Evidence map›Paper›PMID 36076991›Full record

ArticleInternational journal of molecular sciences2022

Secretory SERPINE1 Expression Is Increased by Antiplatelet Therapy, Inducing MMP1 Expression and Increasing Colon Cancer Metastasis.

Won-Tae Kim, Jeong-Yeon Mun, Seung-Woo Baek, Min-Hye Kim, Gi-Eun Yang, Mi-So Jeong, Sun Young Choi, Jin-Yeong Han, Moo Hyun Kim, Sun-Hee Leem

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

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  9. Eosinophils in Rheumatoid Arthritis: A Multifaceted Role in the Pathogenesis of the Disease.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2025
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  15. World journal of gastrointestinal oncology · 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

10 authors at 4 institutions in 1 country.

Won-Tae KimDepartment of Biomedical Sciences, Dong-A University, Busan 49315, Korea.
Jeong-Yeon MunDepartment of Biomedical Sciences, Dong-A University, Busan 49315, Korea.
Seung-Woo BaekMetabolic Regulation Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Korea.ORCID 0000-0003-4664-4162
Min-Hye KimDepartment of Biomedical Sciences, Dong-A University, Busan 49315, Korea.
Gi-Eun YangDepartment of Biomedical Sciences, Dong-A University, Busan 49315, Korea.
Mi-So JeongDepartment of Biomedical Sciences, Dong-A University, Busan 49315, Korea.
Sun Young ChoiDepartment of Cardiology, Dong-A University Hospital, Busan 49201, Korea.
Jin-Yeong HanDepartment of Laboratory Medicine, Dong-A University Hospital, Busan 49201, Korea.
Moo Hyun KimDepartment of Cardiology, Dong-A University Hospital, Busan 49201, Korea.ORCID 0000-0003-3468-6453
Sun-Hee LeemDepartment of Biomedical Sciences, Dong-A University, Busan 49315, Korea.
Dong-A University Hospital · KRDong-A University · KRDaegu Health College · KRKorea Research Institute of Bioscience and Biotechnology · KR

Funding

National Research Foundation of Korea NRF-2020R1A2C1007356National Research Foundation of Korea NRF-2022R1A2C1012173
6 · The paper itself

Abstract

Contrary to many reports that antiplatelet agents inhibit cancer growth and metastasis, new solid tumors have been reported in patients receiving long-term antiplatelet therapy. We investigated the effects of these agents directly on cancer cells in the absence of platelets to mimic the effects of long-term therapy. When four antiplatelet agents (aspirin, clopidogrel, prasugrel, and ticagrelor) were administered to colon cancer cells, cancer cell proliferation was inhibited similarly to a previous study. However, surprisingly, when cells were treated with a purinergic P2Y12 inhibitor (purinergic antiplatelet agent), the motility of the cancer cells was significantly increased. Therefore, gene expression profiles were identified to investigate the effect of P2Y12 inhibitors on cell mobility, and Serpin family 1 (SERPINE1) was identified as a common gene associated with cell migration and cell death in three groups. Antiplatelet treatment increased the level of SERPINE1 in cancer cells and also promoted the secretion of SERPINE1 into the medium. Increased SERPINE1 was found to induce MMP1 and, thus, increase cell motility. In addition, an increase in SERPINE1 was confirmed using the serum of patients who received these antiplatelet drugs. With these results, we propose that SERPINE1 could be used as a new target gene to prevent the onset and metastasis of cancer in patients with long-term antiplatelet therapy.

Indexed as

Colonic NeoplasmsPlatelet Aggregation InhibitorsHumansMatrix Metalloproteinase 1Plasminogen Activator Inhibitor 1Purinergic P2Y Receptor AntagonistsTiclopidineMatrix Metalloproteinase 1MMP1 protein, humanPlasminogen Activator Inhibitor 1Platelet Aggregation InhibitorsPurinergic P2Y Receptor AntagonistsSERPINE1 protein, humanTiclopidineantiplatelet agentscancer metastasisMMP1SERPINE1

Identifiers

PMID36076991
PMCPMC9455756
OpenAlexW4293000474

What Socratic 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 Socratic graph.