Evidence map›Paper›PMID 23205268›Full record

ArticleScientific reports2012

Delineation of breast cancer cell hierarchy identifies the subset responsible for dormancy.

Shyam A Patel, Shakti H Ramkissoon, Margarette Bryan, Lillian F Pliner, Gabriela Dontu, Prem S Patel, Sohrab Amiri, Sharon R Pine, Pranela Rameshwar

Abstract read
In one paragraph

Article in Scientific reports, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Tumour Stem Cells in Breast Cancer.International journal of molecular sciences · 2022
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. The Relationship Between Mesenchymal Stem Cells and Tumor Dormancy.Frontiers in cell and developmental biology · 2021
    Review
  15. Review
  16. Exosomes in the Healthy and Malignant Bone Marrow Microenvironment.Advances in experimental medicine and biology · 2021
    Article
  17. Review
  18. Review
  19. Article
  20. Epigenetic dynamics in cancer stem cell dormancy.Cancer metastasis reviews · 2020
    Review
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

9 authors.

Shyam A PatelDepartment of Medicine - Division of Hematology/Oncology, New Jersey Medical School, University of Medicine and Dentistry of New Jersey , Newark, NJ, USA.
Shakti H Ramkissoon
Margarette Bryan
Lillian F Pliner
Gabriela Dontu
Prem S Patel
Sohrab Amiri
Sharon R Pine
Pranela Rameshwar

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI EDMUND C. LATTIME · 1997 to 2026
$94.5M
Asymmetric Cell Division and Notch Signaling in Lung Cancer Stem CellsK22CA140719 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI PINE, SHARON R. · 2011 to 2013
$539k
NCI NIH HHS K22 CA140719NCI NIH HHS P30 CA072720
6 · The paper itself

Abstract

The bone marrow (BM) is a major organ of breast cancer (BC) dormancy and a common source of BC resurgence. Gap junctional intercellular communication (GJIC) between BC cells (BCCs) and BM stroma facilitates dormancy. This study reports on a hierarchy of BCCs with the most immature subset (Oct4(hi)/CD44(hi/med)/CD24(-/+)) demonstrating chemoresistance, dormancy, and stem cell properties: self-renewal, serial passaging ability, cycling quiescence, long doubling time, asymmetric division, high metastatic and invasive capability. In vitro and in vivo studies indicated that this subset was responsible for GJIC with BM stroma. Similar BCCs were detected in the blood of patients despite aggressive treatment and in a patient with a relatively large tumor but no lymph node involvement. In brief, these findings identified a novel BCC subset with stem cell properties, with preference for dormancy and in the circulation of patients. The findings establish a working cellular hierarchy of BCCs based on phenotype and functions.

Indexed as

AnimalsAntineoplastic AgentsBiomarkers, TumorBone Marrow CellsBreast NeoplasmsCarboplatinCD24 AntigenCell CommunicationCell DivisionCell Line, TumorCoculture TechniquesFemaleGap JunctionsHumansHyaluronan ReceptorsMiceAntineoplastic AgentsBiomarkers, TumorCarboplatinCD24 AntigenCD24 protein, humanCD44 protein, humanHyaluronan ReceptorsOctamer Transcription Factor-3POU5F1 protein, human

Identifiers

PMID23205268
PMCPMC3510468

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.