Han In Woong, Jang Jin-Young, Kwon Wooil, Park Taesung, Kim Yongkang, Lee Kyoung Bun, Kim Sun-Whe
Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Gangnam-Gu, Seoul 06351, Korea.
Department of Surgery and Cancer Research Institute, Seoul National University College of Medicine, Chongno-Gu, Seoul 110-744, Korea.
Oncotarget. 2017 Apr 25;8(17):29028-29037. doi: 10.18632/oncotarget.15995.
Bile duct cancer is one of the lethal cancers, presenting difficulties in early diagnosis and limited treatment modalities. Despite current advances in biomarker research, most studies have been performed in Western populations. Therefore, the purpose of this study was to determine a prognostic marker for bile duct cancer, especially in Korean patients, whose incidence of bile duct cancer is high.
Comparing cancer and normal bile duct tissue, we identified 29091 differentially expressed genes. CP, SCEL, and MUC16 had positive coefficients with a log2 ratio >1 for advanced T, N stage and perineural invasion cancer tissue. Strong immunohistochemical expression of ceruloplasmin was dominant in tumors with advanced T stage (p>0.999) and perineural invasion (p=0.316).
We performed tissue microarray experiment with 79 bile duct cancer tissue samples and 21 normal bile duct tissue samples. Candidate genes that has positive correlation with T, N stage and perineural invasion were drawn with multivariate analysis. Tissue expression of the genes was evaluated with an immunohistochemical study.
Ceruloplasmin is supposed to be related with advanced T stage and perineural invasion, having a possibility as a candidate prognostic marker for bile duct cancer.
胆管癌是致命性癌症之一,早期诊断困难且治疗方式有限。尽管目前生物标志物研究取得了进展,但大多数研究是在西方人群中进行的。因此,本研究的目的是确定胆管癌的预后标志物,尤其是在胆管癌发病率较高的韩国患者中。
通过比较癌组织和正常胆管组织,我们鉴定出29091个差异表达基因。CP、SCEL和MUC16在晚期T、N期及神经周围浸润癌组织中具有正系数,log2比值>1。铜蓝蛋白的强免疫组化表达在晚期T期肿瘤(p>0.999)和神经周围浸润(p=0.316)中占主导地位。
我们对79个胆管癌组织样本和21个正常胆管组织样本进行了组织芯片实验。通过多变量分析得出与T、N期及神经周围浸润呈正相关的候选基因。通过免疫组化研究评估这些基因的组织表达。
铜蓝蛋白被认为与晚期T期和神经周围浸润有关,有可能作为胆管癌的候选预后标志物。