Chen Zhiao, Lu Xinyuan, Wang Zhichao, Jin Guangzhi, Wang Qifeng, Chen Di, Chen Taoyang, Li Jinjun, Fan Jia, Cong Wenming, Gao Qiang, He Xianghuo
Fudan University Shanghai Cancer Center and Institutes of Biomedical Sciences, Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Department of Pathology, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Oncotarget. 2015 Feb 10;6(4):2538-48. doi: 10.18632/oncotarget.2991.
The identification of prognostic markers for hepatocellular carcinoma (HCC) is needed for clinical practice. Tripartite motif-containing 35 (TRIM35) is a tumor suppressor of HCC. TRIM35 inhibits phosphorylation of pyruvate kinase isoform M2 (PKM2), which is involved in aerobic glycolysis of cancer cells. We found that expression of PKM2 was significantly increased in HCC tissues. This overexpression of PKM2 was correlated with a high TNM stage and level of vascular invasion. Patients with HCC who were positive for PKM2 expression and negative for TRIM35 expression had shorter overall survival and time to recurrence than patients who were negative for PKM2 and positive for TRIM35. Furthermore, PKM2/TRIM35 combination was an independent and significant risk factor for recurrence and survival. In conclusion, PKM2 (+) and TRIM35 (-) contribute to the aggressiveness and poor prognosis of HCC. PKM2/TRIM35 expression could be a biomarker for the prognosis of HCC and target for cancer therapy.
临床实践需要确定肝细胞癌(HCC)的预后标志物。含三联基序蛋白35(TRIM35)是HCC的一种肿瘤抑制因子。TRIM35抑制丙酮酸激酶M2亚型(PKM2)的磷酸化,PKM2参与癌细胞的有氧糖酵解。我们发现PKM2在HCC组织中的表达显著增加。PKM2的这种过表达与高TNM分期和血管侵犯程度相关。PKM2表达阳性且TRIM35表达阴性的HCC患者的总生存期和复发时间比PKM2阴性且TRIM35阳性的患者短。此外,PKM2/TRIM35组合是复发和生存的独立且显著的危险因素。总之,PKM2(+)和TRIM35(-)导致HCC的侵袭性和不良预后。PKM2/TRIM35表达可能是HCC预后的生物标志物和癌症治疗的靶点。