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Cited by 593

The DOI matches its Crossref record; 71 of the 71 references it cites were found in a registry or an index.

The PI3K/AKT/mTOR pathway in breast cancer: targets, trials and biomarkers

Open access
Paplomata, Elisavet, O’Regan, Ruth·2014·Therapeutic Advances in Medical Oncology

Abstract

The phosphoinositide 3 kinase (PI3K)/Akt/mammalian (or mechanistic) target of rapamycin (mTOR) pathway is a complicated intracellular pathway, which leads to cell growth and tumor proliferation and plays a significant role in endocrine resistance in breast cancer. Multiple compounds targeting this pathway are being evaluated in clinical trials. These agents are generally well tolerated and can be used in combination with targeted therapies, endocrine therapy or cytotoxic agents. The identification of subtypes of tumors more likely to respond to these therapeutics cannot be overemphasized, since breast cancer is a very heterogeneous malignancy. Activation of pathways such as KRAS and MEK can act as escape mechanisms that lead to resistance, thus a combination of agents targeting multiple steps of the intracellular machinery is promising. There is evidence that tumors with PIK3CA mutations are more sensitive to inhibitors of the PI3K pathway but this has yet to be validated. Large clinical trials with correlative studies are necessary to identify reliable biomarkers of efficacy.

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Metadata

Authors
Paplomata, E., & O’Regan, R.
Venue
Therapeutic Advances in Medical Oncology
Published
2014-04-01
Volume
6
Issue
4
Pages
154-166
ISSN
  • 1758-8340 (ISSN-L)
  • 1758-8359
OpenAlex
W2168133196
Cited by
593
References
71
FWCI
13.14
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: The PI3K/AKT/mTOR pathway in breast cancer: targets, trials and biomarkers. https://app.cochat.ai/papers/10.1177/1758834014530023
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Paplomata, E., & O’Regan, R. (2014). The PI3K/AKT/mTOR pathway in breast cancer: targets, trials and biomarkers. Therapeutic Advances in Medical Oncology. https://doi.org/10.1177/1758834014530023

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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.