Evidence map›Paper›PMID 27049467›Full record

ReviewCell cycle (Georgetown, Tex.)2016

Aberrant hnRNP K expression: All roads lead to cancer.

Miguel Gallardo, Marisa J Hornbaker, Xiaorui Zhang, Peter Hu, Carlos Bueso-Ramos, Sean M Post

Abstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing 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

59 citing papers in PubMed.

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  15. The SUMOylation and ubiquitination crosstalk in cancer.Journal of cancer research and clinical oncology · 2023
    Review
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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

6 authors.

Miguel Gallardoa Department of Leukemia , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
Marisa J Hornbakera Department of Leukemia , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
Xiaorui Zhanga Department of Leukemia , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
Peter Huc School of Health Professions, The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
Carlos Bueso-Ramosd Department of Hematopathology , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
Sean M Posta Department of Leukemia , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
6 · The paper itself

Abstract

The classification of a gene as an oncogene or a tumor suppressor has been a staple of cancer biology for decades. However, as we delve deeper into the biology of these genes, this simple classification has become increasingly difficult for some. In the case of heterogeneous nuclear ribonuclear protein K (hnRNP K), its role as a tumor suppressor has recently been described in acute myeloid leukemia and demonstrated in a haploinsufficient mouse model. In contrast, data from other clinical correlation studies suggest that hnRNP K may be more fittingly described as an oncogene, due to its increased levels in a variety of malignancies. hnRNP K is a multifunctional protein that can regulate both oncogenic and tumor suppressive pathways through a bevy of chromatin-, DNA-, RNA-, and protein-mediated activates, suggesting its aberrant expression may have broad-reaching cellular impacts. In this review, we highlight our current understanding of hnRNP K, with particular emphasis on its apparently dichotomous roles in tumorigenesis.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCarcinogenesisCCAAT-Enhancer-Binding ProteinsCyclin-Dependent Kinase Inhibitor p21Disease Models, AnimalHaploinsufficiencyHeterogeneous-Nuclear Ribonucleoprotein KHumansLeukemia, Myeloid, AcuteMiceOncogene ProteinsProtein BindingProto-Oncogene Proteins c-mycSignal TransductionTumor Suppressor Protein p53CCAAT-Enhancer-Binding ProteinsCyclin-Dependent Kinase Inhibitor p21Heterogeneous-Nuclear Ribonucleoprotein KOncogene ProteinsProto-Oncogene Proteins c-mycTumor Suppressor Protein p53Tumor Suppressor Proteins9q21.32acute myeloid leukemiaC/EBPc-MychaploinsufficiencyhnRNP Kmouse modelsp21p53

Identifiers

PMID27049467
PMCPMC4934053

What OpenQuestion holds

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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.