Evidence map›Paper›PMID 26348915›Full record

ArticleNature communications2015

In vivo capture and label-free detection of early metastatic cells.

Samira M Azarin, Ji Yi, Robert M Gower, Brian A Aguado, Megan E Sullivan, Ashley G Goodman, Eric J Jiang, Shreyas S Rao, Yinying Ren, Susan L Tucker and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
8.2field-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

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 163 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. How much do we know about the metastatic process?Clinical & experimental metastasis · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. An engineered niche delineates metastatic potential of breast cancer.Bioengineering & translational medicine · 2024
    Article
  20. Article

15 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

13 authors at 5 institutions in 1 country.

Samira M AzarinDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Ji YiDepartment of Biomedical Engineering, Northwestern University, Evanston, Illinois 60208, USA.
Robert M GowerDepartment of Chemical Engineering, University of South Carolina, Columbia, South Carolina 29208, USA.
Brian A AguadoDepartment of Biomedical Engineering, Northwestern University, Evanston, Illinois 60208, USA.
Megan E SullivanDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, USA.
Ashley G GoodmanDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208, USA.
Eric J JiangDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208, USA.
Shreyas S RaoDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208, USA.
Yinying RenDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208, USA.
Susan L TuckerDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas, 77030, USA.
Vadim BackmanDepartment of Biomedical Engineering, Northwestern University, Evanston, Illinois 60208, USA.
Jacqueline S JerussDepartment of Surgery, University of Michigan, Ann Arbor, Michigan 48105, USA.
Lonnie D SheaDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208, USA.
Northwestern University · USThe University of Texas MD Anderson Cancer Center · USUniversity of Michigan–Ann Arbor · USUniversity of Minnesota · USUniversity of South Carolina · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LEONIDAS C. PLATANIAS · 1993 to 2026
$153.9M
Targeting early ceramide elevation in pre-symptomatic eczemaP20GM103641 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI ENOS, REILLY, NAGARKATTI, PRAKASH S · 2012 to 2023
$20.7M
An in vivo metastasis sensorR01CA173745 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BACKMAN, VADIM, SHEA, LONNIE D · 2012 to 2016
$4.2M
Protein-Releasing Microporous Scaffolds for Cell Replacement TherapyR01EB009910 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUO, XUNRONG, SHEA, LONNIE D · 2010 to 2018
$3.5M
Measuring signaling pathway dynamics during tissue growth in hydrogelsR01GM097220 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JERUSS, JACQUELINE SARA, SHEA, LONNIE D · 2012 to 2015
$1.4M
NCI NIH HHS CA060553NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA173745NCI NIH HHS R01CA173745NIBIB NIH HHS R01 EB009910NIGMS NIH HHS P20 GM103641NIGMS NIH HHS R01 GM097220
6 · The paper itself

Abstract

Breast cancer is a leading cause of death for women, with mortality resulting from metastasis. Metastases are often detected once tumour cells affect the function of solid organs, with a high disease burden limiting effective treatment. Here we report a method for the early detection of metastasis using an implanted scaffold to recruit and capture metastatic cells in vivo, which achieves high cell densities and reduces the tumour burden within solid organs 10-fold. Recruitment is associated with infiltration of immune cells, which include Gr1(hi)CD11b(+) cells. We identify metastatic cells in the scaffold through a label-free detection system using inverse spectroscopic optical coherence tomography, which identifies changes to nanoscale tissue architecture associated with the presence of tumour cells. For patients at risk of recurrence, scaffold implantation following completion of primary therapy has the potential to identify metastatic disease at the earliest stage, enabling initiation of therapy while the disease burden is low.

Indexed as

Biocompatible MaterialsNeoplastic Cells, CirculatingTissue ScaffoldsAdenocarcinomaAnimalsBreast NeoplasmsDisease Models, AnimalEarly Detection of CancerFemaleHumansLiver NeoplasmsLung NeoplasmsMiceNeoplasm MetastasisNeoplasm TransplantationProstheses and ImplantsBiocompatible Materials

Identifiers

PMID26348915
PMCPMC4563812
OpenAlexW1851720544

What OpenQuestion holds

Textmetadata
LicenceTDM
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.