Evidence map›Paper›PMID 28886273›Full record

ArticleCell cycle (Georgetown, Tex.)2017

PARPi potentiates with current conventional therapy in MLL leukemia.

Lu Zhao, Chi Wai Eric So

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Lu Zhaoa Leukemia and Stem Cell Biology Group , Department of Haematological Medicine, King's College London , Denmark Hill campus, London UK.
Chi Wai Eric Soa Leukemia and Stem Cell Biology Group , Department of Haematological Medicine, King's College London , Denmark Hill campus, London UK.
King's College London · GB

Funding

Cancer Research UK 16753
6 · The paper itself

Abstract

Acute myeloid leukemias driven by MLL fusion proteins are commonly associated with poor prognosis and refractory treatment. Here, we provide evidence that olaparib can potentiate sensitivity of MLL leukemia cells to conventional chemotherapy and DNMT inhibitors offering new potential therapeutic strategies for MLL rearranged leukemias Using the primary mouse leukemia cells and human MLL-AF9 leukemic cell line, we demonstrate that treatment of MLL-AF9 leukemic cells with DNMT inhibitors or chemotherapies in combination with olaparib results in significant reduction in colony formation or cell growth while the single agent treatments had little impacts. Combining olaparib with DNMT inhibitor induce cell cycle block and apoptosis. Furthermore, we observe a significant increase in proportion of cells with >10 γH2AX DNA damage foci and double stranded breaks when treated with DNMT inhibitors or chemotherapy agents in combination with olaparib, thus providing possible mechanistic insights for the synergism.

Indexed as

AnimalsCarcinogenesisCell Line, TumorDNA (Cytosine-5-)-MethyltransferasesDNA DamageHistone-Lysine N-MethyltransferaseHumansLeukemiaMiceMyeloid-Lymphoid Leukemia ProteinPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsDNA (Cytosine-5-)-MethyltransferasesHistone-Lysine N-MethyltransferaseKMT2A protein, humanMyeloid-Lymphoid Leukemia ProteinolaparibPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsAMLchemotherapyDNA damageDNMT inhibitorMLLolaparibPARPsynthetic lethality

Identifiers

PMID28886273
PMCPMC5638355
OpenAlexW2750602453

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.