Evidence map›Paper›PMID 30302223›Full record

ReviewInternational journal of hematologic oncology2017

Understanding the molecular basis of acute myeloid leukemias: where are we now?

Alicja M Gruszka, Debora Valli, Myriam Alcalay

Abstract readReview
In one paragraph

Review in International journal of hematologic oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. DOGMA-seq and multimodal, single-cell analysis in acute myeloid leukemia.International review of cell and molecular biology · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. JAK-STAT in Early Hematopoiesis and Leukemia.Frontiers in cell and developmental biology · 2021
    Review
  10. RNA Targeting in Acute Myeloid Leukemia.ACS pharmacology & translational science · 2020
    Article
  11. 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

3 authors.

Alicja M GruszkaDepartment of Experimental Oncology, Istituto Europeo di Oncologia, Via Adamello 16, 20139 Milano, Italy.
Debora ValliDepartment of Experimental Oncology, Istituto Europeo di Oncologia, Via Adamello 16, 20139 Milano, Italy.
Myriam AlcalayDepartment of Experimental Oncology, Istituto Europeo di Oncologia, Via Adamello 16, 20139 Milano, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the treatment modalities for acute myeloid leukemia (AML) have not changed much over the past 40 years, distinct progress has been made in deciphering the basic biology underlying the pathogenesis of this group of hematological disorders. Studies show that AML development is a multicause, multistep and multipathway process. Accordingly, AMLs constitute a heterogeneous group of diseases. The thorough understanding of the molecular basis of AML is paving the way for better therapeutic approaches. Multiple novel drugs are being introduced and new, more efficient and less toxic formulations of conventional therapeutics are becoming available. Here, we review the recent advances in the comprehension of the molecular processes that lead to the onset of AML and its translation into clinical practice.

Indexed as

AMLleukemogenesismolecular oncology

Identifiers

PMID30302223
PMCPMC6172002

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.