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Cited by 355

The DOI matches its Crossref record; 78 of the 78 references it cites were found in a registry or an index.

Targeting the PI3K/Akt/mTOR Pathway - Beyond Rapalogs

Open access
Markman, Ben, Dienstmann, Rodrigo, Tabernero, Josep·2010·Oncotarget

Abstract

It is well established that the PI3K pathway plays a central role in various cellular processes that can contribute to the malignant phenotype. Accordingly, pharmacological inhibition of key nodes in this signaling cascade has been a focus in developmental therapeutics. To date, agents targeting upstream receptor tyrosine kinases are best studied and have achieved greatest clinical success. Further downstream, despite efficacy in certain tumor types, the rapalogs have been somewhat disappointing in the clinic. Novel inhibitors of PI3K, Akt, and mTORC1 and 2 are now passing through early phase clinical trials. It is hoped that these agents will circumvent some of the shortcomings of the rapalogs and lead to meaningful benefits for cancer patients.

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Registry

Crossref · 10.18632/oncotarget.188

Cites

78 of 78 references verified0 citation errors · 0 not checkable

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Metadata

Authors
Markman, B., Dienstmann, R., & Tabernero, J.
Venue
Oncotarget
Published
2010-10-22
Volume
1
Issue
7
Pages
530-543
ISSN
1949-2553 (ISSN-L)
OpenAlex
W2126569401
Cited by
355
References
78
FWCI
11.46
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Targeting the PI3K/Akt/mTOR Pathway - Beyond Rapalogs. https://app.cochat.ai/papers/10.18632/oncotarget.188
The paper
Markman, B., Dienstmann, R., & Tabernero, J. (2010). Targeting the PI3K/Akt/mTOR Pathway - Beyond Rapalogs. Oncotarget. https://doi.org/10.18632/oncotarget.188

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

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.