Honjo Hiroaki, Toh Yasushi, Sohda Makoto, Suzuki Shigemasa, Kaira Kyoichi, Kanai Yoshikatsu, Nagamori Shushi, Oyama Tetsunari, Yokobori Takehiko, Miyazaki Tatsuya, Kuwano Hiroyuki
Department of General Surgical Science, Gunma University, Graduate School of Medicine, Gunma, Japan
Department of Gastroenterological Surgery, National Kyushu Cancer Center, Fukuoka, Japan.
Anticancer Res. 2017 Aug;37(8):4147-4155. doi: 10.21873/anticanres.11802.
BACKGROUND/AIM: Metastasis-associated gene 1 (MTA1) is considered a potential prognostic factor in esophageal cancer. We investigated the clinical relationship between MTA1, LAT1, and tumor metabolism, as evaluated by positron emission tomography (PET) in esophageal squamous cell carcinoma.
We analyzed 142 esophageal squamous cell carcinoma patients who underwent curative resection without preoperative treatment. MTA1 expression was assessed by immuno-zahistochemistry, and tested against standardized uptake values from preoperative PET-CT. The association among MTA1, LAT1, and FAMT PET results were analyzed.
MTA1 staining was observed in 82 of 142 cancer tissues. Five-year overall survival was 69.9 % in the absence of MTA1, but 50.7% otherwise (p=0.021), while disease-free survival was 66.5% and 49.0% (p=0.071), respectively. Abnormal FAMT accumulation was noted in 13 patients without MTA1 and in 18 patients with MTA1 (p=0.079), with maximum standardized uptake value 1.6±1.6 and 2.7±1.6, respectively (p=0.036). MTA1 expression was positively correlated with LAT1 (p=0.013) and CD34 (p=0.034) expression, but not with Ki-67 (p=0.078).
MTA1 shows promise as a diagnostic and prognostic marker in esophageal cancer, and we anticipate that the gene will also prove to be a good therapeutic target.
背景/目的:转移相关基因1(MTA1)被认为是食管癌潜在的预后因素。我们研究了MTA1、LAT1与肿瘤代谢之间的临床关系,通过正电子发射断层扫描(PET)评估食管鳞状细胞癌。
我们分析了142例未接受术前治疗而行根治性切除术的食管鳞状细胞癌患者。通过免疫组织化学评估MTA1表达,并与术前PET-CT的标准化摄取值进行对比。分析MTA1、LAT1和FAMT PET结果之间的关联。
142例癌组织中有82例观察到MTA1染色。无MTA1者的5年总生存率为69.9%,否则为50.7%(p=0.021),而无病生存率分别为66.5%和49.0%(p=0.071)。13例无MTA1的患者和18例有MTA1的患者出现异常FAMT蓄积(p=0.079),最大标准化摄取值分别为1.6±1.6和2.7±1.6(p=0.036)。MTA1表达与LAT1(p=0.013)和CD34(p=0.034)表达呈正相关,但与Ki-67无关(p=0.078)。
MTA1有望成为食管癌的诊断和预后标志物,我们预计该基因也将被证明是一个良好的治疗靶点。