Evidence map›Paper›PMID 30669372›Full record

ReviewInternational journal of molecular sciences2019

Targeting PI3K Signaling in Acute Lymphoblastic Leukemia.

Vanessa Edna Sanchez, Cydney Nichols, Hye Na Kim, Eun Ji Gang, Yong-Mi Kim

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 77 citations in OpenAlex.

  1. Review
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  8. Review
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  14. XBP1 promotes NRASJournal of cellular and molecular medicine · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Targeting the lncRNA DUXAP8/miR-29a/Frontiers in oncology · 2022
    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

5 authors at 2 institutions in 1 country.

Vanessa Edna SanchezDepartment of Pathology, Keck School of Medicine of University of Southern California, Los Angeles, CA 90033, USA. vanesses@usc.edu.
Cydney NicholsNew York Medical College School of Medicine, Valhalla, NY 10595, USA. cnichols5@student.nymc.edu.ORCID 0000-0003-4024-5339
Hye Na KimDepartment of Pediatrics, Division of Hematology, Oncology, Blood and Marrow Transplantation, Children's Hospital Los Angeles, University of Southern California, Los Angeles, CA 90027, USA. hyekim@chla.usc.edu.
Eun Ji GangDepartment of Pediatrics, Division of Hematology, Oncology, Blood and Marrow Transplantation, Children's Hospital Los Angeles, University of Southern California, Los Angeles, CA 90027, USA. vanesses@usc.edu.
Yong-Mi KimDepartment of Pediatrics, Division of Hematology, Oncology, Blood and Marrow Transplantation, Children's Hospital Los Angeles, University of Southern California, Los Angeles, CA 90027, USA. ymkim@chla.usc.edu.
University of Southern California · USNew York Medical College · US

Funding

Understanding the niche of minimal residual disease leukemia cellsR01CA172896 · NCI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI KIM, YONG-MI · 2013 to 2022
$3.7M
USC/CHLA Summer Oncology Research Fellowship (SORF) Program for Medical StudentsR25CA225513 · NCI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI ANAT ERDREICH-EPSTEIN, WIJBE MARTIN KAST · 2019 to 2026
$1.7M
NCI NIH HHS R01 CA172896NCI NIH HHS R25 CA225513NIH HHS CA172896
6 · The paper itself

Abstract

Adhesion of acute lymphoblastic leukemia (ALL) cells to bone marrow stroma cells triggers intracellular signals regulating cell-adhesion-mediated drug resistance (CAM-DR). Stromal cell protection of ALL cells has been shown to require active AKT. In chronic lymphocytic leukemia (CLL), adhesion-mediated activation of the PI3K/AKT pathway is reported. A novel FDA-approved PI3Kδ inhibitor, CAL-101/idelalisib, leads to downregulation of p-AKT and increased apoptosis of CLL cells. Recently, two additional PI3K inhibitors have received FDA approval. As the PI3K/AKT pathway is also implicated in adhesion-mediated survival of ALL cells, PI3K inhibitors have been evaluated preclinically in ALL. However, PI3K inhibition has yet to be approved for clinical use in ALL. Here, we review the role of PI3K in normal hematopoietic cells, and in ALL. We focus on summarizing targeting strategies of PI3K in ALL.

Indexed as

Molecular Targeted TherapyAnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsB-LymphocytesClinical Trials as TopicDrug Evaluation, PreclinicalDrug Resistance, NeoplasmHumansIsoenzymesPhosphatidylinositol 3-KinasesPrecursor Cell Lymphoblastic Leukemia-LymphomaProto-Oncogene Proteins c-aktSignal TransductionTreatment OutcomeAntineoplastic AgentsIsoenzymesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktacute lymphoblastic leukemia (ALL)cell adhesion mediated drug resistance (CAM-DR)PI3K/AKTPI3Kδ

Identifiers

PMID30669372
PMCPMC6358886
OpenAlexW2910723008

What Socratic 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 Socratic graph.