Evidence map›Paper›PMID 35094710›Full record

ArticleDiagnostic pathology2022

Establishment of an antibody specific for AMIGO2 improves immunohistochemical evaluation of liver metastases and clinical outcomes in patients with colorectal cancer.

Keisuke Goto, Mitsuhiko Osaki, Runa Izutsu, Hiroshi Tanaka, Ryo Sasaki, Akimitsu Tanio, Hiroyuki Satofuka, Yasuhiro Kazuki, Manabu Yamamoto, Hiroyuki Kugoh and 4 more

Open access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

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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 1 institution in 1 country.

Keisuke GotoDivision of Experimental Pathology, Tottori University Faculty of Medicine, 86 Nishicho, 683-8503, Yonago, Japan.
Mitsuhiko OsakiDivision of Experimental Pathology, Tottori University Faculty of Medicine, 86 Nishicho, 683-8503, Yonago, Japan.
Runa IzutsuDivision of Experimental Pathology, Tottori University Faculty of Medicine, 86 Nishicho, 683-8503, Yonago, Japan.
Hiroshi TanakaTrans Chromosomics, Inc., 683-8503, Yonago, Tottori, Japan.
Ryo SasakiDivision of Experimental Pathology, Tottori University Faculty of Medicine, 86 Nishicho, 683-8503, Yonago, Japan.
Akimitsu TanioDivision of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Tottori University Faculty of Medicine, 683-8503, Yonago, Japan.
Hiroyuki SatofukaChromosome Engineering Research Center (CERC), Tottori University, 683-8503, Yonago, Japan.
Yasuhiro KazukiChromosome Engineering Research Center (CERC), Tottori University, 683-8503, Yonago, Japan.
Manabu YamamotoDivision of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Tottori University Faculty of Medicine, 683-8503, Yonago, Japan.
Hiroyuki KugohChromosome Engineering Research Center (CERC), Tottori University, 683-8503, Yonago, Japan.
Hisao ItoDivision of Experimental Pathology, Tottori University Faculty of Medicine, 86 Nishicho, 683-8503, Yonago, Japan.
Mitsuo OshimuraChromosome Engineering Research Center (CERC), Tottori University, 683-8503, Yonago, Japan.
Yoshiyuki FujiwaraDivision of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Tottori University Faculty of Medicine, 683-8503, Yonago, Japan.
Futoshi OkadaDivision of Experimental Pathology, Tottori University Faculty of Medicine, 86 Nishicho, 683-8503, Yonago, Japan. fuokada@tottori-u.ac.jp.
Tottori University · JP

Funding

Basis for Supporting Innovative Drug Discovery and Life Science Research of Japan Agency for Medical Research and Development JP21am0101124CREST from Japan Science and Technology Agency JPMJCR18S4The Japanese Ministry of Education, Culture, Sports, Science and Technology 20K07447The Japanese Ministry of Education, Culture, Sports, Science and Technology 20K16303
6 · The paper itself

Abstract

instructionThe human amphoterin-induced gene and open reading frame (AMIGO) was identified as a novel cell adhesion molecule of type I transmembrane protein. AMIGO2 is one of three members of the AMIGO family (AMIGO1, 2, and 3), and the similarity between them is approximately 40% at the amino acid level. We have previously shown that AMIGO2 functions as a driver of liver metastasis. Immunohistochemical analysis of AMIGO2 expression in colorectal cancer (CRC) using a commercially available anti-AMIGO2 mouse monoclonal antibody clone sc-373699 (sc mAb) correlated with liver metastasis and poor prognosis. However, the sc mAb was found to be cross-reactive with all three molecules in the AMIGO family.

methodsWe generated a rat monoclonal antibody clone rTNK1A0012 (rTNK mAb) for human AMIGO2. The rTNK mAb was used to re-evaluate the association between AMIGO2 expression and liver metastases/clinical outcomes using the same CRC tissue samples previously reported with sc mAb.

resultsWestern blot analysis revealed that a rTNK mAb was identified as being specific for AMIGO2 protein and did not cross-react with AMIGO1 and AMIGO3. The rTNK mAb and sc mAb showed higher AMIGO2 expression, which correlates with a high frequency of liver metastases (65.3% and 47.5%, respectively), while multivariate analysis showed that AMIGO2 expression was an independent prognostic factor for liver metastases (p = 7.930E-10 and p = 1.707E-5). The Kaplan-Meier analyses showed that the rTNK mAb (p = 0.004), but not sc mAb (p = 0.107), predicted worse overall survival in patients with high AMIGO2 expression. The relationship between AMIGO2 expression and poor disease-specific survival showed a higher level of significance for rTNK mAb (p = 0.00004) compared to sc mAb (p = 0.001).

conclusionsThese results indicate that the developed rTNK1A0012 mAb is an antibody that specifically recognizes AMIGO2 by immunohistochemistry and can be a more reliable and applicable method for the diagnostic detection of liver metastases and worse prognosis in patients with high AMIGO2-expressing CRC.

Indexed as

Colorectal NeoplasmsLiver NeoplasmsAnimalsHumansImmunohistochemistryMembrane ProteinsMiceNerve Tissue ProteinsPrognosisRatsAMIGO2 protein, humanAmigo2 protein, mouseAmigo3 protein, ratMembrane ProteinsNerve Tissue ProteinsAMIGO2Colorectal cancerLiver metastasisMonoclonal antibodyPrognosis

Identifiers

PMID35094710
PMCPMC8802484
OpenAlexW4225277230

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LicenceCC BY
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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.