Evidence map›Paper›PMID 33726836›Full record

ArticleCell & bioscience2021

EGFL6 promotes colorectal cancer cell growth and mobility and the anti-cancer property of anti-EGFL6 antibody.

Ting-Yi Sung, Han-Li Huang, Chun-Chun Cheng, Fu-Ling Chang, Po-Li Wei, Ya-Wen Cheng, Cheng-Chiao Huang, Yu-Ching Lee, Wei-Chun HuangFu, Shiow-Lin Pan

Open access · goldAbstract read
In one paragraph

Article in Cell & bioscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-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

10 citing papers in PubMed, 19 citations in OpenAlex.

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  10. Progress of EGFL6 in angiogenesis and tumor development.International journal of clinical and experimental pathology · 2022
    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

10 authors at 2 institutions in 1 country.

Ting-Yi Sung *Ph.D. Program in Drug Discovery and Development Industry, College of Pharmacy, Taipei Medical University, 11031, Taipei, Taiwan.
Han-Li Huang *Ph.D. Program in Drug Discovery and Development Industry, College of Pharmacy, Taipei Medical University, 11031, Taipei, Taiwan.
Chun-Chun ChengGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, No. 250, Wuxing St., 11031, Taipei, Taiwan.
Fu-Ling ChangGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, No. 250, Wuxing St., 11031, Taipei, Taiwan.
Po-Li WeiGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, No. 250, Wuxing St., 11031, Taipei, Taiwan.
Ya-Wen ChengPh.D. Program for Cancer Molecular Biology and Drug Discovery, Taipei Medical University, Taipei, Taiwan.
Cheng-Chiao HuangGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, No. 250, Wuxing St., 11031, Taipei, Taiwan. GS4912@gmail.com.
Yu-Ching LeePh.D. Program in Drug Discovery and Development Industry, College of Pharmacy, Taipei Medical University, 11031, Taipei, Taiwan. ycl@tmu.edu.tw.
Wei-Chun HuangFuPh.D. Program in Drug Discovery and Development Industry, College of Pharmacy, Taipei Medical University, 11031, Taipei, Taiwan. clarehf@tmu.edu.tw.
Shiow-Lin PanPh.D. Program in Drug Discovery and Development Industry, College of Pharmacy, Taipei Medical University, 11031, Taipei, Taiwan. slpan@tmu.edu.tw.ORCID http://orcid.org/0000-0001-7449-3539
Taipei Medical University · TWTaipei Medical University Hospital · TW

Funding

Taipei Medical University Hospital 106TMU-TMUH-10
6 · The paper itself

Abstract

backgroundThe availability of a reliable tumor target for advanced colorectal cancer (CRC) therapeutic approaches is critical since current treatments are limited. Epidermal growth factor-like domain 6 (EGFL6) has been reported to be associated with cancer development. Here, we focused on the role of EGFL6 in CRC progression and its clinical relevance. In addition, an anti-EGFL6 antibody was generated by phage display technology to investigate its potential therapeutic efficacy in CRC.

resultsEGFL6 expression significantly increased in the colon tissues from CRC patients and mice showing spontaneous tumorigenesis, but not in normal tissue. Under hypoxic condition, EGFL6 expression was enhanced at both protein and transcript levels. Moreover, EGFL6 could promote cancer cell migration invasion, and proliferation of CRC cells via up-regulation of the ERK/ AKT pathway. EGFL6 also regulated cell migration, invasion, proliferation, and self-renewal through EGFR/αvβ3 integrin receptors. Treatment with the anti-EGFL6 antibody EGFL6-E5-IgG showed tumor-inhibition and anti-metastasis abilities in the xenograft and syngeneic mouse models, respectively. Moreover, EGFL6-E5-IgG treatment had no adverse effect on angiogenesis and wound healing

conclusionsWe demonstrated that EGFL6 plays a role in CRC tumorigenesis and tumor progression, indicating that EGFL6 is a potential therapeutic target worth further investigation.

Indexed as

Colorectal cancerEGFL6EGFR/αvβ3Therapeutic antibodyTumor progression

Identifiers

PMID33726836
PMCPMC7962215
OpenAlexW3101757643

What Socratic holds

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LicenceCC BY
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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 Socratic graph.