Literature DB >> 22249132

Overexpression of FOXM1 is associated with poor prognosis and clinicopathologic stage of pancreatic ductal adenocarcinoma.

Jin-Tang Xia1, Hua Wang, Li-Jian Liang, Bao-Gang Peng, Zhao-Feng Wu, Lian-Zhou Chen, Ling Xue, Zhi Li, Wen Li.   

Abstract

OBJECTIVES: Oncogenic transcription factor forkhead box M1 (FoxM1)-related clinicopathologic characteristics and prognosis of patients with pancreatic ductal adenocarcinoma (PDA) have not been identified. Our aim of studying FoxM1 expression level and survival rate of PDA is to determine whether FoxM1 is a valuable prognostic predictor for PDA patients.
METHODS: Expressional levels of FoxM1 mRNA and protein in paired pancreatic cancer lesions and adjacent noncancerous tissues were examined by reverse transcription-polymerase chain reaction and Western blotting. FoxM1 expression was analyzed by immunohistochemistry in 80 patients with PDA. The correlations between FoxM1 immunostaining levels and clinicopathologic factors, as well as the follow-up data of patients, were analyzed statistically.
RESULTS: FoxM1 protein and mRNA levels were elevated in pancreatic carcinoma lesions compared with the paired adjacent noncancerous tissues. A high level of expression of FoxM1 was significantly correlated with clinical staging (P = 0.004), lymph node metastasis (P = 0.009), and histological differentiation (P = 0.017). Patients with a higher FoxM1 expression had a significantly shorter survival time than those patients with lower FoxM1 expression (P < 0.001). The multivariate analysis revealed that FoxM1 could serve as an independent factor of poor prognosis.
CONCLUSIONS: Our finding indicates that FoxM1 could be used as prognostic molecular marker and therapeutic target for PDA.

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Year:  2012        PMID: 22249132     DOI: 10.1097/MPA.0b013e31823bcef2

Source DB:  PubMed          Journal:  Pancreas        ISSN: 0885-3177            Impact factor:   3.327


  34 in total

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Journal:  World J Gastroenterol       Date:  2014-08-21       Impact factor: 5.742

2.  FOXL1, a novel candidate tumor suppressor, inhibits tumor aggressiveness and predicts outcome in human pancreatic cancer.

Authors:  Geng Zhang; Peijun He; Jochen Gaedcke; B Michael Ghadimi; Thomas Ried; Harris G Yfantis; Dong H Lee; Nader Hanna; H Richard Alexander; S Perwez Hussain
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3.  FOXM1 promotes the warburg effect and pancreatic cancer progression via transactivation of LDHA expression.

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4.  FOXM1 and its oncogenic signaling in pancreatic cancer pathogenesis.

Authors:  Chen Huang; Jiawei Du; Keping Xie
Journal:  Biochim Biophys Acta       Date:  2014-01-11

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Journal:  Future Oncol       Date:  2016-03-17       Impact factor: 3.404

6.  Transcriptomic and CRISPR/Cas9 technologies reveal FOXA2 as a tumor suppressor gene in pancreatic cancer.

Authors:  Christina Vorvis; Maria Hatziapostolou; Swapna Mahurkar-Joshi; Marina Koutsioumpa; Jennifer Williams; Timothy R Donahue; George A Poultsides; Guido Eibl; Dimitrios Iliopoulos
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7.  UCHL3 promotes pancreatic cancer progression and chemo-resistance through FOXM1 stabilization.

Authors:  Zhiwang Song; Junhe Li; Ling Zhang; Jun Deng; Ziling Fang; Xiaojun Xiang; Jianping Xiong
Journal:  Am J Cancer Res       Date:  2019-09-01       Impact factor: 6.166

8.  High FOXM1 expression was associated with bladder carcinogenesis.

Authors:  Dongye Liu; Zhe Zhang; Chui-ze Kong
Journal:  Tumour Biol       Date:  2013-01-17

Review 9.  Targeting miRNAs for pancreatic cancer therapy.

Authors:  Min Shi; Dacheng Xie; Yong Gaod; Keping Xie
Journal:  Curr Pharm Des       Date:  2014       Impact factor: 3.116

10.  Overexpression of FoxM1 is associated with tumor progression in patients with clear cell renal cell carcinoma.

Authors:  Yi-Jun Xue; Ri-Hai Xiao; Da-Zhi Long; Xiao-Feng Zou; Xiao-Ning Wang; Guo-Xi Zhang; Yuan-Hu Yuan; Geng-Qing Wu; Jun Yang; Yu-Ting Wu; Hui Xu; Fo-Lin Liu; Min Liu
Journal:  J Transl Med       Date:  2012-09-24       Impact factor: 5.531

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