Evidence map›Paper›PMID 22621920›Full record

ArticleThe Journal of biological chemistry2012

ATP depletion triggers acute myeloid leukemia differentiation through an ATR/Chk1 protein-dependent and p53 protein-independent pathway.

Amitabha Chakrabarti, Kalpana Gupta, James Prabhakar Sharma, Jinbo Yang, Anju Agarwal, Abigail Glick, Youwei Zhang, Munna Agarwal, Mukesh K Agarwal, David N Wald

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. 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
0.4field-weighted citation impact, top 38% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Identification of key pathways and genes inOncoTargets and therapy · 2018
    Article
  7. Article
  8. Article
  9. Purinergic signalling and cancer.Purinergic signalling · 2013
    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

10 authors at 2 institutions in 1 country.

Amitabha ChakrabartiInvenio Therapeutics, Case Western Reserve University, Cleveland, Ohio 44106, USA.
Kalpana Gupta
James Prabhakar Sharma
Jinbo Yang
Anju Agarwal
Abigail Glick
Youwei Zhang
Munna Agarwal
Mukesh K Agarwal
David N Wald
University Hospitals Cleveland Medical Center · USCleveland Clinic · US

Funding

Spatiotemporal Regulation of Chk1 in Cell Biology, Cancer Etiology and TherapyR01CA163214 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI ZHANG, YOU-WEI · 2012 to 2016
$1.6M
Roles of the Checkpoint Kinase Chk1 in Cancer Biology and TherapyR00CA126173 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI ZHANG, YOU-WEI · 2009 to 2011
$740k
NCI NIH HHS R00 CA126173NCI NIH HHS R01 CA163214
6 · The paper itself

Abstract

Despite advances in oncology drug development, most commonly used cancer therapeutics exhibit serious adverse effects. Often the toxicities of chemotherapeutics are due to the induction of significant DNA damage that is necessary for their ability to kill cancer cells. In some clinical situations, the direct induction of significant cytotoxicity is not a requirement to meet clinical goals. For example, differentiation, growth arrest, and/or senescence is a valuable outcome in some cases. In fact, in the case of acute myeloid leukemia (AML), the use of the differentiation agent all-trans-retinoic acid (ATRA) has revolutionized the therapy for a subset of leukemia patients and led to a dramatic survival improvement. Remarkably, this therapeutic approach is possible even in many elderly patients, who would not be able to tolerate therapy with traditional cytotoxic chemotherapy. Because of the success of ATRA, there is widespread interest in identifying differentiation strategies that may be effective for the 90-95% of AML patients who do not clinically respond to ATRA. Utilizing an AML differentiation agent that is in development, we found that AML differentiation can be induced through ATP depletion and the subsequent activation of DNA damage signaling through an ATR/Chk1-dependent and p53-independent pathway. This study not only reveals mechanisms of AML differentiation but also suggests that further investigation is warranted to investigate the potential clinical use of low dose chemotherapeutics to induce differentiation instead of cytotoxicity. This therapeutic approach may be of particular benefit to patients, such as elderly AML patients, who often cannot tolerate traditional AML chemotherapy.

Indexed as

Acute DiseaseAdenosineAdenosine TriphosphateAntibiotics, AntineoplasticAtaxia Telangiectasia Mutated ProteinsBlotting, WesternCaffeineCell Cycle ProteinsCell DifferentiationCell Line, TumorCell ProliferationCheckpoint Kinase 1Comet AssayDNA DamageDoxorubicinHEK293 Cells6-benzylthioinosine7-hydroxystaurosporineAdenosineAdenosine TriphosphateAntibiotics, AntineoplasticAtaxia Telangiectasia Mutated ProteinsATR protein, humanCaffeineCell Cycle ProteinsCheckpoint Kinase 1CHEK1 protein, humanDoxorubicinProtein Kinase InhibitorsProtein KinasesProtein Serine-Threonine KinasesStaurosporineThioinosineTumor Suppressor Protein p53

Identifiers

PMID22621920
PMCPMC3390638
OpenAlexW2018267517

What OpenQuestion holds

Textmetadata
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.