scholarly journals Cytokeratin-based assessment of tumour budding in colorectal cancer: analysis in stage II patients and prospective diagnostic experience

2017 ◽  
Vol 3 (3) ◽  
pp. 171-178 ◽  
Author(s):  
Viktor H Koelzer ◽  
Naziheh Assarzadegan ◽  
Heather Dawson ◽  
Bojana Mitrovic ◽  
Andrea Grin ◽  
...  
2015 ◽  
Vol 46 (3) ◽  
pp. 212-218 ◽  
Author(s):  
F. Petrelli ◽  
E. Pezzica ◽  
M. Cabiddu ◽  
A. Coinu ◽  
K. Borgonovo ◽  
...  

2018 ◽  
Vol 5 (1) ◽  
pp. 63-78 ◽  
Author(s):  
Khadija Slik ◽  
Sami Blom ◽  
Riku Turkki ◽  
Katja Välimäki ◽  
Samu Kurki ◽  
...  

2019 ◽  
Vol 74 (7) ◽  
pp. 1005-1013 ◽  
Author(s):  
Masato Yamadera ◽  
Eiji Shinto ◽  
Yoshiki Kajiwara ◽  
Satsuki Mochizuki ◽  
Koichi Okamoto ◽  
...  

2020 ◽  
Vol 14 ◽  
Author(s):  
Augusto Leite Canguçu ◽  
Ediel Valério ◽  
Roberto Bonfim Pimenta Peixoto ◽  
Tiago Cordeiro Felismino ◽  
Celso Abdon Lopes de Mello ◽  
...  

2019 ◽  
Vol 65 (5) ◽  
pp. 701-707
Author(s):  
Vitaliy Shubin ◽  
Yuriy Shelygin ◽  
Sergey Achkasov ◽  
Yevgeniy Rybakov ◽  
Aleksey Ponomarenko ◽  
...  

To determine mutations in the plasma KRAS gene in patients with colorectal cancer was the aim of this study. The material was obtained from 44 patients with colorectal cancer of different stages (T1-4N0-2bM0-1c). Plasma for the presence of KRAS gene mutation in circulating tumor DNA was investigated using digital droplet polymerase chain reaction (PCR). KRAS mutations in circulating tumor DNA isolated from 1 ml of plasma were detected in 13 (30%) patients with cancer of different stages. Of these, with stage II, there were 3 patients, with III - 5 and with IV - 5. Patients who did not have mutations in 1 ml of plasma were analyzed for mutations of KRAS in circulating tumor DNA isolated from 3 ml of plasma. Five more patients with KRAS mutations were found with II and III stages. The highest concentrations of circulating tumor DNA with KRAS mutation were found in patients with stage IV. The increase in plasma volume to 3 ml did not lead to the identification of mutations in I stage. This study showed that digital droplet PCR allows identification of circulating tumor DNA with the KRAS mutations in patients with stage II-IV of colon cancer. The results can be used to determine the degree of aggressiveness of the tumor at different stages of the disease, but not the 1st, and it is recommended to use a plasma volume of at least 3 ml.


2020 ◽  
Vol 14 (12) ◽  
pp. 1127-1137
Author(s):  
Tong-Tong Zhang ◽  
Yi-Qing Zhu ◽  
Hong-Qing Cai ◽  
Jun-Wen Zheng ◽  
Jia-Jie Hao ◽  
...  

Aim: This study aimed to develop an effective risk predictor for patients with stage II and III colorectal cancer (CRC). Materials & methods: The prognostic value of p-mTOR (Ser2448) levels was analyzed using Kaplan–Meier survival analysis and Cox regression analysis. Results: The levels of p-mTOR were increased in CRC specimens and significantly correlated with poor prognosis in patients with stage II and III CRC. Notably, the p-mTOR level was an independent poor prognostic factor for disease-free survival and overall survival in stage II CRC. Conclusion: Aberrant mTOR activation was significantly associated with the risk of recurrence or death in patients with stage II and III CRC, thus this activated proteins that may serve as a potential biomarker for high-risk CRC.


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