Evidence map›Paper›PMID 36189796›Full record

ArticleThe Journal of clinical investigation2022

Harnessing tumorous flaws for immune supremacy: is miRNA-155 the weak link in breast cancer progression?

Samantha Sharma, Mateusz Opyrchal, Xiongbin Lu

Open access · goldAbstract readComment
In one paragraph

Article in The Journal of clinical investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Samantha SharmaDepartment of Medical and Molecular Genetics and.
Mateusz OpyrchalDepartment of Medicine, Division of Hematology/Oncology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Xiongbin LuDepartment of Medical and Molecular Genetics and.
Indiana University Health · US

Funding

Targeting Human Cancers with Hemizygous Deletion of TP53R01CA203737 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LU, XIONGBIN, SCHNEIDER, BRYAN PAUL · 2016 to 2023
$3.4M
Targeting immunoproteasome-mediated antigen presentation in colorectal cancer immunotherapyR01CA260274 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI Mateusz Opyrchal, Xinna Zhang · 2022 to 2026
$2.5M
NCI NIH HHS R01 CA203737NCI NIH HHS R01 CA260274
6 · The paper itself

Abstract

With the advent of immune checkpoint blockade (ICB) therapy, treatment strategies for late-stage cancers have seen a radical advancement. In this issue of the JCI, Wang et al. characterize the functional role of miR-155 in breast cancer and its potential in harnessing the efficacy of immunotherapy. The study reports that high expression levels of miR-155 in breast cancer cells downregulated suppressor of cytokine signaling 1 (SOCS1), increased the phosphorylated STAT1 (pSTAT1)/pSTAT3 ratio, and thereby stimulated chemoattractants for tumor infiltration of effector T cells. Moreover, miR-155 overexpression set the stage for ICB therapy via increased programmed death ligand 1 (PD-L1) expression on cancer cells and enhanced immunological memory response via the release of miR-155-containing extracellular vesicles. Collectively, these data suggest that miR-155 is a strong candidate as a prognostic biomarker for ICB therapy.

Indexed as

Breast NeoplasmsMicroRNAsB7-H1 AntigenBiomarkersChemotactic FactorsCytokinesFemaleHumansImmune Checkpoint InhibitorsImmunotherapyB7-H1 AntigenBiomarkersChemotactic FactorsCytokinesImmune Checkpoint InhibitorsMicroRNAsMIRN155 microRNA, human

Identifiers

PMID36189796
PMCPMC9525109
OpenAlexW4300003835

What OpenQuestion holds

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LicenceCC BY
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.