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Cited by 420

The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.

Cancer-specific mutations in PIK3CA are oncogenic in vivo

Open access
Bader, Andreas G., Kang, Sohye, Vogt, Peter K.·2006·Proceedings of the National Academy of Sciences

Abstract

The PIK3CA gene, coding for the catalytic subunit p110α of class IA phosphatidylinositol 3-kinases (PI3Ks), is frequently mutated in human cancer. Mutated p110α proteins show a gain of enzymatic function in vitro and are oncogenic in cell culture. Here, we show that three prevalent mutants of p110α, E542K, E545K, and H1047R, are oncogenic in vivo . They induce tumors in the chorioallantoic membrane of the chicken embryo and cause hemangiosarcomas in the animal. These tumors are marked by increased angiogenesis and an activation of the Akt pathway. The target of rapamycin inhibitor RAD001 blocks tumor growth induced by the H1047R p110α mutant. The in vivo oncogenicity of PIK3CA mutants in an avian species strongly suggests a critical role for these mutated proteins in human malignancies.

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Metadata

Authors
Bader, A. G., Kang, S., & Vogt, P. K.
Venue
Proceedings of the National Academy of Sciences
Published
2006-01-23
Volume
103
Issue
5
Pages
1475-1479
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2167010784
Cited by
420
References
33
FWCI
12.16
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Cancer-specific mutations in PIK3CA are oncogenic in vivo. https://app.cochat.ai/papers/10.1073/pnas.0510857103
The paper
Bader, A. G., Kang, S., & Vogt, P. K. (2006). Cancer-specific mutations in PIK3CA are oncogenic in vivo. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.0510857103

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.