Evidence map›Paper›PMID 28609652›Full record

ArticleCancer cell2017

Paradoxical Effects of MLL Paralogs in MLL-Rearranged Leukemia.

Michael J Thirman

Open access · bronzeAbstract readComment
In one paragraph

Article in Cancer cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Michael J ThirmanSection of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL 60637, USA. Electronic address: mthirman@medicine.bsd.uchicago.edu.
University of Chicago · US

Funding

Instructive role of MLL fusion proteins in lineage determination and leukemogenesisR01CA215504 · NCI · UNIVERSITY OF CHICAGO · PI MULLOY, JAMES C, THIRMAN, MICHAEL J · 2017 to 2021
$3.0M
Genomic prediction tools developed using phenotypes from disease progression modelsK23GM112128 · NIGMS · UNIVERSITY OF CHICAGO · PI SHARMA, MANISH · 2015 to 2018
$764k
NCI NIH HHS R01 CA215504NIGMS NIH HHS K23 GM112128
6 · The paper itself

Abstract

Conflicting data exist on the requirement for wild-type MLL1 in MLL-rearranged leukemia. In this issue of Cancer Cell, Chen et al. describe complementary approaches demonstrating that MLL1 is dispensable for MLL-fusion-mediated leukemogenesis. They also observe an unexpected role for MLL2 in MLL-rearranged leukemia cells and identify potential therapeutic targets.

Indexed as

LeukemiaMyeloid-Lymphoid Leukemia ProteinHistone-Lysine N-MethyltransferaseHumansHistone-Lysine N-MethyltransferaseMyeloid-Lymphoid Leukemia Protein

Identifiers

PMID28609652
PMCPMC5783294
OpenAlexW2624155138

What OpenQuestion holds

Textmetadata
LicenceTDM
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.