Evidence map›Paper›PMID 29430386›Full record

ArticleCurrent molecular biology reports2017

Tumor microenvironment heterogeneity: challenges and opportunities.

F Runa, S Hamalian, K Meade, P Shisgal, P C Gray, J A Kelber

Abstract read
In one paragraph

Article in Current molecular biology reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers.

0numbers the graph read from it
0cells of the map it votes in
106citing 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

106 citing papers in PubMed.

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  16. Targeting cuproptosis in liver cancer: Molecular mechanisms and therapeutic implications.Apoptosis : an international journal on programmed cell death · 2025
    Review
  17. Article
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  20. Article

46 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

6 authors.

F RunaDepartment of Biology, California State University, Northridge, CA.
S HamalianDepartment of Biology, California State University, Northridge, CA.
K MeadeDepartment of Biology, California State University, Northridge, CA.
P ShisgalDepartment of Biology, California State University, Northridge, CA.
P C GrayThe Salk Institute for Biological Studies, La Jolla, CA.
J A KelberDepartment of Biology, California State University, Northridge, CA.

Funding

SPATIOTEMPORAL MECHANISMS OF EIF5A1/2-MEDIATED METASTASIS IN TRIPLE-NEGATIVE BREAST CANCERSC1GM121182 · NIGMS · CALIFORNIA STATE UNIVERSITY NORTHRIDGE · PI KELBER, JONATHAN · 2017 to 2024
$3.2M
NIGMS NIH HHS SC1 GM121182
6 · The paper itself

Abstract

The tumor microenvironment (TME) has been recognized as an integral component of malignancies in breast and prostate tissues, contributing in confounding ways to tumor progression, metastasis, therapy resistance and disease recurrence. Major components of the TME are immune cells, fibroblasts, pericytes, endothelial cells, mesenchymal stroma/stem cells (MSCs), and extracellular matrix (ECM) components. Herein, we discuss the molecular and cellular heterogeneity within the TME and how this presents unique challenges and opportunities for treating breast and prostate cancers.

Indexed as

Cancer Associated FibroblastsCancer Progression/RecurrenceEMTExtracellular matrix (ECM)Mesenchymal Stem Cells (MSCs)MetastasisSignaling PathwaysTherapy ResistancesTumor Associated Macrophages (TAMs)Tumor Microenvironment (TME)

Identifiers

PMID29430386
PMCPMC5802345

What OpenQuestion holds

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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.