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B7-H3 调节抗肿瘤免疫并促进结直肠癌肿瘤发展

英文原题:B7-H3 regulates anti-tumor immunity and promotes tumor development in colorectal cancer.

查看英文原题

B7-H3 regulates anti-tumor immunity and promotes tumor development in colorectal cancer.

PubMed 2023/11/28(内容时间) Biochim Biophys Acta Rev Cancer Q1 · IF 11.2(JCR 2025)

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中文摘要

结直肠癌(CRC)是胃肠道常见的恶性肿瘤,也是全球最常见的癌症相关死亡原因之一。免疫检查点抑制剂已成为许多癌症治疗的里程碑,具有显著的疗效。然而,其对结直肠癌的治疗效果仍然有限。B7-H3是B7/CD28家族的一种新型免疫检查点分子,在包括结直肠癌在内的多种实体瘤中过表达。B7-H3曾被认为是一种促进抗肿瘤免疫的共刺激分子。然而,越来越多的研究支持B7-H3是一种共抑制分子,在结直肠癌中发挥重要的免疫抑制作用。同时,B7-H3促进结直肠癌的代谢重编程、侵袭和转移以及化疗耐药。靶向B7-H3的治疗,包括单克隆抗体、抗体药物偶联物和CAR-T 细胞,具有改善结直肠癌患者预后的巨大潜力。

展开英文摘要原文

Colorectal cancer (CRC) is a common malignant tumor of the gastrointestinal tract and one of the most common causes of cancer-related deaths worldwide. Immune checkpoint inhibitors have become a milestone in many cancer treatments with significant curative effects.

However, its therapeutic effect on colorectal cancer is still limited. B7-H3 is a novel immune checkpoint molecule of the B7/CD28 family and is overexpressed in a variety of solid tumors including colorectal cancer. B7-H3 was considered as a costimulatory molecule that promotes anti-tumor immunity.

However, more and more studies support that B7-H3 is a co-inhibitory molecule and plays an important immunosuppressive role in colorectal cancer. Meanwhile, B7-H3 promoted metabolic reprogramming, invasion and metastasis, and chemoresistance in colorectal cancer. Therapies targeting B7-H3, including monoclonal antibodies, antibody drug conjugations, and chimeric antigen receptor T cells, have great potential to improve the prognosis of colorectal cancer patients.

论文信息

作者
Zhang H、Zhu M、Zhao A、Shi T、Xi Q
第一作者单位
Department of Gastroenterology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.China
通讯作者单位
Department of Gastroenterology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China. Electronic address: xqhxqhxqh@126.com.China
文献类型
综述 · 非美国政府资助研究
期刊
Biochimica et biophysica acta. Reviews on cancer2024 Jan
原文标识
PubMed 38036107 · DOI 10.1016/j.bbcan.2023.189031