Stable suppression of tumorigenicity by virus-mediated RNA interference.
By T. Brummelkamp, René Bernards, Reuven Agami. Cancer Cell, 2002
1,221 citations recorded by the source corpus.
Subfields: Animal Science and Zoology, Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/55689eec016d1479868b378a9162fa67af0d9fd1
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Citations in the corpus
- Therapeutic EphA2 gene targeting in vivo using neutral liposomal small interfering RNA delivery. (2005, background): “Therefore, most studies using siRNA in vivo involve manipulation of gene expression in a cell line before introduction into an animal model (6, 7) or incorporation of siRNA into a viral vector (8, 9).”
- The BH3 mimetic ABT-737 targets selective Bcl-2 proteins and efficiently induces apoptosis via Bak/Bax if Mcl-1 is neutralized. (2006, methodology): “Retroviral vectors for RNA interference were constructed by ligating annealed oligonucleotides encoding short hairpin sequences into the pRetroSuper vector (Brummelkamp et al., 2002).”
- Inhibition of HIF2α Is Sufficient to Suppress pVHL-Defective Tumor Growth (2003, methodology): “The resulting duplex oligonucleotides were phosphorylated with T4 polynucleotide kinase (Roche Molecular Biochemicals, Mannheim, Germany) according to the manufacturer’s protocol and ligated into pRETRO-SUPER vector (Brummelkamp et al. 2002) cut with BglII and HindIII.”
- Antisense technologies. Improvement through novel chemical modifications. (2003, methodology): “A retroviral vector was used to deliver siRNA that inhibited the carcinogenic K-ras allele in human pancreatic tumor cells [130].”
- The promises and pitfalls of RNA-interference-based therapeutics (2009, neutral): “For example, it was shown that downregulation of an activated Ras oncogene by a lentiviral-delivered shRNA resulted in suppression of tumour growth in mic”
- Suz12 is essential for mouse development and for EZH2 histone methyltransferase activity (2004, methodology): “This sequence works efficiently in both transient transfection as doublestranded RNA and in the retroviral vector pRetroSuper (pRS) (Brummelkamp et al, 2002).”
- Plasminogen activator inhibitor-1 is a critical downstream target of p53 in the induction of replicative senescence (2006, positive): “To investigate the role of PAI-1 in replicative senescence, two independent retroviral vectors were generated that targeted murine PAI-1 for suppression through RNA”
- KRAS: The Critical Driver and Therapeutic Target for Pancreatic Cancer (2018, background): “RNA suppression studies in PDAC cell lines showed the strong requirement for tumorigenic growth (Brummelkamp et al. 2002; Lim and Counter 2005).”
- Senescence impairs successful reprogramming to pluripotent stem cells. (2009, methodology): “, 2004), as well as E6, E7, E6/E7, plasmids; HRAS V12, and plasmid for expression of a shRNA targeting p53 (pRS-shp53) have been described before (Acosta et al., 2008; Brummelkamp et al., 2002).”
- Receptor for RACK1 Mediates Activation of JNK by Protein Kinase C (2005, methodology): “To construct pRS-RACK1, the oligos were annealed and ligated into BglII and HindIII sites of pRetroSuper vector (pRS, Brummelkamp et al., 2002).”
- The KLF4 tumour suppressor is a transcriptional repressor of p53 that acts as a context-dependent oncogene (2005, methodology): “To test this, we used a short hairpin RNA (shRNA) retroviral vector (pRetroSUPER”
- Lentivirus-delivered stable gene silencing by RNAi in primary cells. (2003, methodology): “Lentihair-slLUC and Lentihair-slGFP1 were produced by cotransfection with pHCMVG (Burns et al. 1993) and pCMV R8.”