Evidence map›Paper›PMID 29799846›Full record

ArticlePloS one2018

Comprehensive analysis of T cell leukemia signals reveals heterogeneity in the PI3 kinase-Akt pathway and limitations of PI3 kinase inhibitors as monotherapy.

Olga Ksionda, Marsilius Mues, Anica M Wandler, Lisa Donker, Milou Tenhagen, Jesse Jun, Gregory S Ducker, Ksenia Matlawska-Wasowska, Kevin Shannon, Kevan M Shokat and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Connectivity Mapping Using a NovelFrontiers in molecular neuroscience · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
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

11 authors at 3 institutions in 1 country.

Olga KsiondaDepartment of Anatomy, University of California San Francisco, San Francisco, California, United States of America.
Marsilius MuesDepartment of Anatomy, University of California San Francisco, San Francisco, California, United States of America.
Anica M WandlerDepartment of Pediatrics, University of California San Francisco, San Francisco, California, United States of America.
Lisa DonkerDepartment of Anatomy, University of California San Francisco, San Francisco, California, United States of America.
Milou TenhagenDepartment of Anatomy, University of California San Francisco, San Francisco, California, United States of America.
Jesse JunDepartment of Anatomy, University of California San Francisco, San Francisco, California, United States of America.
Gregory S DuckerDepartment of Molecular Pharmacology, Howard Hughes Medical Institute, University of California San Francisco, San Francisco, California, United States of America.
Ksenia Matlawska-WasowskaDepartment of Pediatrics, Division of Hematology-Oncology, University of New Mexico, Health Sciences Center, Albuquerque, New Mexico, United States of America.
Kevin ShannonDepartment of Pediatrics, University of California San Francisco, San Francisco, California, United States of America.
Kevan M ShokatDepartment of Molecular Pharmacology, Howard Hughes Medical Institute, University of California San Francisco, San Francisco, California, United States of America.
Jeroen P RooseDepartment of Anatomy, University of California San Francisco, San Francisco, California, United States of America.ORCID 0000-0003-4746-2811
University of California, San Francisco · USHoward Hughes Medical Institute · USUniversity of New Mexico · US

Funding

The PIP2-virus interface and PI 4-kinase: novel biology and validation targetsR01AI099245 · NIAID · STANFORD UNIVERSITY · PI GLENN, JEFFREY S · 2012 to 2016
$5.2M
Balanced signaling cues to guide cell transitions in the blood lineage continuumR01HL120724 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHAKRABORTY, ARUP K., NOLAN, GARRY P · 2015 to 2019
$3.7M
Molecular understanding of leukemic bone marrow cytokine-Ras signals and metabolic dependenceR01CA187318 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JEROEN ROOSE · 2015 to 2026
$3.6M
NCI NIH HHS R01 CA187318NHLBI NIH HHS R01 HL120724NIAID NIH HHS R01 AI099245NIH HHS R01 - CA187318NIH HHS R01 - HL120724NIH HHS RO1AI099245
6 · The paper itself

Abstract

T cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematologic cancer. Poly-chemotherapy with cytotoxic and genotoxic drugs causes substantial toxicity and more specific therapies targeting the underlying molecular lesions are highly desired. Perturbed Ras signaling is prevalent in T-ALL and occurs via oncogenic RAS mutations or through overexpression of the Ras activator RasGRP1 in ~65% of T-ALL patients. Effective small molecule inhibitors for either target do not currently exist. Genetic and biochemical evidence link phosphoinositide 3-kinase (PI3K) signals to T-ALL, PI3Ks are activated by Ras-dependent and Ras-independent mechanisms, and potent PI3K inhibitors exist. Here we performed comprehensive analyses of PI3K-Akt signaling in T-ALL with a focus on class I PI3K. We developed a multiplex, multiparameter flow cytometry platform with pan- and isoform-specific PI3K inhibitors. We find that pan-PI3K and PI3K γ-specific inhibitors effectively block basal and cytokine-induced PI3K-Akt signals. Despite such inhibition, GDC0941 (pan-PI3K) or AS-605240 (PI3Kγ-specific) as single agents did not efficiently induce death in T-ALL cell lines. Combination of GDC0941 with AS-605240, maximally targeting all p110 isoforms, exhibited potent synergistic activity for clonal T-ALL lines in vitro, which motivated us to perform preclinical trials in mice. In contrast to clonal T-ALL lines, we used a T-ALL cancer model that recapitulates the multi-step pathogenesis and inter- and intra-tumoral genetic heterogeneity, a hallmark of advanced human cancers. We found that the combination of GDC0941 with AS-605240 fails in such trials. Our results reveal that PI3K inhibitors are a promising avenue for molecular therapy in T-ALL, but predict the requirement for methods that can resolve biochemical signals in heterogeneous cell populations so that combination therapy can be designed in a rational manner.

Indexed as

Phosphoinositide-3 Kinase InhibitorsAnimalsApoptosisCell ProliferationGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticHumansIndazolesMiceMice, Inbred C57BLPhosphatidylinositol 3-KinasesPrecursor T-Cell Lymphoblastic Leukemia-LymphomaProtein Kinase InhibitorsProto-Oncogene Proteins c-aktSignal TransductionSulfonamides2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3,2-d)pyrimidineIndazolesPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsProtein Kinase InhibitorsProto-Oncogene Proteins c-aktSulfonamides

Identifiers

PMID29799846
PMCPMC5969748
OpenAlexW2803982410

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.