Evidence map›Paper›PMID 29805773›Full record

ReviewOncotarget2018

Stromal cells in breast cancer as a potential therapeutic target.

Samantha S Dykes, Veronica S Hughes, Jennifer M Wiggins, Henrietta O Fasanya, Mai Tanaka, Dietmar Siemann

Abstract readReview
In one paragraph

Review in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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  16. Immunotherapy: breaching the barriers for cancer treatment.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Review
  17. Article
  18. Article
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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

6 authors.

Samantha S DykesDepartment of Radiation Oncology, University of Florida, Gainesville, Florida, USA.
Veronica S HughesDepartment of Radiation Oncology, University of Florida, Gainesville, Florida, USA.
Jennifer M WigginsDepartment of Radiation Oncology, University of Florida, Gainesville, Florida, USA.
Henrietta O FasanyaDepartment of Radiation Oncology, University of Florida, Gainesville, Florida, USA.
Mai TanakaDepartment of Radiation Oncology, University of Florida, Gainesville, Florida, USA.
Dietmar SiemannDepartment of Radiation Oncology, University of Florida, Gainesville, Florida, USA.

Funding

Together: Transforming and Translating Discovery to Improve HealthTL1TR001428 · NCATS · UNIVERSITY OF FLORIDA · PI MCCORMACK, WAYNE T. · 2015 to 2023
$3.9M
Hypoxia: Impact on Src Signaling and Prostate CancerR01CA197477 · NCI · UNIVERSITY OF FLORIDA · PI SIEMANN, DIETMAR W · 2016 to 2020
$1.7M
Targeting Cathepsin L: A Novel Strategy to Impede Prostate and Breast Cancer MetaR01CA169300 · NCI · UNIVERSITY OF FLORIDA · PI SIEMANN, DIETMAR W · 2013 to 2017
$1.5M
NCATS NIH HHS TL1 TR001428NCI NIH HHS R01 CA169300NCI NIH HHS R01 CA197477
6 · The paper itself

Abstract

Breast cancer in the United States is the second most commonly diagnosed cancer in women. About 1 in 8 women will develop invasive breast cancer over the course of her lifetime and breast cancer remains the second leading cause of cancer-related death. In pursuit of novel therapeutic strategies, researchers have examined the tumor microenvironment as a potential anti-cancer target. In addition to neoplastic cells, the tumor microenvironment is composed of several critical normal cell types, including fibroblasts, vascular and lymph endothelial cells, osteoclasts, adipocytes, and immune cells. These cells have important roles in healthy tissue stasis, which frequently are altered in tumors. Indeed, tumor-associated stromal cells often contribute to tumorigenesis, tumor progression, and metastasis. Consequently, these host cells may serve as a possible target in anti-tumor and anti-metastatic therapeutic strategies. Targeting the tumor associated host cells offers the benefit that such cells do not mutate and develop resistance in response to treatment, a major cause of failure in cancer therapeutics targeting neoplastic cells. This review discusses the role of host cells in the tumor microenvironment during tumorigenesis, progression, and metastasis, and provides an overview of recent developments in targeting these cell populations to enhance cancer therapy efficacy.

Indexed as

breast cancermicroenvironmentstromal cells

Identifiers

PMID29805773
PMCPMC5955086

What OpenQuestion holds

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Registered trials

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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.