Centre for Tumor Biology, Barts Cancer Institute, Cancer Research UK Centre of Excellence, Queen Mary University of London, London, United Kingdom.
Director of the Barts Pancreatic Cancer Tissue Bank, Barts Cancer Institute, Cancer Research UK Centre of Excellence, Queen Mary University of London, London, United Kingdom.
Clin Cancer Res. 2021 Mar 1;27(5):1538-1552. doi: 10.1158/1078-0432.CCR-19-2163. Epub 2021 Jan 21.
To investigate whether CEACAM7 represents a novel therapeutic target for treating pancreatic ductal adenocarcinoma (PDAC) and to generate CEACAM7-targeting CAR T cells to test this hypothesis.
We identified CEACAM7 (CGM2), a member of the CEA family of proteins with expression restricted to the colon and pancreas, as a potential CAR T-cell target for PDAC. We probed a panel of PDAC tumor sections as well as patient-derived PDAC cell cultures for CEACAM7 expression. We generated CAR-targeting CEACAM7, and assessed antitumor efficacy of CEACAM7 CAR T cells using and models.
We show here that CEACAM7 is expressed in a large subset of PDAC tumors, with low to undetectable expression in all normal tissues tested. CEACAM7 is also expressed in primary PDAC cultures isolated from patient-derived tumors, with high expression within the cancer stem cell-enriched subset. CAR T cells targeting CEACAM7 are capable of targeting antigen-expressing tumor cells, and mediate remission in patient-derived xenograft tumors.
We identify CEACAM7 as a potential therapeutic target in PDAC and describe the development of CEACAM7-targeted CAR T cells with efficacy against PDAC.
研究 CEACAM7 是否代表治疗胰腺导管腺癌(PDAC)的新治疗靶点,并生成靶向 CEACAM7 的 CAR T 细胞以验证这一假设。
我们鉴定了 CEACAM7(CGM2),一种 CEA 家族蛋白的成员,其表达仅限于结肠和胰腺,是 PDAC 的潜在 CAR T 细胞靶标。我们对一系列 PDAC 肿瘤切片以及源自患者的 PDAC 细胞培养物进行了 CEACAM7 表达检测。我们生成了靶向 CEACAM7 的 CAR,并使用 和 模型评估了靶向 CEACAM7 的 CAR T 细胞的抗肿瘤疗效。
我们在此表明,CEACAM7 在大量 PDAC 肿瘤中表达,而在所有测试的正常组织中表达水平低至无法检测。CEACAM7 也在源自患者肿瘤的原代 PDAC 培养物中表达,在富含癌症干细胞的亚群中表达水平较高。靶向 CEACAM7 的 CAR T 细胞能够靶向表达抗原的肿瘤细胞,并介导患者来源的异种移植肿瘤的缓解。
我们将 CEACAM7 鉴定为 PDAC 中的一个潜在治疗靶点,并描述了靶向 CEACAM7 的 CAR T 细胞的开发及其对 PDAC 的疗效。