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Cyclin A1 is associated with poor prognosis in oesophageal squamous cell carcinoma

  • Authors:
    • Xiaoting He
    • Suqing Li
    • Weihong Shi
    • Qingfeng Lin
    • Jian Ma
    • Yang Liu
    • Tingting Feng
    • Xiufeng Cao
  • View Affiliations / Copyright

    Affiliations: Department of Surgical Oncology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu 210000, P.R. China, Department of Clinical Medicine, Yancheng Vocational Institute of Health Sciences, Yancheng, Jiangsu 224005, P.R. China, Department of Medical Oncology, Jiangyin People's Hospital, Jiangyin, Jiangsu 214400, P.R. China, Department of Pharmacy, No. 401 Hospital of Chinese People's Liberation Army, Qingdao, Shandong 266071, P.R. China, Institute of Biology and Medical Sciences, Soochow University, Suzhou, Jiangsu 215123, P.R. China
    Copyright: © He et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 706-712
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    Published online on: May 20, 2019
       https://doi.org/10.3892/ol.2019.10377
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Abstract

Dysregulation of cyclin A1 (CCNA1) is implicated in the carcinogenesis, progression and metastasis of many types of solid tumours. In the present study, an mRNA single‑channel expression profile chip experiment revealed that the CCNA1 mRNA levels in oesophageal squamous cell carcinoma (ESCC) were increased >10‑fold compared with those in the adjacent non‑cancer tissues. Reverse transcription‑quantitative polymerase chain reaction and immunohistochemistry analyses were performed to additionally investigate the role of CCNA1 in the development and progression of ESCC in patients treated by radical resection of the oesophagus. The association between CCNA1 mRNA expression and the clinicopathological parameters of patients with ESCC was statistically analysed. The results indicated that upregulation of CCNA1 occurred in ~70% of patients with ESCC, and increased CCNA1 mRNA expression was significantly associated with advanced clinical stage, lymph node metastasis, invasiveness and poor clinical outcome, including disease‑free survival and overall survival rates. Taken together, the data suggested that CCNA1 had an important function in ESCC development and progression, and may serve as a prognostic biomarker and therapeutic target in ESCC.
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Copy and paste a formatted citation
Spandidos Publications style
He X, Li S, Shi W, Lin Q, Ma J, Liu Y, Feng T and Cao X: Cyclin A1 is associated with poor prognosis in oesophageal squamous cell carcinoma. Oncol Lett 18: 706-712, 2019.
APA
He, X., Li, S., Shi, W., Lin, Q., Ma, J., Liu, Y. ... Cao, X. (2019). Cyclin A1 is associated with poor prognosis in oesophageal squamous cell carcinoma. Oncology Letters, 18, 706-712. https://doi.org/10.3892/ol.2019.10377
MLA
He, X., Li, S., Shi, W., Lin, Q., Ma, J., Liu, Y., Feng, T., Cao, X."Cyclin A1 is associated with poor prognosis in oesophageal squamous cell carcinoma". Oncology Letters 18.1 (2019): 706-712.
Chicago
He, X., Li, S., Shi, W., Lin, Q., Ma, J., Liu, Y., Feng, T., Cao, X."Cyclin A1 is associated with poor prognosis in oesophageal squamous cell carcinoma". Oncology Letters 18, no. 1 (2019): 706-712. https://doi.org/10.3892/ol.2019.10377
Copy and paste a formatted citation
x
Spandidos Publications style
He X, Li S, Shi W, Lin Q, Ma J, Liu Y, Feng T and Cao X: Cyclin A1 is associated with poor prognosis in oesophageal squamous cell carcinoma. Oncol Lett 18: 706-712, 2019.
APA
He, X., Li, S., Shi, W., Lin, Q., Ma, J., Liu, Y. ... Cao, X. (2019). Cyclin A1 is associated with poor prognosis in oesophageal squamous cell carcinoma. Oncology Letters, 18, 706-712. https://doi.org/10.3892/ol.2019.10377
MLA
He, X., Li, S., Shi, W., Lin, Q., Ma, J., Liu, Y., Feng, T., Cao, X."Cyclin A1 is associated with poor prognosis in oesophageal squamous cell carcinoma". Oncology Letters 18.1 (2019): 706-712.
Chicago
He, X., Li, S., Shi, W., Lin, Q., Ma, J., Liu, Y., Feng, T., Cao, X."Cyclin A1 is associated with poor prognosis in oesophageal squamous cell carcinoma". Oncology Letters 18, no. 1 (2019): 706-712. https://doi.org/10.3892/ol.2019.10377
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