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| Naji, M. |
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| Motta, Antonella |
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| Aletan, Dirar |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Taccardi, Nicola |
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| Kononenko, Denys |
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| Petrov, R. H. | Madrid |
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| Alshaaer, Mazen | Brussels |
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| Bih, L. |
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| Casati, R. |
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| Muller, Hermance |
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| Kočí, Jan | Prague |
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| Šuljagić, Marija |
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| Kalteremidou, Kalliopi-Artemi | Brussels |
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| Azam, Siraj |
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| Ospanova, Alyiya |
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| Blanpain, Bart |
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| Ali, M. A. |
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| Popa, V. |
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| Rančić, M. |
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| Ollier, Nadège |
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| Azevedo, Nuno Monteiro |
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| Landes, Michael |
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| Rignanese, Gian-Marco |
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Pinto, D.
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (9/9 displayed)
- 2023Insertion of MXene-Based Materials into Cu–Pd 3D Aerogels for Electroreduction of CO 2 to Formatecitations
- 2019Fracture characterization of a cast aluminum alloy aiming machining simulationcitations
- 2017The effect of mineralogy, microstructure and firing temperature on the effective thermal conductivity of traditional hot processing ceramicscitations
- 2016Effects of grain size on the reactivity of limestone temper in a kaolinitic claycitations
- 2015Strength of kaolinite-based ceramics: Comparison between limestone- and quartz-tempered bodiescitations
- 2011Transmission electron microscopy investigation of Ag-free lillianite and heyrovskýite from Vulcano, Aeolian Islands, Italycitations
- 2009Tazieffite, Pb20Cd2(As,Bi)22S50Cl10, a new chloro-sulfosalt from Mutnovsky volcano, Kamchatka Peninsula, Russian Federationcitations
- 2006Association of the A870G cyclin D1 gene polymorphism with genetic susceptibility to nasopharyngeal carcinomacitations
- 2003Association between CYP2E1 polymorphisms and susceptibility to prostate cancer
Places of action
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article
Association of the A870G cyclin D1 gene polymorphism with genetic susceptibility to nasopharyngeal carcinoma
Abstract
Background. Nasopharyngeal cancer (NPC) is multifactorial, and the genetic background may be a crucial etiologic factor. Cyclin D1 (CCND1) is a key regulator of the cell cycle, and its altered activity is associated with the development of cancer. Methods. We analyzed the A870G CCND1 polymorphism by polymerase chain reaction/restriction fragment length polymorphism (PCR-RFLP) in 281 individuals, including 94 patients with NPC and 187 healthy individuals. Results. Our results indicate that individuals carrying two G alleles have a 2.17-fold increase in the risk for the development of NPC (odds ratio [OR], 2.17; 95% confidence interval [Cl], 1.19-3.98; p =.016). Age-adjusted logistic regression analysis confirmed this association (adjusted odds ratio [aOR], 2.14; 95% Cl, 1.14-4.04; p =.018). Multivariate analysis demonstrates an independent association between GG CCND1 genotype (aOR, 2.06), male sex (aOR, 2.66), and age at diagnosis (aOR, 2.02) regarding the development of undifferentiated NPC. The proportion of NPC cases attributable to the GG CCND1 genotype was 14,76%. Conclusions. Our results may be important in the definition of a biologic predictive profile for the development of NPC within ourpopulation. (c) 2006 Wiley Periodicals, Inc.