.09±0.96, respectively, demonstrating a significant stepwise increment from LGIN to HGIN/CIS and then to invasive cancer (P<0.05). p53 overexpression was frequently detected in ESN with head and neck carcinomas. However p53 overexpression was not significantly associated with ESN progression. An increase in the number of the 5 TRG proteins with reduced or loss of expression in the early stages of esophageal tumorigenesis was demonstrated, and their decreased expression was observed to be associated with tumor progression. Therefore, smoking and alcohol drinking may be associated with not only carcinogenesis but also the progression of ESN.
吸烟和饮酒是食管鳞状细胞癌(ESCC)发生的主要危险因素。最近的研究表明,吸烟和饮酒可能与人类癌症发生过程中DNA甲基化的改变有关。本研究的目的是评估食管鳞状上皮瘤变(ESN)早期阶段肿瘤相关基因(TRGs)的甲基化调节蛋白表达。通过内镜切除了141例ESN组织样本,其中包括19例低级别上皮内瘤变(LGIN)、70例高级别上皮内瘤变/原位癌(HGIN/CIS)和52例浸润性癌。采用免疫组化方法检测了5种TRGs[脆性组氨酸三联体(FHIT)、E-钙黏蛋白、错配修复蛋白MutL同源物1(MLH1)/MutS同源物2(MSH2)和环氧化酶-2(COX-2)]以及p53的甲基化调节蛋白表达,并将其表达与患者临床病理特征进行比较。在LGIN病例中,FHIT、E-钙黏蛋白、MLH1/MSH2和COX-2表达降低或缺失的比例分别为26.3%(5/19)、5.3%(1/19)、0(0/19)和63.2%(12/19);在HGIN/CIS病例中分别为61.4%(43/70)、18.6%(13/70)、7.1%(5/70)和65.7%(46/70);在浸润性癌病例中分别为78.8%(41/52)、50.0%(?26/52)、11.5%(6/52)和59.6%(31/52)。FHIT和E-钙黏蛋白表达降低或缺失与肿瘤进展显著相关(FHIT,P = 0.0007;E-钙黏蛋白,P = 0.00014)。在LGIN、HGIN/CIS和浸润性癌标本中,表现出表达降低或缺失的TRGs(FHIT、MLH1和MSH2)的平均数量分别为1.12±0.61、1.66±0.93和2.09±0.96,显示出从LGIN到HGIN/CIS再到浸润性癌有显著的逐步增加(P<0.05)。p53过表达在伴有头颈部癌的ESN中经常被检测到。然而,p53过表达与ESN进展无显著相关性。在食管肿瘤发生早期,5种TRG蛋白表达降低或缺失的数量增加,且观察到它们的表达降低与肿瘤进展相关。因此,吸烟和饮酒可能不仅与致癌作用有关,还与ESN的进展有关。 (注:原文中“E-cadherin, MutL homolog 1 () /MutS homolog 2 () and cyclooxygenase-2 ()”括号内内容缺失,翻译时保留原文格式)