scholarly journals Prognostic Role of c-Jun Activation in Patients with Areca Quid Chewing-related Oral Squamous Cell Carcinomas in Taiwan

2006 ◽  
Vol 105 (3) ◽  
pp. 229-234 ◽  
Author(s):  
Ru-Cheng Kuo ◽  
Chiao-Ying Lin ◽  
Mark Yen-Ping Kuo
2019 ◽  
pp. 014556131989386
Author(s):  
Serdar Tokmak ◽  
Deniz Arık ◽  
Özgür Pınarbaşlı ◽  
Melek Kezban Gürbüz ◽  
Mustafa Fuat Açıkalın

Introduction: In squamous cell carcinomas of the oral cavity, factors that can predict prognosis are being studied. However, new prognostic factors are needed to provide information on the biological properties of tumors. Galectin-3 is known to be involved in many biological events such as cell adhesion and differentiation, angiogenesis, apoptosis, tumorigenesis, and metastasis. In our study, the prognostic role of galectin-3 expression in squamous cell carcinomas of the oral cavity was investigated. Materials and Methods: The study included 60 patients with a diagnosis of squamous cell carcinoma of the oral cavity. The demographic characteristics of the patients were compiled from the patient files. Galectin-3 expression was studied immunohistochemically. Cytoplasmic and nuclear expressions of galectin-3 were evaluated separately. In addition, the total expression score was calculated by multiplying the percentage and intensity scores for each cases. The critical expression score was determined according to the median value of the total scores. Results: Among 60 cases, 28 tumors were located on the lip, 21 on the tongue, 4 on the floor of the mouth, 3 on the orobuccal mucosa, 3 on the retromolar trigone, and 1 on the gingivobuccal junction. There was no statistically significant relationship between prognosis and nuclear or cytoplasmic galectin-3 expression. Tumor grade and invasion pattern were found to be associated with the galectin-3 total expression score. Conclusion: Although galectin-3 total expression score was correlated with the tumor grade and invasion pattern, it is not associated with overall survival or recurrence rates. However, there is a need for a large series of cases in which methods are standardized in order to clarify the prognostic role of galectin-3 expression in oral squamous cell carcinomas.


1996 ◽  
Vol 110 (3) ◽  
pp. 237-239 ◽  
Author(s):  
S. K. Sarker ◽  
P. Tierney ◽  
K. S. Patel ◽  
C. Fisher ◽  
D. V. Coleman

AbstractPloidy status of squamous cell carcinomas of the head and neck (SCCHN) from primary and recurrent tonsillar and tongue lesions has not been compared using image cytometry. We have measured and compared the DNA indices in 41 cases. There were 29 tongue SCCHN, 20/29 were primary and 9/29 were recurrent. Mean DNA index (DI) was 1.19 (range 0.70–1.81) and 1.28 (range 0.79–1.94) respectively. There were 12 tonsillar cases, 10/12 primary and two out of 12 recurrent. Mean DI was 0.84 (range 0.57–1.09) and 1.00 (range 0.98–1.02) respectively. Mean DNA indices of both primary carcinomas were lower than the mean DNA indices of the recurrent carcinomas. This difference between the two groups may be a reflection of their tumour biology. However, since our study is small no definite conclusions can be made at this stage. We aim in the future to evaluate the prognostic role of DNA indices of patients with paired primary and recurrent SCCHN. This may be of clinical value and improve the treatment modalities available to this group.


2013 ◽  
Vol 20 (1) ◽  
pp. 99-106 ◽  
Author(s):  
Györgyi A. Nelhűbel ◽  
Boróka Károly ◽  
Balázs Szabó ◽  
Gábor Lotz ◽  
András Kiss ◽  
...  

2004 ◽  
Vol 165 (6) ◽  
pp. 2147-2155 ◽  
Author(s):  
Shojiro Kitajima ◽  
Yasusei Kudo ◽  
Ikuko Ogawa ◽  
Tarig Bashir ◽  
Masae Kitagawa ◽  
...  

2011 ◽  
Vol 58 (2) ◽  
pp. 67-74
Author(s):  
Nikola Tanic ◽  
Nasta Dedovic-Tanic ◽  
Brandon Popovic ◽  
Rade Kosanovic ◽  
Jelena Milasin

Oral squamous cell carcinomas (OSCCs) are associated with poor prognosis, and despite advances in therapy approaches, no major improvement in survival has been achieved in the recent years. Efforts are now directed toward finding new biological markers that could predict tumor behavior more accurately. OSCCs, as the majority of malignant tumors, arise from progressive accumulation of genetic and epigenetic lesions, transforming normal cells into malignant. In this paper, an analysis of current studies directed to understanding the underlying mechanisms of OSCC pathogenesis was presented. The emphasis was put on mutational analysis of cancer genes, as well as on the role of viral infections and methylation processes in OSCC. Finally, an overview of studies that tried to determine the possibility for developing OSCC was given.


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