Evidence map›Paper›PMID 30894065›Full record

ArticleCancer biology & therapy2019

Cancer-associated fibroblasts promote colorectal cancer progression by secreting CLEC3B.

Hui-Fang Zhu, Xu-Hui Zhang, Chuan-Sha Gu, Yan Zhong, Ting Long, Yi-Dan Ma, Zhi-Yan Hu, Zu-Guo Li, Xiao-Yan Wang

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 61 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 4 institutions in 1 country.

Hui-Fang Zhua Department of Pathology, Nanfang Hospital , Southern Medical University , Guangzhou , Guangdong 510515, China.
Xu-Hui Zhangd Department of Oncology , Guangdong Second Provincial General Hospital , Guangzhou , China.
Chuan-Sha Gua Department of Pathology, Nanfang Hospital , Southern Medical University , Guangzhou , Guangdong 510515, China.
Yan Zhonga Department of Pathology, Nanfang Hospital , Southern Medical University , Guangzhou , Guangdong 510515, China.
Ting Longa Department of Pathology, Nanfang Hospital , Southern Medical University , Guangzhou , Guangdong 510515, China.
Yi-Dan Maa Department of Pathology, Nanfang Hospital , Southern Medical University , Guangzhou , Guangdong 510515, China.
Zhi-Yan Hua Department of Pathology, Nanfang Hospital , Southern Medical University , Guangzhou , Guangdong 510515, China.
Zu-Guo Lia Department of Pathology, Nanfang Hospital , Southern Medical University , Guangzhou , Guangdong 510515, China.
Xiao-Yan Wanga Department of Pathology, Nanfang Hospital , Southern Medical University , Guangzhou , Guangdong 510515, China.
Southern Medical University · CNKey Laboratory of Guangdong Province · CNNanfang Hospital · CNGuangdong Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nontumour cells in the tumour microenvironment, especially fibroblasts, contribute to tumour progression and metastasis. The occurrence and evolution of colorectal cancer (CRC) is closely related to cancer-associated fibroblasts (CAFs). The aim of this work was to evaluate the effects of the growth factors and cytokines secreted by CAFs on CRC progression. The secreted cytokines were examined in CAFs by Human Cytokine Antibody array. We screened 37 differentially secreted cytokines in the culture supernatants of CAFs and NFs. CLEC3B, attractin, kallikrein 5 and legumain were selected for further verification. CLEC3B was more highly expressed in the stroma of CRC tissues than the other 3 cytokines. Immunohistochemistry revealed that CLEC3B expression was associated with serosal invasion by CRC. Patients with co-expression of CLEC3B and α-SMA had worse survival outcomes than those with only CLEC3B or α-SMA expression. CLEC3B secreted from CAFs may promote tumour migration. Knockdown of endogenous CLEC3B in CAFs markedly decreased CRC cell migration, while recombinant human CLEC3B clearly promoted CRC cell migration and actin remodelling. In conclusion, our findings suggest that CAFs promote the CRC cell migration and skeletal reorganization by secreting CLEC3B. CLEC3B might be a potential therapeutic molecule for CRC treatment.

Indexed as

ActinsAdultAgedBiomarkersCancer-Associated FibroblastsCell CycleCell Line, TumorCell ProliferationColorectal NeoplasmsDisease ProgressionFemaleGene Expression ProfilingHumansImmunohistochemistryLectins, C-TypeMaleActinsBiomarkersLectins, C-TypetetranectinCancer-associated fibroblasts (CAFs)CLEC3Bcolorectal cancer (CRC)migrationα-SMA

Identifiers

PMID30894065
PMCPMC6606033
OpenAlexW2922880123

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.