Evidence map›Paper›PMID 22609116›Full record

ArticleThe American journal of pathology2012

Quantitative proteomics reveals that miR-155 regulates the PI3K-AKT pathway in diffuse large B-cell lymphoma.

Xin Huang, Yulei Shen, Miao Liu, Chengfeng Bi, Chunsun Jiang, Javeed Iqbal, Timothy W McKeithan, Wing C Chan, Shi-Jian Ding, Kai Fu

Open access · hybridAbstract read
In one paragraph

Article in The American journal of pathology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 2 pooled it
6.6field-weighted citation impact, top 2% 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

76 citing papers in PubMed, 2 syntheses or guidelines pooled it, 129 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. microRNA-155: a versatile noncoding RNA.Molecular biology reports · 2026
    Review
  7. Review
  8. Article
  9. Cancer-AssociatedInternational journal of medical sciences · 2025
    Review
  10. Review
  11. Review
  12. Article
  13. miR-155: An Important Role in Inflammation Response.Journal of immunology research · 2022
    Review
  14. Review
  15. Dairy consumption and hepatocellular carcinoma risk.Annals of translational medicine · 2021
    Review
  16. Roles of microRNAs in inflammatory bowel disease.International journal of biological sciences · 2021
    Review
  17. Next generation miRNA inhibition using short anti-seed PNAs encapsulated in PLGA nanoparticles.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Article
  18. Article
  19. Article
  20. Review

16 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Xin HuangDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE 68198-3135, USA.
Yulei Shen
Miao Liu
Chengfeng Bi
Chunsun Jiang
Javeed Iqbal
Timothy W McKeithan
Wing C Chan
Shi-Jian Ding
Kai Fu
University of Nebraska Medical Center · US

Funding

Molecular Signatures to Improve Diagnosis and Outcome PrU01CA114778 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI CHAN, WING C. · 2005 to 2009
$8.7M
NCI NIH HHS U01 CA114778NCI NIH HHS U01 CA114778-03
6 · The paper itself

Abstract

The aberrant expression of microRNA-155 (miR-155), which has emerged as having a significant impact on the biological characteristics of lymphocytes, plays important roles in B-cell malignancies, such as diffuse large B-cell lymphoma (DLBCL). DLBCL is the most common non-Hodgkin's lymphoma in the adult population, accounting for approximately 40% of newly diagnosed non-Hodgkin's lymphoma cases globally. To determine the specific function of miR-155, a quantitative proteomics approach was applied to examine the inhibitory effects of miR-155 on protein synthesis in DLBCL cells. PIK3R1 (p85α), a negative regulator of the phosphatidylinositol 3-kinase (PI3K)-AKT pathway, was identified as a direct target of miR-155. A luciferase reporter was repressed through the direct interaction of miR-155 and the p85α 3'-untranslated region, and overexpression of miR-155 down-regulated both the transcription and translation of p85α. The PI3K-AKT signaling pathway was highly activated by the sustained overexpression of miR-155 in DHL16 cells, whereas knockdown of miR-155 in OCI-Ly3 cells diminished AKT activity. Taken together, our results reveal a novel target involved in miR-155 biological characteristics and provide a molecular link between the overexpression of miR-155 and the activation of PI3K-AKT in DLBCL.

Indexed as

3' Untranslated RegionsCell Line, TumorGene Knockdown TechniquesHumansLymphoma, Large B-Cell, DiffuseMicroRNAsPhosphatidylinositol 3-KinaseProteomicsProto-Oncogene Proteins c-aktRNA, NeoplasmSignal TransductionTranscription, Genetic3' Untranslated RegionsMicroRNAsMIRN155 microRNA, humanPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktRNA, Neoplasm

Identifiers

PMID22609116
PMCPMC3388146
OpenAlexW1996787649

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.