Department of Thyroid and Breast Surgery, Northern Jiangsu People's Hospital and Clinical Medical College of Yangzhou University, No.98 Nantong West Road, Yangzhou, 225001, China.
Departments of CyberKnife, Huashan Hospital, Fudan University, No.525,Hongfeng Road, Shanghai, 200032, China.
Cell Commun Signal. 2018 Feb 20;16(1):8. doi: 10.1186/s12964-018-0219-0.
High-mobility group box 2 (HMGB2) is implicated in tumorigenesis in various cancers. However, the clinical significance of HMGB2 signaling in human breast cancer progression remains unknown.
We investigated HMGB2 expression in 185 cases of primary breast cancer and matched normal breast tissue specimens, and explored the underlying mechanisms of altered HMGB2 expression as well as the impact of this altered expression on breast cancer growth and on aerobic glycolysis using in vitro and animal models of breast cancer.
HMGB2 was more highly expressed in tumor-cell nuclei of breast cancer cells than in the adjacent normal breast tissues (P < 0.05). Higher HMGB2 expression correlated with larger tumor size (P = 0.003) and advanced tumor stage (P = 0.033). A Cox proportional hazards model revealed that HMGB2 expression was an independent prognostic factor for breast cancer after radical resection (P < 0.05). Experimentally, knockdown of HMGB2 expression by stable transfected shRNA significantly decreased the growth and glycolysis of breast cancer cells both in vitro and in mouse models. Mechanically, promotion of breast cancer progression by HMGB2 directly and significantly correlated with activation of LDHB expression and inactivation of FBP1 expression.
These results disclose a novel role for HMGB2 in reprogramming the metabolic process in breast cancer cells by targeting LDHB and FBP1 and provide potential prognostic predictors for breast cancer patients.
高迁移率族蛋白 B2(HMGB2)参与多种癌症的发生。然而,HMGB2 信号在人乳腺癌进展中的临床意义尚不清楚。
我们研究了 185 例原发性乳腺癌和匹配的正常乳腺组织标本中 HMGB2 的表达,并用体外和乳腺癌动物模型探索了 HMGB2 表达改变的潜在机制以及这种改变对乳腺癌生长和有氧糖酵解的影响。
HMGB2 在乳腺癌细胞核中的表达高于相邻的正常乳腺组织(P<0.05)。较高的 HMGB2 表达与较大的肿瘤大小(P=0.003)和较晚期的肿瘤分期相关(P=0.033)。Cox 比例风险模型显示,HMGB2 表达是根治性切除后乳腺癌的独立预后因素(P<0.05)。实验上,通过稳定转染 shRNA 敲低 HMGB2 表达显著降低了乳腺癌细胞在体外和小鼠模型中的生长和糖酵解。机制上,HMGB2 通过直接和显著地上调 LDHB 表达和下调 FBP1 表达促进乳腺癌的进展。
这些结果揭示了 HMGB2 通过靶向 LDHB 和 FBP1 重编程乳腺癌细胞代谢过程的新作用,并为乳腺癌患者提供了潜在的预后预测因子。