scholarly journals Alpha-l-fucosidase: a novel serum biomarker to predict prognosis in early stage esophageal squamous cell carcinoma

2019 ◽  
Vol 11 (9) ◽  
pp. 3980-3990 ◽  
Author(s):  
Xiangyang Yu ◽  
Rusi Zhang ◽  
Tianzhen Yang ◽  
Mengqi Zhang ◽  
Kexing Xi ◽  
...  
BMC Cancer ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Xiaofeng Duan ◽  
Xiaobin Shang ◽  
Jie Yue ◽  
Zhao Ma ◽  
Chuangui Chen ◽  
...  

Abstract Background A nomogram was developed to predict lymph node metastasis (LNM) for patients with early-stage esophageal squamous cell carcinoma (ESCC). Methods We used the clinical data of ESCC patients with pathological T1 stage disease who underwent surgery from January 2011 to June 2018 to develop a nomogram model. Multivariable logistic regression was used to confirm the risk factors for variable selection. The risk of LNM was stratified based on the nomogram model. The nomogram was validated by an independent cohort which included early ESCC patients underwent esophagectomy between July 2018 and December 2019. Results Of the 223 patients, 36 (16.1%) patients had LNM. The following three variables were confirmed as LNM risk factors and were included in the nomogram model: tumor differentiation (odds ratio [OR] = 3.776, 95% confidence interval [CI] 1.515–9.360, p = 0.004), depth of tumor invasion (OR = 3.124, 95% CI 1.146–8.511, p = 0.026), and tumor size (OR = 2.420, 95% CI 1.070–5.473, p = 0.034). The C-index was 0.810 (95% CI 0.742–0.895) in the derivation cohort (223 patients) and 0.830 (95% CI 0.763–0.902) in the validation cohort (80 patients). Conclusions A validated nomogram can predict the risk of LNM via risk stratification. It could be used to assist in the decision-making process to determine which patients should undergo esophagectomy and for which patients with a low risk of LNM, curative endoscopic resection would be sufficient.


2019 ◽  
Vol 89 (6) ◽  
pp. AB576-AB577
Author(s):  
Sophie L. Brigstocke ◽  
Vaishali Patel ◽  
Saurabh Chawla ◽  
Parit Mekaroonkamol ◽  
Steven Keilin ◽  
...  

2013 ◽  
Vol 27 (2) ◽  
pp. 171-186 ◽  
Author(s):  
Michio Shimizu ◽  
Giovanni Zaninotto ◽  
Koji Nagata ◽  
David Y. Graham ◽  
Gregory Y. Lauwers

Esophagus ◽  
2016 ◽  
Vol 13 (3) ◽  
pp. 245-253 ◽  
Author(s):  
Youichi Kumagai ◽  
Jun Sobajima ◽  
Morihiro Higashi ◽  
Toru Ishiguro ◽  
Minoru Fukuchi ◽  
...  

Esophagus ◽  
2011 ◽  
Vol 9 (1) ◽  
pp. 33-38 ◽  
Author(s):  
Makoto Hikage ◽  
Takashi Kamei ◽  
Fumiyoshi Fujishima ◽  
Go Miyata ◽  
Ko Onodera ◽  
...  

Esophagus ◽  
2017 ◽  
Vol 15 (1) ◽  
pp. 19-26 ◽  
Author(s):  
Youichi Kumagai ◽  
Tetsuhiko Tachikawa ◽  
Morihiro Higashi ◽  
Jun Sobajima ◽  
Akemi Takahashi ◽  
...  

2020 ◽  
Author(s):  
Xiuqin Wei ◽  
Qiang Gao ◽  
Wei Jia ◽  
Chao Ma ◽  
Mei Xue ◽  
...  

Abstract BACKGROUND: Esophageal squamous cell carcinoma (ESCC) in some cases can be diagnosed as esophageal varices (EV). DLG1-AS1 promotes cervical cancer, while its function is other malignancies remains unknown. Our aim for this study is to study the role of DLG1-AS1 in esophageal squamous cell carcinoma.METHODS: Plasma levels of DLG1-AS1 in 66 early stage ESCC patients, 60 EV patients and 60 healthy controls were measured by RT-qPCR. Receiver operating characteristic (ROC) curve was applied to analyze the diagnostic value of DLG1-AS1 for early stage ESCC. Relationship between miR-145 and DLG1-AS1 was analyzed by overexpression experiments. Proliferation of cells was determined by CCK-8 assay. RESULTS: DLG1-AS1 was upregulated in ESCC, but not in EV patients compared with healthy control. DLG1-AS1 overexpression distinguished ESCC patients from healthy controls and EV patients. Plasma miR-145 was inversely correlated with DLG1-AS1 in ESCC patients. Moreover, DLG1-AS1 overexpression resulted in the downregulation of miR-145, while miR-145 mimic transfection did not significantly alter DLG1-AS1. Overexpression of DLG1-AS1 mediated the promoted, while overexpression of miR-145 resulted in inhibited proliferation of ESCC cells. The role of DLG1-AS1 overexpression was inhibited by miR-145 mimic transfection. CONCLUSION: Therefore, DLG1-AS1 may promote ESCC under the repression of miR-145.


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