Evidence map›Paper›PMID 30470719›Full record

ArticleThe Journal of experimental medicine2018

Bone marrow-derived fibroblasts are a functionally distinct stromal cell population in breast cancer.

Yael Raz, Noam Cohen, Ophir Shani, Rachel E Bell, Sergey V Novitskiy, Lilach Abramovitz, Carmit Levy, Michael Milyavsky, Leonor Leider-Trejo, Harold L Moses and 2 more

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 171 papers.

0numbers the graph read from it
0cells of the map it votes in
171citing papers in PubMed
11.8field-weighted citation impact, top 1% 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

171 citing papers in PubMed, 257 citations in OpenAlex.

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111 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Yael RazDepartment of Pathology, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Noam CohenDepartment of Pathology, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Ophir ShaniDepartment of Pathology, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Rachel E BellDepartment of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Sergey V NovitskiyDepartment of Cancer Biology, Vanderbilt University School of Medicine and Vanderbilt-Ingram Comprehensive Cancer Center, Nashville, TN.
Lilach AbramovitzDepartment of Pathology, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Carmit LevyDepartment of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Michael MilyavskyDepartment of Pathology, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Leonor Leider-TrejoDepartment of Pathology, Tel Aviv Sourasky Medical Center, Tel Aviv University, Tel Aviv, Israel.
Harold L MosesDepartment of Cancer Biology, Vanderbilt University School of Medicine and Vanderbilt-Ingram Comprehensive Cancer Center, Nashville, TN.ORCID 0000-0002-0116-0140
Dan GrisaruDepartment of Obstetrics and Gynecology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Neta ErezDepartment of Pathology, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel netaerez@post.tau.ac.il.ORCID 0000-0001-6506-9074
Tel Aviv University · ILVanderbilt University · USTel Aviv Sourasky Medical Center · IL

Funding

Role of Adenosine in TGF-beta Effects in CancersR01CA200681 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI NOVITSKIY, SERGEY V. · 2016 to 2020
$1.8M
NCI NIH HHS R01 CA200681
6 · The paper itself

Abstract

Cancer-associated fibroblasts (CAFs) are highly prominent in breast tumors, but their functional heterogeneity and origin are still largely unresolved. We report that bone marrow (BM)-derived mesenchymal stromal cells (MSCs) are recruited to primary breast tumors and to lung metastases and differentiate to a distinct subpopulation of CAFs. We show that BM-derived CAFs are functionally important for tumor growth and enhance angiogenesis via up-regulation of Clusterin. Using newly generated transgenic mice and adoptive BM transplantations, we demonstrate that BM-derived fibroblasts are a substantial source of CAFs in the tumor microenvironment. Unlike resident CAFs, BM-derived CAFs do not express PDGFRα, and their recruitment resulted in a decrease in the percentage of PDGFRα-expressing CAFs. Strikingly, decrease in PDGFRα in breast cancer patients was associated with worse prognosis, suggesting that BM-derived CAFs may have deleterious effects on survival. Therefore, PDGFRα expression distinguishes two functionally unique CAF populations in breast tumors and metastases and may have important implications for patient stratification and precision therapeutics.

Indexed as

Tumor MicroenvironmentAnimalsBone Marrow CellsBreast NeoplasmsFemaleFibroblastsHumansMammary Neoplasms, AnimalMesenchymal Stem CellsMiceMice, TransgenicNeoplasm MetastasisNeoplasm ProteinsReceptor, Platelet-Derived Growth Factor alphaNeoplasm ProteinsReceptor, Platelet-Derived Growth Factor alpha

Identifiers

PMID30470719
PMCPMC6279405
OpenAlexW2901741449

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.