Evidence map›Paper›PMID 35348270›Full record

ArticleCancer science2022

Novel cancer-specific epidermal growth factor receptor antibody obtained from the serum of esophageal cancer patients with long-term survival.

Sayaka Takagi-Maeda, Satoshi Yajima, Takashi Suzuki, Katsuaki Usami, Nobuaki Takahashi, Rinpei Niwa, Hideaki Shimada

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
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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

7 authors at 2 institutions in 1 country.

Sayaka Takagi-MaedaResearch and Development Division, Kyowa Kirin Co., Ltd., Machida-shi, Tokyo, Japan.
Satoshi YajimaDepartment of Surgery, School of Medicine, Toho University, Ota-ku, Tokyo, Japan.
Takashi SuzukiDepartment of Surgery, School of Medicine, Toho University, Ota-ku, Tokyo, Japan.
Katsuaki UsamiResearch and Development Division, Kyowa Kirin Co., Ltd., Machida-shi, Tokyo, Japan.ORCID https://orcid.org/0000-0003-2782-3392
Nobuaki TakahashiResearch and Development Division, Kyowa Kirin Co., Ltd., Chiyoda-ku, Tokyo, Japan.
Rinpei NiwaResearch and Development Division, Kyowa Kirin Co., Ltd., Machida-shi, Tokyo, Japan.
Hideaki ShimadaDepartment of Surgery, School of Medicine, Toho University, Ota-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0002-1990-8217
Kyowa Kirin (Japan) · JPToho University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although esophageal cancer has a poor prognosis after recurrence, some patients have shown long-term survival despite recurrence. We hypothesized that induction of either antitumor Abs or antitumor-specific CTLs could play a role in long-term survival (5 years or longer) in patients with recurrence and/or distant metastases. Therefore, we aimed to obtain Abs that specifically bind to cancer cells by using serum samples from patients with a good prognosis. A phage library was prepared using PBMC mRNA of the patients, and cell panning was carried out using an esophageal cancer cell line. Results showed the presence of an epidermal growth factor receptor (EGFR) Ab, KT112, that specifically bound to the cancer cell line. Notably, KT112 bound to only EGFR-positive cancer cells but failed to bind to normal esophageal cells. Furthermore, KT112 was characterized by responses to EGFR expressed on cancer cells but not to the recombinant extracellular domain of EGFR. Immunohistochemical analysis showed that KT112 reacted with 17.4% of esophageal squamous cell carcinoma tissue but not with any other cancer or normal tissue, suggesting that the Ab recognizes cancer-specific forms of EGFR and might have contributed to tumor suppression in patients with esophageal cancer. Furthermore, because of its high cancer specificity, KT112 could be a promising therapeutic option (e.g., in Ab-drug conjugates) for esophageal cancer.

Indexed as

Esophageal NeoplasmsEsophageal Squamous Cell CarcinomaErbB ReceptorsHumansLeukocytes, MononuclearErbB Receptorsantibodycancer specificityEGFResophageal squamous cell carcinomaphage display

Identifiers

PMID35348270
PMCPMC9207364
OpenAlexW4220782940

What OpenQuestion holds

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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.