Evidence map›Paper›PMID 26840088›Full record

ReviewOncotarget2016

Potential therapeutic implications of IL-6/IL-6R/gp130-targeting agents in breast cancer.

Tae-Hwe Heo, Joseph Wahler, Nanjoo Suh

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
7.2field-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, 117 citations in OpenAlex.

  1. Article
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  4. Review
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  10. Human mutation · 2025
    Article
  11. Review
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  13. Roles of Phytochemicals in Cancer Prevention and Therapeutics.International journal of molecular sciences · 2024
    Article
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  16. Article
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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

3 authors at 2 institutions in 2 countries.

Tae-Hwe HeoNP512, Laboratory of Pharmacoimmunology, Integrated Research Institute of Pharmaceutical Sciences, College of Pharmacy, The Catholic University of Korea, Seoul, Republic of Korea.
Joseph WahlerDepartment of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.
Nanjoo SuhDepartment of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.
Rutgers, The State University of New Jersey · USRutgers Cancer Institute of New Jersey

Funding

Translational Research Support CoreP30ES005022 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI ROBERT John LAUMBACH · 1988 to 2026
$47.4M
Prevention of estrogen-mediated mammary carcinogenesis by mixtures of tocopherolsR01AT007036 · NCCIH · RUTGERS, THE STATE UNIV OF N.J. · PI SUH, NANJOO · 2012 to 2016
$1.9M
Inhibition of breast cancer progression by vitamin D analogs and triterpenoidsR01CA127645 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI SUH, NANJOO · 2008 to 2012
$1.3M
NCCIH NIH HHS R01 AT007036NCI NIH HHS R01 CA127645NIEHS NIH HHS P30 ES005022
6 · The paper itself

Abstract

Interleukin-6 (IL-6) is a pleiotropic cytokine with known multiple functions in immune regulation, inflammation, and oncogenesis. Binding of IL-6 to the IL-6 receptor (IL-6R) induces homodimerization and recruitment of glycoprotein 130 (gp130), which leads to activation of downstream signaling. Emerging evidence suggests that high levels of IL-6 are correlated with poor prognosis in breast cancer patients. IL-6 appears to play a critical role in the growth and metastasis of breast cancer cells, renewal of breast cancer stem cells (BCSCs), and drug resistance of BCSCs, making anti-IL-6/IL-6R/gp130 therapies promising options for the treatment and prevention of breast cancers. However, preclinical and clinical studies of the applications of anti-IL-6/IL-6R/gp130 therapy in breast cancers are limited. In this review, we summarize the structures, preclinical and clinical studies, mechanisms of action of chemical and biological blockers that directly bind to IL-6, IL-6R, or gp130, and the potential clinical applications of these pharmacological agents as breast cancer therapies.

Indexed as

Interleukin-6 InhibitorsAnimalsAntineoplastic AgentsBreast NeoplasmsCytokine Receptor gp130FemaleHumansInterleukin-6Receptors, Interleukin-6Antineoplastic AgentsCytokine Receptor gp130IL6 protein, humanInterleukin-6Interleukin-6 InhibitorsReceptors, Interleukin-6breast cancergp130interleukin-6

Identifiers

PMID26840088
PMCPMC4941253
OpenAlexW2291386925

What OpenQuestion holds

Textmetadata
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.