Literature DB >> 21779503

KRAS Mouse Models: Modeling Cancer Harboring KRAS Mutations.

Rónán C O'Hagan1, Joerg Heyer.   

Abstract

KRAS is a potent oncogene and is mutated in about 30% of all human cancers. However, the biological context of KRAS-dependent oncogenesis is poorly understood. Genetically engineered mouse models of cancer provide invaluable tools to study the oncogenic process, and insights from KRAS-driven models have significantly increased our understanding of the genetic, cellular, and tissue contexts in which KRAS is competent for oncogenesis. Moreover, variation among tumors arising in mouse models can provide insight into the mechanisms underlying response or resistance to therapy in KRAS-dependent cancers. Hence, it is essential that models of KRAS-driven cancers accurately reflect the genetics of human tumors and recapitulate the complex tumor-stromal intercommunication that is manifest in human cancers. Here, we highlight the progress made in modeling KRAS-dependent cancers and the impact that these models have had on our understanding of cancer biology. In particular, the development of models that recapitulate the complex biology of human cancers enables translational insights into mechanisms of therapeutic intervention in KRAS-dependent cancers.

Entities:  

Keywords:  interpatient tumor variation; mouse models harboring KRAS mutation; tumor context; tumor genetics

Year:  2011        PMID: 21779503      PMCID: PMC3128636          DOI: 10.1177/1947601911408080

Source DB:  PubMed          Journal:  Genes Cancer        ISSN: 1947-6019


  106 in total

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Journal:  Cancer Res       Date:  2009-11-10       Impact factor: 12.701

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Journal:  Cell       Date:  2009-05-29       Impact factor: 41.582

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Review 8.  Pharmacogenetics of breast cancer therapies.

Authors:  Daniel L Hertz; Howard L McLeod; Janelle M Hoskins
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Authors:  Ji Luo; Michael J Emanuele; Danan Li; Chad J Creighton; Michael R Schlabach; Thomas F Westbrook; Kwok-Kin Wong; Stephen J Elledge
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Authors:  Sharon Y Gidekel Friedlander; Gerald C Chu; Eric L Snyder; Nomeda Girnius; Gregory Dibelius; Denise Crowley; Eliza Vasile; Ronald A DePinho; Tyler Jacks
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  11 in total

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Authors:  S Andò; R Malivindi; S Catalano; P Rizza; I Barone; S Panza; D Rovito; C Emprou; J-M Bornert; G Laverny; D Metzger
Journal:  Oncogene       Date:  2017-07-24       Impact factor: 9.867

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Journal:  Transgenic Res       Date:  2015-02-26       Impact factor: 2.788

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Authors:  Ruth Nussinov; Chung-Jung Tsai; Hyunbum Jang
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4.  A Genetic Porcine Model of Cancer.

Authors:  Lawrence B Schook; Tiago V Collares; Wenping Hu; Ying Liang; Fernanda M Rodrigues; Laurie A Rund; Kyle M Schachtschneider; Fabiana K Seixas; Kuldeep Singh; Kevin D Wells; Eric M Walters; Randall S Prather; Christopher M Counter
Journal:  PLoS One       Date:  2015-07-01       Impact factor: 3.240

5.  Gedunin inhibits pancreatic cancer by altering sonic hedgehog signaling pathway.

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Review 6.  CRISPR/Cas9: the Jedi against the dark empire of diseases.

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Review 7.  Wnt Signaling Pathways in Keratinocyte Carcinomas.

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8.  Development of thymic tumor in [LSL:KrasG12D; Pdx1-CRE] mice, an adverse effect associated with accelerated pancreatic carcinogenesis.

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9.  Tumor suppressor role of phospholipase C epsilon in Ras-triggered cancers.

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10.  Long-term vemurafenib treatment drives inhibitor resistance through a spontaneous KRAS G12D mutation in a BRAF V600E papillary thyroid carcinoma model.

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