Evidence map›Paper›PMID 25268742›Full record

ArticleOncotarget2014

Therapeutic effect of a TM4SF5-specific monoclonal antibody against colon cancer in a mouse model.

Young-Eun Kim, Sanghoon Kwon, Guang Wu, Dongbum Kim, Byoung Kwon Park, Jeong-A Park, Kyung-Chan Choi, Doo-Sik Kim, Hyung-Joo Kwon, Younghee Lee

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Testing the Effectiveness ofInternational journal of molecular sciences · 2020
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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 2 institutions in 1 country.

Young-Eun KimDepartment of Biochemistry, College of Natural Sciences, Chungbuk National University, Chungbuk, Republic of Korea. These authors contributed equally to this work.
Sanghoon KwonCenter for Medical Science Research, College of Medicine, Hallym University, Gangwon-do, Republic of Korea. These authors contributed equally to this work.
Guang WuCenter for Medical Science Research, College of Medicine, Hallym University, Gangwon-do, Republic of Korea. These authors contributed equally to this work.
Dongbum KimCenter for Medical Science Research, College of Medicine, Hallym University, Gangwon-do, Republic of Korea.
Byoung Kwon ParkDepartment of Microbiology, College of Medicine, Hallym University, Gangwon-do, Republic of Korea.
Jeong-A ParkDepartment of Biochemistry, College of Natural Sciences, Chungbuk National University, Chungbuk, Republic of Korea.
Kyung-Chan ChoiDepartment of Pathology, College of Medicine, Hallym University, Gangwon-do, Republic of Korea.
Doo-Sik KimDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
Hyung-Joo KwonCenter for Medical Science Research, College of Medicine, Hallym University, Gangwon-do, Republic of Korea. Department of Microbiology, College of Medicine, Hallym University, Gangwon-do, Republic of Korea.
Younghee LeeDepartment of Biochemistry, College of Natural Sciences, Chungbuk National University, Chungbuk, Republic of Korea.
Hallym University · KRChungbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transmembrane 4 superfamily member 5 protein (TM4SF5) is presumed to serve as a molecular target to prevent or treat hepatocellular carcinoma (HCC) and colon cancer in a mouse model. Previously, we reported the efficacy of anti-cancer peptide vaccine targeting TM4SF5. In addition, we reported an anti-proliferative effect of anti-TM4SF5 monoclonal antibody in HCC. Here, we investigated expression of TM4SF5 in 45 primary colon cancer tissues. Almost all of the colon cancer tissues expressed TM4SF5 based on immunohistochemistry using anti-TM4SF5 monoclonal antibody. The treatment of human colon cancer cells with anti-TM4SF5 antibody reduced growth of TM4SF5 expressing cells and enhanced expression of E-cadherin and β-catenin. Using mouse colon cancer models, we then evaluated the in vivo anti-cancer effect of anti-TM4SF5 antibody. Injection of the antibody significantly reduced growth of tumors priorly established by subcutaneous injection of human colon cancer cells HT-29 in a xenograft setting. We obtained similar results with mouse colon cancer cell line CT-26 in an allograft setting. Therefore, we suggest that the TM4SF5-specific monoclonal antibody has a therapeutic effect against colon cancer.

Indexed as

AdultAgedAnimalsAntibodies, MonoclonalAntigens, CDAntineoplastic Agentsbeta CateninCadherinsCell ProliferationColorectal NeoplasmsFemaleHCT116 CellsHT29 CellsHumansMaleMembrane ProteinsAntibodies, MonoclonalAntigens, CDAntineoplastic Agentsbeta CateninCadherinsCDH1 protein, humanCTNNB1 protein, humanMembrane ProteinsTM4SF5 protein, humanTM4SF5 protein, mouse

Identifiers

PMID25268742
PMCPMC4226692
OpenAlexW1551330852

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.