Evidence map›Paper›PMID 25535733›Full record

ArticleBritish journal of cancer2015

The requirement for freshly isolated human colorectal cancer (CRC) cells in isolating CRC stem cells.

F Fan, S Bellister, J Lu, X Ye, D R Boulbes, F Tozzi, E Sceusi, S Kopetz, F Tian, L Xia and 3 more

Open access · greenAbstract readValidation Study
In one paragraph

Article in British journal of cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 34 citations in OpenAlex.

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  20. Primary cultures of human colon cancer as a model to study cancer stem cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    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

13 authors at 1 institution in 1 country.

F FanDepartment of Surgical Oncology, Unit 1484, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77230-1402, USA.
S BellisterDepartment of Surgical Oncology, Unit 1484, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77230-1402, USA.
J LuDepartment of Surgical Oncology, Unit 1484, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77230-1402, USA.
X YeDepartment of Surgical Oncology, Unit 1484, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77230-1402, USA.
D R BoulbesDepartment of Surgical Oncology, Unit 1484, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77230-1402, USA.
F TozziDepartment of Surgical Oncology, Unit 1484, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77230-1402, USA.
E SceusiDepartment of Surgical Oncology, Unit 1484, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77230-1402, USA.
S KopetzDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
F TianDepartment of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
L XiaDepartment of Surgical Oncology, Unit 1484, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77230-1402, USA.
Y ZhouDepartment of Surgical Oncology, Unit 1484, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77230-1402, USA.
R BhattacharyaDepartment of Surgical Oncology, Unit 1484, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77230-1402, USA.
L M Ellis1] Department of Surgical Oncology, Unit 1484, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77230-1402, USA [2] Department of Molecular and Cellular Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
TRAINING OF ACADEMIC SURGICAL ONCOLOGISTST32CA009599 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Ashley M Holder, Jennifer A. Wargo · 1988 to 2026
$13.2M
Paracrine Role of Endothelial Cells on the Colorectal Cancer Stem Cell PhenotypeR01CA157880 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ELLIS, LEE M. · 2012 to 2016
$1.5M
NCI NIH HHS CA016672NCI NIH HHS CA100879NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA157880NCI NIH HHS R01CA157880NCI NIH HHS T32 CA009599NCI NIH HHS T32CA009599
6 · The paper itself

Abstract

backgroundIsolation of colorectal cancer (CRC) cell populations enriched for cancer stem cells (CSCs) may facilitate target identification. There is no consensus regarding the best methods for isolating CRC stem cells (CRC-SCs). We determined the suitability of various cellular models and various stem cell markers for the isolation of CRC-SCs.

methodsEstablished human CRC cell lines, established CRC cell lines passaged through mice, patient-derived xenograft (PDX)-derived cells, early passage/newly established cell lines, and cells directly from clinical specimens were studied. Cells were FAC-sorted for the CRC-SC markers CD44, CD133, and aldehyde dehydrogenase (ALDH). Sphere formation and in vivo tumorigenicity studies were used to validate CRC-SC enrichment.

resultsNone of the markers studied in established cell lines, grown either in vitro or in vivo, consistently enriched for CRC-SCs. In the three other cellular models, CD44 and CD133 did not reliably enrich for stemness. In contrast, freshly isolated PDX-derived cells or early passage/newly established CRC cell lines with high ALDH activity formed spheres in vitro and enhanced tumorigenicity in vivo, whereas cells with low ALDH activity did not.

conclusionsPDX-derived cells, early passages/newly established CRC cell lines and cells from clinical specimen with high ALDH activity can be used to identify CRC-SC-enriched populations. Established CRC cell lines should not be used to isolate CSCs.

Indexed as

AnimalsCell ProliferationCell SeparationCoculture TechniquesColorectal NeoplasmsHCT116 CellsHT29 CellsHumansHyaluronan ReceptorsMiceMice, NudeNeoplastic Stem CellsPrimary Cell CultureSpheroids, CellularTumor Cells, CulturedHyaluronan Receptors

Identifiers

PMID25535733
PMCPMC4453647
OpenAlexW2044738626

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.