Evidence map›Paper›PMID 26176612›Full record

ArticleCancer biology & therapy2015

Inhibition of class IA PI3K enzymes in non-small cell lung cancer cells uncovers functional compensation among isoforms.

Christopher Stamatkin, Kelley L Ratermann, Colleen W Overley, Esther P Black

Abstract read
In one paragraph

Article in Cancer biology & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Addition of the p110α inhibitor BYL719 overcomes targeted therapy resistance in cells from Her2-positive-PTEN-loss breast cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Christopher Stamatkina University of Kentucky; College of Pharmacy; Department of Pharmaceutical Sciences and Lucille P Markey Cancer Center Lexington ; Lexington , KY USA.
Kelley L Ratermanna University of Kentucky; College of Pharmacy; Department of Pharmaceutical Sciences and Lucille P Markey Cancer Center Lexington ; Lexington , KY USA.
Colleen W Overleya University of Kentucky; College of Pharmacy; Department of Pharmaceutical Sciences and Lucille P Markey Cancer Center Lexington ; Lexington , KY USA.
Esther P Blacka University of Kentucky; College of Pharmacy; Department of Pharmaceutical Sciences and Lucille P Markey Cancer Center Lexington ; Lexington , KY USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deregulation of the phosphatidylinositol 3-kinase (PI3K) pathway is central to many human malignancies while normal cell proliferation requires pathway functionality. Although inhibitors of the PI3K pathway are in clinical trials or approved for therapy, an understanding of the functional activities of pathway members in specific malignancies is needed. In lung cancers, the PI3K pathway is often aberrantly activated by mutation of genes encoding EGFR, KRAS, and PIK3CA proteins. We sought to understand whether class IA PI3K enzymes represent rational therapeutic targets in cells of non-squamous lung cancers by exploring pharmacological and genetic inhibitors of PI3K enzymes in a non-small cell lung cancer (NSCLC) cell line system. We found that class IA PI3K enzymes were expressed in all cell lines tested, but treatment of NSCLC lines with isoform-selective inhibitors (A66, TGX-221, CAL-101 and IC488743) had little effect on cell proliferation or prolonged inhibition of AKT activity. Inhibitory pharmacokinetic and pharmacodynamic responses were observed using these agents at non-isoform selective concentrations and with the pan-class I (ZSTK474) agent. Response to pharmacological inhibition suggested that PI3K isoforms may functionally compensate for one another thus limiting efficacy of single agent treatment. However, combination of ZSTK474 and an EGFR inhibitor (erlotinib) in NSCLC resistant to each single agent reduced cellular proliferation. These studies uncovered unanticipated cellular responses to PI3K isoform inhibition in NSCLC that does not correlate with PI3K mutations, suggesting that patients bearing tumors with wildtype EGFR and KRAS are unlikely to benefit from inhibitors of single isoforms but may respond to pan-isoform inhibition.

Indexed as

Phosphoinositide-3 Kinase InhibitorsAntineoplastic AgentsApoptosisCarcinoma, Non-Small-Cell LungCell Cycle CheckpointsCell Line, TumorCell ProliferationCell SurvivalClass Ia Phosphatidylinositol 3-KinaseDrug Resistance, NeoplasmDrug Screening Assays, AntitumorDrug SynergismErlotinib HydrochlorideGene ExpressionHumansInhibitory Concentration 50Antineoplastic AgentsClass Ia Phosphatidylinositol 3-KinaseErlotinib HydrochlorideidelalisibIsoenzymesMorpholinesPhosphoinositide-3 Kinase InhibitorsPTEN PhosphohydrolasePTEN protein, humanPurinesPyrimidinonesQuinazolinonesTGX 221TriazinesZSTK474PI3K, AKT, mTOR, KRAS, EGFR, drug-resistant, non-squamous

Identifiers

PMID26176612
PMCPMC4622503

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.