Boottanun Patcharaporn, Ino Yoshinori, Shimada Kazuaki, Hiraoka Nobuyoshi, Angata Kiyohiko, Narimatsu Hisashi
Graduate School of Comprehensive Human Sciences, Major in Medical Sciences, Clinical Sciences Program, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.
Molecular and Cellular Glycoproteomics Research Group, Department of Life Science and Biotechnology, Cellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki 305-8565, Japan.
Oncol Lett. 2021 Nov;22(5):760. doi: 10.3892/ol.2021.13021. Epub 2021 Sep 3.
Cholangiocarcinoma (CCA) is a highly aggressive and metastatic type of malignant carcinoma that is associated with high mortality rates and is difficult to detect at early stages. Core 3 structure is a mucin-type -glycans synthesized by β1,3--acetylglucosaminyltransferase 6 (core 3 synthase), which plays an important role in the digestive system, in particular gastrointestinal goblet cells. It has been reported that core 3 synthase-expressing cells show lower migratory and invasive rates, and lower metastatic activity. A immunohistochemical study also showed that this enzyme was expressed in normal epithelial cells of the colon, but completely disappeared in colorectal cancer cells. The present study aimed to identify biomarkers that could be used to predict the prognosis of patients with CCA. Pathological specimens of 185 CCA tissues were immunohistochemically stained with two antibodies, G8-144 and MECA-79, which recognize core 3 synthase and 6-sulfated -acetyllactosamine on the extended core-1 -glycans, respectively. The association between G8-144 or MECA-79 positivity and patient prognosis was statistically analyzed. Positive expression of G8-144 was associated with improved prognosis in patients with distal CCA (dCCA). Patients with dCCA positive for G8-144 showed lower mortality rates than those with negative expression. However, the positive expression of MECA-79 was associated with CCA progression and metastasis, indicating that it is a poor prognostic marker for CCA. In conclusion, as both antibodies resulted in mirror-image staining, the involvement of G8-144 and MECA-79 in -glycan synthesis could be considered as potential favorable and unfavorable biomarkers, respectively, for CCA prognosis.
胆管癌(CCA)是一种具有高度侵袭性和转移性的恶性肿瘤,死亡率高,且早期难以检测。核心3结构是一种由β1,3-N-乙酰氨基葡萄糖转移酶6(核心3合酶)合成的粘蛋白型聚糖,在消化系统尤其是胃肠道杯状细胞中起重要作用。据报道,表达核心3合酶的细胞迁移和侵袭率较低,转移活性也较低。一项免疫组织化学研究还表明,这种酶在结肠正常上皮细胞中表达,但在结肠癌细胞中完全消失。本研究旨在确定可用于预测CCA患者预后的生物标志物。用两种抗体G8-144和MECA-79对185例CCA组织的病理标本进行免疫组织化学染色,这两种抗体分别识别核心3合酶和延伸核心1聚糖上的6-硫酸化N-乙酰乳糖胺。对G8-144或MECA-79阳性与患者预后之间的关联进行统计学分析。G8-144的阳性表达与远端CCA(dCCA)患者预后改善相关。G8-144阳性的dCCA患者死亡率低于阴性表达患者。然而,MECA-79的阳性表达与CCA进展和转移相关,表明它是CCA的不良预后标志物。总之,由于两种抗体染色结果呈镜像,G8-144和MECA-79参与聚糖合成可分别被视为CCA预后潜在的有利和不利生物标志物。