Colitis‐associated colorectal adenocarcinomas frequently express claudin 18 isoform 2: implications for claudin 18.2 monoclonal antibody therapy

克洛丹 医学 免疫组织化学 紧密连接 腺癌 癌症研究 内科学 生物 病理 癌症 细胞生物学
作者
Mai Iwaya,Hiroyuki Hayashi,Tomoyuki Nakajima,Kazuyuki Matsuda,Yasuhiro Kinugawa,Yosuke Tobe,Yoko Tateishi,Yugo Iwaya,Takeshi Uehara,Hiroyoshi Ota
出处
期刊:Histopathology [Wiley]
卷期号:79 (2): 227-237 被引量:30
标识
DOI:10.1111/his.14358
摘要

Claudin 18 (CLDN18) is a member of the claudin family of cell surface proteins, which are widely expressed in epithelial cells and play a role in cell-cell adhesion. CLDN18 isoform 2 (CLDN18.2) is specifically expressed in gastric epithelial cells, and is frequently expressed at high levels in gastric adenocarcinoma. On the basis of this, zolbetuximab, a targeted monoclonal antibody, has been developed for patients with CLDN18.2-positive gastro-oesophageal adenocarcinoma. Colitis-associated colorectal adenocarcinomas (CACs) tend to lose intestinal markers and show aberrant gastric mucin expression. Furthermore, clinical trials of human epidermal growth factor receptor 2 (HER2) inhibitor therapy for colorectal carcinoma are ongoing. However, the expression profile of CLDN18.2 and HER2 has not been described in a series of human CACs.We performed immunohistochemistry for CLDN18 and HER2 on 56 consecutive CACs from 55 inflammatory bowel disease patients, and compared the expression profile with that of a control group of 56 sporadic colorectal adenocarcinomas (CRCs). CLDN18.1 expression and CLDN18.2 expression were validated by reverse transcription polymerase chain reaction (PCR) in paraffin-embedded CRC tissues. CLDN18 was positive in 27% (15/56) of CACs and in 5% (3/56) of sporadic CRCs (P = 0.004), and CLDN18-positive CACs were more likely to have lymph node metastasis than CLDN18-negative CACs (67% versus 36%; P = 0.017). CLDN18 expression was significantly associated with MUC5AC expression (P < 0.001) and loss of special AT-rich sequence-binding protein 2 expression (P = 0.005) in CACs. CLDN18.2 was expressed in CRCs that were immunoreactive for CLDN18. Only 4% of CACs were immunoreactive for HER2, and no differences were identified in sporadic CRCs.These findings suggest that certain CAC cases may be candidates for targeted zolbetuximab therapy.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
自由大碗发布了新的文献求助10
刚刚
章半仙完成签到,获得积分10
1秒前
1秒前
独特啤酒发布了新的文献求助10
1秒前
Nico_Ding完成签到,获得积分10
1秒前
爱撒娇的怜珊完成签到,获得积分10
2秒前
轱辘牛发布了新的文献求助20
2秒前
2秒前
wu发布了新的文献求助10
2秒前
林兰完成签到,获得积分10
3秒前
123qwe完成签到,获得积分10
3秒前
慕青应助开心的问晴采纳,获得10
3秒前
lmn完成签到,获得积分10
3秒前
英勇觅夏关注了科研通微信公众号
4秒前
qz发布了新的文献求助10
4秒前
4秒前
4秒前
乐观冰巧完成签到,获得积分20
4秒前
4秒前
鹿lu发布了新的文献求助10
5秒前
awa606发布了新的文献求助10
5秒前
Lymtics发布了新的文献求助10
6秒前
无极微光应助demon采纳,获得20
6秒前
6秒前
Jqb发布了新的文献求助10
6秒前
7秒前
7秒前
杜拉拉完成签到,获得积分10
7秒前
斯文败类应助369ninja采纳,获得10
8秒前
懵懂的海露完成签到,获得积分10
8秒前
CodeCraft应助sunnie采纳,获得10
8秒前
Orange应助sunnie采纳,获得10
8秒前
linger发布了新的文献求助10
8秒前
ycp完成签到,获得积分0
8秒前
JYOHS发布了新的文献求助10
9秒前
10秒前
佳佳发布了新的文献求助10
11秒前
雷锋完成签到,获得积分10
12秒前
qz完成签到,获得积分10
12秒前
marie完成签到,获得积分10
12秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Arthritis and Related Conditions, An Issue of Orthopedic Clinics 1000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
ズームレンズの光学設計に関する研究 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7292168
求助须知:如何正确求助?哪些是违规求助? 8911140
关于积分的说明 18863722
捐赠科研通 6959278
什么是DOI,文献DOI怎么找? 3209566
关于科研通互助平台的介绍 2379066
邀请新用户注册赠送积分活动 2185369