Evidence map›Paper›PMID 26484891›Full record

ArticleJournal of visualized experiments : JoVE2015

Isolation and Propagation of Circulating Tumor Cells from a Mouse Cancer Model.

Dibash K Das, Michelle K Naidoo, Adeodat Ilboudo, Pascal DuBois, Victoria Durojaiye, Chen Liu, Olorunseun O Ogunwobi

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact, top 97% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Biphasic α2β1 Integrin Expression in Breast Cancer Metastasis to Bone.International journal of molecular sciences · 2021
    Article
  4. Article
  5. Article
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

7 authors at 3 institutions in 1 country.

Dibash K DasDepartment of Biological Sciences, Hunter College of The City University of New York; Departments of Biology and Biochemistry, The Graduate Center of The City University of New York.
Michelle K NaidooDepartment of Biological Sciences, Hunter College of The City University of New York.
Adeodat IlboudoDepartment of Biological Sciences, Hunter College of The City University of New York.
Pascal DuBoisDepartment of Biological Sciences, Hunter College of The City University of New York.
Victoria DurojaiyeDepartment of Biological Sciences, Hunter College of The City University of New York.
Chen LiuDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida.
Olorunseun O OgunwobiDepartment of Biological Sciences, Hunter College of The City University of New York; Departments of Biology and Biochemistry, The Graduate Center of The City University of New York; Ogunwobi@genectr.hunter.cuny.edu.
Hunter College · USCity University of New York · USUniversity of Florida · US

Funding

Basic and Translational Research Center for Reducing Health DisparitiesG12MD007599 · NIMHD · HUNTER COLLEGE · PI ANGULO, JESUS A · 2012 to 2017
$14.6M
NIMHD NIH HHS G12 MD007599NIMHD NIH HHS (MD007599
6 · The paper itself

Abstract

Cancer metastasis is the foremost cause of cancer-associated deaths. Recent studies have shown that circulating tumor cells (CTCs) are important in cancer metastasis. Indeed, the number of CTCs correlates with tumor size. Here, a detailed description is provided of a methodology for isolation and propagation of CTCs from a syngeneic mouse model of hepatocellular carcinoma (HCC) which allows for downstream analysis of potentially important molecular mechanisms of solid organ tumor metastasis. This method is efficient and reproducible. It is a non-invasive technique and, therefore, has potential to replace the invasive biopsy of tissues from humans which may be associated with complications. Therefore, the method discussed here allows for the isolation and propagation of CTCs from whole blood samples such that they can be examined and characterized. This has potential for future adaptation for clinical applications such as diagnosis, and personalized targeted therapy.

Indexed as

AnimalsCell SeparationLiver Neoplasms, ExperimentalMiceMice, Inbred BALB CNeoplasm MetastasisNeoplastic Cells, Circulating

Identifiers

PMID26484891
PMCPMC4692643
OpenAlexW1750116901

What OpenQuestion holds

Textmetadata
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.