دورية أكاديمية

The Activation Status of the TGF-β Transducer Smad2 Is Associated with a Reduced Survival in Gastrointestinal Cancers: A Systematic Review and Meta-Analysis.

التفاصيل البيبلوغرافية
العنوان: The Activation Status of the TGF-β Transducer Smad2 Is Associated with a Reduced Survival in Gastrointestinal Cancers: A Systematic Review and Meta-Analysis.
المؤلفون: Girolami, Ilaria1 (AUTHOR), Veronese, Nicola2 (AUTHOR), Smith, Lee3 (AUTHOR), Caruso, Maria G.2 (AUTHOR), Reddavide, Rosa2 (AUTHOR), Leandro, Gioacchino2 (AUTHOR), Demurtas, Jacopo4 (AUTHOR), Nottegar, Alessia5 (AUTHOR) alessia.nottegar@gmail.com
المصدر: International Journal of Molecular Sciences. Aug2019, Vol. 20 Issue 15, p3831-3831. 1p. 1 Diagram, 3 Charts.
مصطلحات موضوعية: *TRANSFORMING growth factors-beta, *GASTROINTESTINAL cancer, *META-analysis, *CANCER-related mortality, *TRANSDUCERS, *TRANSFORMING growth factors
مستخلص: Aberrant function of Smad2, a crucial member of transforming growth factor beta (TGF-β) signaling, is associated with the development of malignancies, particularly in the gastrointestinal district. However, little is known about its possible prognostic role in such tumor types. With the first meta-analysis on this topic, we demonstrated that the lack of the activated form of Smad2 (phosphor-Smad2 or pSmad2), which was meant to be the C-terminally phosphorylated form, showed a statistically significant association with an increased risk of all-cause mortality in patients with gastrointestinal cancers (RR, 1.58; 95% CI, 1.05–2.37, p = 0.029, I2 = 84%), also after having adjusted for potential confounders (RR, 1.65; 95% CI, 1.24–2.18; p < 0.001; I2 = 4%). This finding highlights the importance of the TGF-β signaling in this type of cancer. In this line, further studies are needed to explore more in depth this important molecular pathway, focusing also on potential therapeutic strategies based on its effectors or molecular targets. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:16616596
DOI:10.3390/ijms20153831