Department of Biochemistry and Molecular Biology, Institute of Pathology and Pathophysiology, College of Basic Medicine, China Medical University, Shenyang, China.
Histol Histopathol. 2013 Sep;28(9):1147-56. doi: 10.14670/HH-28.1147. Epub 2013 Apr 4.
Bcl-2-associated athanogene 3 (Bag-3) belongs to a member of the Hsc70 binding co-chaperone Bag-family proteins and has critical roles in protein homeostasis, cell survival, actin organization, cell adhesion, cell motility and tumor metastasis. To clarify the role of Bag-3 in colorectal carcinogenesis and subsequent development, its expression was examined by immunohistochemistry (IHC) and in situ hybridization (ISH) on tissue microarrays containing colorectal carcinomas, adenomas, non-neoplastic mucosa (NNM) and metastatic carcinomas in lymph node and liver. Colorectal carcinoma tissue and cell lines were studied for Bag-3 expression by RT-PCR, Western blot and immunofluorescence. The results demonstrated that Bag3 was distinctly expressed in Colo201, Colo205, DLD-1, HCT-15, HCT-116, HT-29, KM-12, SW480, SW620, and WiDr at both mRNA and protein levels. Carcinoma showed stronger Bag-3 expression than adjacent NNM by IHC and Western blot (P<0.05), while its mRNA had the opposite by real-time PCR and ISH (P<0.05). Metastatic carcinoma more frequently expressed Bag-3 mRNA in lymph node and liver than in primary carcinoma (P<0.05). Immunohistochemically, Bag-3 expression was seen to gradually decrease from carcinoma, adenoma to NNM (P<0.05). There was a positive correlation between Bag-3 expression and TNM staging and GRP94 expression (P<0.05), but no relationship to patient age or sex, tumor size, depth of invasion, lymphatic or venous invasion, lymph node metastasis, differentiation or prognosis of colorectal carcinomas (P<0.05). Our study indicated that aberrant Bag-3 expression might be involved in colorectal adenoma-adenocarcinoma sequence and subsequent progression.
Bcl-2 相关抗凋亡基因 3(Bag-3)属于 Hsc70 结合伴侣蛋白 Bag 家族蛋白的成员,在蛋白质稳态、细胞存活、肌动蛋白组织、细胞黏附、细胞运动和肿瘤转移中发挥关键作用。为了阐明 Bag-3 在结直肠癌发生和随后发展中的作用,我们通过免疫组织化学(IHC)和组织微阵列中的原位杂交(ISH)检查了其表达,该微阵列包含结直肠癌、腺瘤、非肿瘤性黏膜(NNM)和淋巴结和肝脏中的转移性癌。通过 RT-PCR、Western blot 和免疫荧光研究了结直肠癌组织和细胞系中的 Bag-3 表达。结果表明,在 Colo201、Colo205、DLD-1、HCT-15、HCT-116、HT-29、KM-12、SW480、SW620 和 WiDr 中,Bag3 在 mRNA 和蛋白水平上均有明显表达。与相邻的 NNM 相比,IHC 和 Western blot 显示癌组织中 Bag-3 的表达更强(P<0.05),而实时 PCR 和 ISH 显示其 mRNA 表达相反(P<0.05)。淋巴结和肝脏中的转移性癌比原发性癌更频繁地表达 Bag-3 mRNA(P<0.05)。免疫组织化学显示,Bag-3 的表达从癌、腺瘤到 NNM 逐渐降低(P<0.05)。Bag-3 的表达与 TNM 分期和 GRP94 表达呈正相关(P<0.05),但与患者年龄、性别、肿瘤大小、浸润深度、淋巴或静脉浸润、淋巴结转移、分化或结直肠癌的预后无关(P<0.05)。我们的研究表明,异常的 Bag-3 表达可能参与了结直肠腺瘤-腺癌序列和随后的进展。