Evidence map›Paper›PMID 26497558›Full record

ArticleOncotarget2015

Tumor-host signaling interaction reveals a systemic, age-dependent splenic immune influence on tumor development.

Afshin Beheshti, Justin Wage, J Tyson McDonald, Clare Lamont, Michael Peluso, Philip Hahnfeldt, Lynn Hlatky

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  4. Elucidating Sex-Specific Immune Profiles in a Breast Cancer Model.International journal of molecular sciences · 2024
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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

7 authors at 3 institutions in 1 country.

Afshin BeheshtiDivision of Hematology/Oncology, Molecular Oncology Research Institute, Tufts Medical Center, Boston, MA, USA.
Justin WageCenter of Cancer Systems Biology, Tufts University School of Medicine, Boston, MA, USA.
J Tyson McDonaldCancer Research Center, Hampton University, Hampton, VA, USA.
Clare LamontCenter of Cancer Systems Biology, Tufts University School of Medicine, Boston, MA, USA.
Michael PelusoCenter of Cancer Systems Biology, Tufts University School of Medicine, Boston, MA, USA.
Philip HahnfeldtCenter of Cancer Systems Biology, Tufts University School of Medicine, Boston, MA, USA.
Lynn HlatkyCenter of Cancer Systems Biology, Tufts University School of Medicine, Boston, MA, USA.
Tufts University · USCancer Research Center · USMolecular Oncology (United States) · US

Funding

Project 5 UC BerkleyU54CA149233 · NCI · STEWARD ST. ELIZABETH'S MEDICAL CENTER · PI HLATKY, LYNN · 2010 to 2014
$7.3M
NCI NIH HHS U54 CA149233NCI NIH HHS U54CA149233
6 · The paper itself

Abstract

The concept of age-dependent host control of cancer development raises the natural question of how these effects manifest across the host tissue/organ types with which a tumor interacts, one important component of which is the aging immune system. To investigate this, changes in the spleen, an immune nexus in the mouse, was examined for its age-dependent interactive influence on the carcinogenesis process. The model is the C57BL/6 male mice (adolescent, young adult, middle-aged, and old or 68, 143, 551 and 736 days old respectively) with and without a syngeneic murine tumor implant. Through global transcriptome analysis, immune-related functions were found to be key regulators in the spleen associated with tumor progression as a function of age with CD2, CD3ε, CCL19, and CCL5 being the key molecules involved. Surprisingly, other than CCL5, all key factors and immune-related functions were not active in spleens from non-tumor bearing old mice. Our findings of age-dependent tumor-spleen signaling interaction suggest the existence of a global role of the aging host in carcinogenesis. Suggested is a new avenue for therapeutic improvement that capitalizes on the pervasive role of host aging in dictating the course of this disease.

Indexed as

Age FactorsAnimalsCell ProliferationDisease ProgressionHumansMiceNeoplasmsSignal TransductionSpleenTumor Microenvironmentaging and cancerCD2CD3eGerotargettumor microenvironmenttumor progression

Identifiers

PMID26497558
PMCPMC4742115
OpenAlexW2110875225

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.