MicroRNA expression alterations are linked to tumorigenesis and non-neoplastic processes in pancreatic ductal adenocarcinoma
By A. Szafranska, T. Davison, Jeremy J. John, T. Cannon, B. Sipos, A. Maghnouj, E. Labourier, S. Hahn. Oncogene, 2007
698 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/0b021b9818681a02dc2906b9cbbbf683fe6b7f2d
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
- G. Latham
- Danish H Sayed
- Isidore Rigoutsos
- Marcus E. Peter
- Robert Schickel
- Heidi J. Peltier
- Benjamin Boyerinas
- M. Abdellatif
In Molecular Biology
- G. Latham
- Danish H Sayed
- Isidore Rigoutsos
- Marcus E. Peter
- Heidi J. Peltier
- Benjamin Boyerinas
- M. Abdellatif
- Elena Mogilyansky
Citations in the corpus
- miR-155 gene: a typical multifunctional microRNA. (2009, background): “Two independent studies detected a 10-14 fold up regulation of miR-155 in PDAC with respect to normal pancreatic tissue [54, 55].”
- Normalization of microRNA expression levels in quantitative RT-PCR assays: identification of suitable reference RNA targets in normal and cancerous human solid tissues. (2008, background): “Moreover, miRNAs show promise in both diagnostic and therapeutic applications (Wu et al. 2006; Szafranska et al. 2007).”
- MicroRNAs in development and disease. (2011, background): “miR-196a/b’s role was further emphasized as it was strictly detected in cancer tissue and cell lines but not in normal tissue or in pancreatitis (591).”
- MicroRNAs: key players in the immune system, differentiation, tumorigenesis and cell death (2008, background): “overexpressed in pancreatic cancer (Lee et al., 2007; Szafranska et al., 2007).”
- The miR-17/92 cluster: a comprehensive update on its genomics, genetics, functions and increasingly important and numerous roles in health and disease (2013, positive): “In pancreatic cancer, miR-17, miR-18a, miR-19a and miR19b-1 expression levels are increased.(69,70) Another study also showed that the level of miR-18a in the blood is significantly higher before surgery in patients with pancreatic cancer compared with after surgery, suggesting the possibility that ”