Evidence map›Paper›PMID 27686285›Full record

ArticleExperimental & molecular medicine2016

CTHRC1 promotes angiogenesis by recruiting Tie2-expressing monocytes to pancreatic tumors.

Jaemin Lee, Jinhoi Song, Eun-Soo Kwon, Seongyea Jo, Min Kyung Kang, Yeon Jeong Kim, Yeonsil Hwang, Hosung Bae, Tae Heung Kang, Suhwan Chang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

28 citing papers in PubMed, 35 citations in OpenAlex.

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  8. Immunosuppressive MFAP2Cellular oncology (Dordrecht, Netherlands) · 2024
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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

14 authors at 6 institutions in 1 country.

Jaemin LeeAging Research Institute, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Jinhoi SongAging Research Institute, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Eun-Soo KwonAging Research Institute, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Seongyea JoAging Research Institute, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Min Kyung KangDepartment of Biological Sciences, Dong-A University, Busan, South Korea.
Yeon Jeong KimDepartment of Biological Sciences, Dong-A University, Busan, South Korea.
Yeonsil HwangDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, South Korea.
Hosung BaeGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, South Korea.
Tae Heung KangDepartment of Immunology, School of Medicine, Konkuk University, Seoul, South Korea.
Suhwan ChangDepartment of Biomedical Sciences and Physiology, Asan Medical Center, University of Ulsan School of Medicine, Ulsan, South Korea.
Hee Jun ChoImmunotherapy Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Song Cheol KimDepartment of Surgery, Asan Medical Center, University of Ulsan School of Medicine, Ulsan, South Korea.
Seokho KimAging Research Institute, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Sang Seok KohDepartment of Biological Sciences, Dong-A University, Busan, South Korea.
Korea Research Institute of Bioscience and Biotechnology · KRDong-A University · KRKorea Advanced Institute of Science and Technology · KRUniversity of Ulsan · KRAsan Medical Center · KRKonkuk University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CTHRC1 (collagen triple-helix repeat-containing 1), a protein secreted during the tissue-repair process, is highly expressed in several malignant tumors, including pancreatic cancer. We recently showed that CTHRC1 has an important role in the progression and metastasis of pancreatic cancer. Although CTHRC1 secretion affects tumor cells, how it promotes tumorigenesis in the context of the microenvironment is largely unknown. Here we identified a novel role of CTHRC1 as a potent endothelial activator that promotes angiogenesis by recruiting bone marrow-derived cells to the tumor microenvironment during tumorigenesis. Recombinant CTHRC1 (rCTHRC1) enhanced endothelial cell (EC) proliferation, migration and capillary-like tube formation, which was consistent with the observed increases in neovascularization in vivo. Moreover, rCTHRC1 upregulated angiopoietin-2 (Ang-2), a Tie2 receptor ligand, through ERK-dependent activation of AP-1 in ECs, resulting in recruitment of Tie2-expressing monocytes (TEMs) to CTHRC1-overexpressing tumor tissues. Treatment with a CTHRC1-neutralizing antibody-abrogated Ang-2 expression in the ECs in vitro. Moreover, administration of a CTHRC1-neutralizing antibody to a xenograft mouse model reduced the tumor burden and infiltration of TEMs in the tumor tissues, indicating that blocking the CTHRC1/Ang-2/TEM axis during angiogenesis inhibits tumorigenesis. Collectively, our findings support the hypothesis that CTHRC1 induction of the Ang-2/Tie2 axis mediates the recruitment of TEMs, which are important for tumorigenesis and can be targeted to achieve effective antitumor responses in pancreatic cancers.

Identifiers

PMID27686285
PMCPMC5050301
OpenAlexW2526233022

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Registered trials

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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.