Evidence map›Paper›PMID 29293549›Full record

ArticlePloS one2018

Macrophage conditioned medium promotes colorectal cancer stem cell phenotype via the hedgehog signaling pathway.

Fan Fan, Rui Wang, Delphine R Boulbes, Huiyuan Zhang, Stephanie S Watowich, Ling Xia, Xiangcang Ye, Rajat Bhattacharya, Lee M Ellis

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

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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 at 1 institution in 1 country.

Fan FanDepartment of Surgical Oncology, University of Texas MD Anderson Cancer Center, Holcombe Boulevard, Houston, Texas, United States of America.ORCID 0000-0001-6708-5430
Rui WangDepartment of Surgical Oncology, University of Texas MD Anderson Cancer Center, Holcombe Boulevard, Houston, Texas, United States of America.
Delphine R BoulbesDepartment of Surgical Oncology, University of Texas MD Anderson Cancer Center, Holcombe Boulevard, Houston, Texas, United States of America.
Huiyuan ZhangDepartment of Immunology, University of Texas MD Anderson Cancer Center, Holcombe Boulevard, Houston, Texas, United States of America.
Stephanie S WatowichDepartment of Immunology, University of Texas MD Anderson Cancer Center, Holcombe Boulevard, Houston, Texas, United States of America.
Ling XiaDepartment of Surgical Oncology, University of Texas MD Anderson Cancer Center, Holcombe Boulevard, Houston, Texas, United States of America.
Xiangcang YeDepartment of Surgical Oncology, University of Texas MD Anderson Cancer Center, Holcombe Boulevard, Houston, Texas, United States of America.
Rajat BhattacharyaDepartment of Surgical Oncology, University of Texas MD Anderson Cancer Center, Holcombe Boulevard, Houston, Texas, United States of America.
Lee M EllisDepartment of Surgical Oncology, University of Texas MD Anderson Cancer Center, Holcombe Boulevard, Houston, Texas, United States of America.
The University of Texas MD Anderson Cancer Center · US

Funding

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 R01 CA157880NIH HHS CA100879NIH HHS RO1 CA157880
6 · The paper itself

Abstract

backgroundThere is conflicting data on the role of macrophages in colorectal cancer (CRC); some studies have shown that macrophages can exert an anti-tumor effect whereas others show that macrophages are tumor promoting. We sought to determine the role of conditioned medium (CM) from macrophages, in particular classically activated macrophages, on the development of the CSC phenotype in CRC cells, which is believed to mediate tumor growth and chemoresistance.

methodsMurine (CT26) and human (HCP-1) CRC cell lines were treated with CM from lipopolysaccharide (LPS)-activated murine macrophages. The CSC population was assessed using the sphere-forming assay and aldehyde dehydrogenase assay. Chemoresistance studies were performed using the MTT assay. CSC transcription factors and SHH protein were analyzed by Western blotting.

resultsThe results showed that LPS-activated macrophage CM induced the CSC phenotype in CRC cells. Further studies showed that the CSC phenotype was mediated by the sonic hedgehog (SHH)-Gli signaling pathway, which is known to drive self-renewal; these effects were blocked by depletion of SHH in macrophage CM. In addition, LPS-activated macrophage CM enhanced chemoresistance.

conclusionsLPS-activated macrophages play an active role in promoting the CSC phenotype through activation of the SHH-Gli signaling pathway in CRC cells.

Indexed as

AnimalsColorectal NeoplasmsCulture Media, ConditionedHedgehog ProteinsHumansMacrophagesMiceNeoplastic Stem CellsPhenotypeReverse Transcriptase Polymerase Chain ReactionCulture Media, ConditionedHedgehog Proteins

Identifiers

PMID29293549
PMCPMC5749743
OpenAlexW2781976574

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.