Evidence map›Paper›PMID 26317650›Full record

ArticleOncotarget2015

An anti-EpCAM antibody EpAb2-6 for the treatment of colon cancer.

Mei-Ying Liao, Jun-Kai Lai, Mark Yen-Ping Kuo, Ruei-Min Lu, Cheng-Wei Lin, Ping-Chang Cheng, Kang-Hao Liang, Han-Chung Wu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. 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
2.0field-weighted citation impact, top 12% 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, 55 citations in OpenAlex.

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  20. Shedding light on the EpCAM: An overview.Journal of cellular physiology · 2019
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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

8 authors at 2 institutions in 1 country.

Mei-Ying LiaoInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Jun-Kai LaiInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Mark Yen-Ping KuoGraduate Institute of Clinical Dentistry, School of Dentistry, National Taiwan University, Taipei, Taiwan.
Ruei-Min LuInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Cheng-Wei LinInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Ping-Chang ChengInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Kang-Hao LiangInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Han-Chung WuInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Institute of Cellular and Organismic Biology, Academia Sinica · TWNational Taiwan University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelial cell adhesion molecule (EpCAM) is known to be overexpressed in epithelial cancers associated with enhanced malignant potential, particularly colorectal carcinoma (CRC) and head and neck squamous cell carcinoma (HNSCC). However, it is unknown whether progression of malignance can be directly inhibited by targeting EpCAM. Here, we have generated five novel monoclonal antibodies (mAbs) against EpCAM. One of these anti-EpCAM mAbs, EpAb2-6, was found to induce cancer cell apoptosis in vitro, inhibit tumor growth, and prolong the overall survival of both a pancreatic cancer metastatic mouse model and mice with human colon carcinoma xenografts. EpAb2-6 also increases the therapeutic efficacy of irinotecan, fluorouracil, and leucovorin (IFL) therapy in a colon cancer animal model and gemcitabine therapy in a pancreatic cancer animal model. Furthermore, EpAb2-6, which binds to positions Y95 and D96 of the EGF-II/TY domain of EpCAM, inhibits production of EpICD, thereby decreasing its translocation and subsequent signal activation. Collectively, our results indicate that the novel anti-EpCAM mAb can potentially be used for cancer-targeted therapy.

Indexed as

Xenograft Model Antitumor AssaysAnimalsAntibodies, MonoclonalAntigens, NeoplasmAntineoplastic Combined Chemotherapy ProtocolsApoptosisBlotting, WesternCamptothecinCell Adhesion MoleculesCell Line, TumorCell SurvivalColonic NeoplasmsDose-Response Relationship, DrugDrug SynergismEpithelial Cell Adhesion MoleculeFlow CytometryAntibodies, MonoclonalAntigens, NeoplasmCamptothecinCell Adhesion MoleculesEpithelial Cell Adhesion MoleculeFluorouracilIrinotecanLeucovorinVitamin B Complexcancer therapycolorectal carcinomaEpCAMtargeting imagingtherapeutic antibody

Identifiers

PMID26317650
PMCPMC4694806
OpenAlexW1897537981

What OpenQuestion holds

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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.