277 Establishment of novel syngeneic mouse gastric cell line models for CLDN18.2 CAR-T therapy

<h3>Background</h3> Only a few syngeneic mouse cell line models are available for gastric cancer. <h3>Methods</h3> We have established a cell line from an autochthonous gastric cancer formed in the stomach of a female genetically-engineered mouse (figure 1). <h3>Results</h3> This cell line recapitulated morphological and molecular features of human intestinal gastric cancer and readily formed a tumor when injected into syngeneic mice. The cell line overexpressed the isoform 2 of claudin 18, an important molecular therapeutic target in human gastric adenocarcinomas. Anti-mouse CLDN18.2 CAR-T suppressed tumor growth and prolonged survival of mice bearing the syngeneic graft. According to mass spectrometry analysis, the cells had high CLDN18.2 content. <h3>Conclusions</h3> Thus, we have generated a useful resource for the development of immunotherapeutics. <h3>Consent</h3> Written informed consent was obtained from the patient for publication of this abstract and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.

Authors

Institutions

Publication Details

Journal
Regular and Young Investigator Award Abstracts
Published
2024-11-01
DOI
https://doi.org/10.1136/jitc-2024-sitc2024.0277
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

277 Establishment of novel syngeneic mouse gastric cell line models for CLDN18.2 CAR-T therapy

Jin Boo Jeong, Min Joon Seo, Hye Ran Kim, Hark Kyun Kim
Regular and Young Investigator Award Abstracts
CAR-T cell therapy research
article

277 Establishment of novel syngeneic mouse gastric cell line models for CLDN18.2 CAR-T therapy

Jin Boo Jeong, Min Joon Seo, Hye Ran Kim, Hark Kyun Kim
article en

Abstract

<h3>Background</h3> Only a few syngeneic mouse cell line models are available for gastric cancer. <h3>Methods</h3> We have established a cell line from an autochthonous gastric cancer formed in the stomach of a female genetically-engineered mouse (figure 1). <h3>Results</h3> This cell line recapitulated morphological and molecular features of human intestinal gastric cancer and readily formed a tumor when injected into syngeneic mice. The cell line overexpressed the isoform 2 of claudin 18, an important molecular therapeutic target in human gastric adenocarcinomas. Anti-mouse CLDN18.2 CAR-T suppressed tumor growth and prolonged survival of mice bearing the syngeneic graft. According to mass spectrometry analysis, the cells had high CLDN18.2 content. <h3>Conclusions</h3> Thus, we have generated a useful resource for the development of immunotherapeutics. <h3>Consent</h3> Written informed consent was obtained from the patient for publication of this abstract and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.

Regular and Young Investigator Award Abstracts
National Cancer Center (KR)
Zero hunger
Openalex Percentile: Top 65%
CAR-T cell therapy research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.