Genetic alterations of lung cancer (WP1968)
Rattus norvegicus
Expression patterns of two major tumor suppressor pathways in lung cancer. These pathways are functionally linked to lung cancer and play role as a component of checkpoints and growth inhibitory pathways. Components which/who are activated in this pathway are Egfr, Erbb2, Rasl11b, and MYC in the Oncogenic singalling part. Frequent inactivated are TGF-beta R1/2, RB, p16INK4A, Tp53, and p14ARF, whie infrequent inactivated are Smad2 and Sma4. Both, the p14ARF/p53 and the p16INK4A/RB pathway lead to cell cycle arrest.
Authors
Gustav , Kristina Hanspers , Martina Summer-Kutmon , Christine Chichester , Jonathan Mélius , Alex Pico , Egon Willighagen , Friederike Ehrhart , Lauren J. Dupuis , and Marvin MartensActivity
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Organisms
Rattus norvegicusCommunities
Annotations
Pathway Ontology
cancer pathway lung cancer pathwayDisease Ontology
lung cancerReferences
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- Repression of p15INK4b expression by Myc through association with Miz-1. Staller P, Peukert K, Kiermaier A, Seoane J, Lukas J, Karsunky H, et al. Nat Cell Biol. 2001 Apr;3(4):392–9. PubMed Europe PMC Scholia
- HER-2/neu induces p53 ubiquitination via Akt-mediated MDM2 phosphorylation. Zhou BP, Liao Y, Xia W, Zou Y, Spohn B, Hung MC. Nat Cell Biol. 2001 Nov;3(11):973–82. PubMed Europe PMC Scholia
- Genetic alterations of multiple tumor suppressors and oncogenes in the carcinogenesis and progression of lung cancer. Osada H, Takahashi T. Oncogene. 2002 Oct 21;21(48):7421–34. PubMed Europe PMC Scholia