Carcinogenesis, Teratogenesis & Mutagenesis ›› 2020, Vol. 32 ›› Issue (3): 161-165.doi: 10.3969/j.issn.1004-616x.2020.03.001

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Expression status of p-mTOR and its prognostic implication in colorectal cancer

ZHU Yiqing1, ZHANG Tongtong1,2, ZHENG Junwen1, HAO Jiajie1, CAI Yan1, WANG Mingrong1, LIANG Jianwei3, ZHANG Yu1   

  1. 1. State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021;
    2. Medical Research Center, The Third People's Hospital of Chengdu, Chengdu 610031, Sichuan;
    3. Department of Colorectal Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China
  • Received:2020-01-13 Revised:2020-04-11 Online:2020-05-31 Published:2020-06-03

Abstract: OBJECTIVE: To investigate expression status of p-mTOR(Ser2448,an active form of mTOR)in colorectal cancer (CRC),and its correlation with clinicopathological features and prognosis. METHODS: Protein expression of p-mTOR was examined using the tissue microarrays-immunohistochemistry (TMA-IHC) technique in surgically-resected colorectal cancer tissues and adjacent normal epithelia from 441 patients. Correlations between p-mTOR expression levels,clinicopathological parameters and prognosis of patients were analyzed using the Pearson Chi-square and Fisher exact tests,and Kaplan-Meier survival and Cox regression analyses. RESULTS: Overexpression of p-mTOR was detected in 58% (254/441) of the CRC specimens but only 4% (17/441) of the normal colorectal epithelia,and the difference between them was significant (P < 0.01). In addition,elevated p-mTOR expression was positively correlated with higher pathologic T stage,lymph node metastasis,distant metastasis,and advanced clinical stage (each P < 0.05). Kaplan-Meier survival analysis showed the expression level of p-mTOR was significantly correlated with the poor prognosis of colorectal cancer patients (each P < 0.05). The disease-free survival (DFS) and overall survival (OS) of patients with high expression of p-mTOR were 52 and 60 months,respectively,which were significantly shorter than those with low expression of p-mTOR (71 and 70 months). The Cox multiple regression analyses reveal that p-mTOR overexpression was an independent prognostic factor for DFS and OS in CRC patients. CONCLUSION: p-mTOR was frequently upregulated in CRC,and its overexpression was significantly correlated with adverse outcomes;thus,it may serve as a potential prognostic marker for predicting the risk of postoperative death,recurrence and metastasis in patients with colorectal cancer.

Key words: colorectal cancer, phospho-mammalian/mechanistic target of rapamycin, prognostic biomarker, disease-free survival rate, overall survival rate

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