Evidence map›Paper›PMID 24857921›Full record

ReviewInternational journal of molecular sciences2014

Brain metastasis-initiating cells: survival of the fittest.

Mohini Singh, Branavan Manoranjan, Sujeivan Mahendram, Nicole McFarlane, Chitra Venugopal, Sheila K Singh

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2014. 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.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Cancer Cell Dormancy in Metastasis.Cold Spring Harbor perspectives in medicine · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. 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

6 authors.

Mohini SinghMcMaster Stem Cell and Cancer Research Institute, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4K1, Canada. msingh0285@hotmail.com.
Branavan ManoranjanMcMaster Stem Cell and Cancer Research Institute, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4K1, Canada. branavan.manoranjan@medportal.ca.
Sujeivan MahendramMcMaster Stem Cell and Cancer Research Institute, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4K1, Canada. smahendram@gmail.com.
Nicole McFarlaneMcMaster Stem Cell and Cancer Research Institute, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4K1, Canada. mcfarln@mcmaster.ca.
Chitra VenugopalMcMaster Stem Cell and Cancer Research Institute, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4K1, Canada. venugop@mcmaster.ca.
Sheila K SinghMcMaster Stem Cell and Cancer Research Institute, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4K1, Canada. ssingh@mcmaster.ca.

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Brain metastases (BMs) are the most common brain tumor in adults, developing in about 10% of adult cancer patients. It is not the incidence of BM that is alarming, but the poor patient prognosis. Even with aggressive treatments, median patient survival is only months. Despite the high rate of BM-associated mortality, very little research is conducted in this area. Lack of research and staggeringly low patient survival is indicative that a novel approach to BMs and their treatment is needed. The ability of a small subset of primary tumor cells to produce macrometastases is reminiscent of brain tumor-initiating cells (BTICs) or cancer stem cells (CSCs) hypothesized to form primary brain tumors. BTICs are considered stem cell-like due to their self-renewal and differentiation properties. Similar to the subset of cells forming metastases, BTICs are most often a rare subpopulation. Based on the functional definition of a TIC, cells capable of forming a BM could be considered to be brain metastasis-initiating cells (BMICs). These putative BMICs would not only have the ability to initiate tumor growth in a secondary niche, but also the machinery to escape the primary tumor, migrate through the circulation, and invade the neural niche.

Indexed as

AnimalsBlood-Brain BarrierBrain NeoplasmsBreast NeoplasmsFemaleHumansLung NeoplasmsNeoplasm InvasivenessNeoplastic Cells, CirculatingNeoplastic Stem CellsSkin Neoplasms

Identifiers

PMID24857921
PMCPMC4057778

What OpenQuestion holds

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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.