Abstract 833: A novel anti-CEACAM6 heavy-chain antibody-drug conjugate for gastrointestinal cancer therapy

IF 12.5 1区 医学 Q1 ONCOLOGY
Ming-Heng Wu, Yao-Tsung Tsai, Chee Voon Yap
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引用次数: 0

Abstract

Antibody-drug conjugates (ADCs) are "biological missiles" that utilize a chemical linker to connect monoclonal antibodies (mAbs) with cytotoxic drugs, which induces the precise killing of targeted tumor cells and causes the death of surrounding untargeted cancer cells through the bystander effect. However, current ADCs are too specific to certain cancer subtypes and not specific enough to accurately target a cancer-specific protein, which limits the therapeutic populations and induces unwanted side effects. We developed a heavy-chain antibody (HCAb) from a llama immune library, which recognizes glycosylated CEACAM6 (Carcinoembryonic antigen-related cell adhesion molecule 6), a broad-surface marker of epithelial-type cancers. The anti-CEACAM6 HCAb showed a higher affinity (KD: sub-nanomolar), better thermal stability, unique tissue penetration and epitope-recognition abilities compared to the conventional antibodies. The anti-CEACAM6 HCAb-drug conjugate (HCAb-ADC), which links the HCAb and tubulin inhibitors via hydrophilic linkers, specifically killed CEACAM6-expressing colorectal (CRC), lung, pancreas, and bile duct carcinoma cells at sub-nanomolar concentrations and had a better anti-cancer effect than current FDA-approved ADCs. In xenograft models, a single administration of HCAb-ADC completely abolished colorectal and pancreatic tumors. Notably, HCAb-ADC can effectively inhibit tumor growth even at very low doses (0.2 mg/Kg) and demonstrated a superior therapeutic effect over current therapeutic regimens. Meanwhile, it exhibited minimal toxicity to normal epithelial and peripheral blood mononuclear cells. In summary, the excellent anti-tumor activity across different epithelial cancers and minimal toxicity to normal tissues support the clinical development of the novel HCAb-ADC for treating multiple epithelial-type cancers, including CRC, lung, pancreatic, and bile duct carcinoma. Citation Format: Ming-Heng Wu, Yao-Tsung Tsai, Chee Voon Yap. A novel anti-CEACAM6 heavy-chain antibody-drug conjugate for gastrointestinal cancer therapy [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular s); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1): nr 833.
833:一种用于胃肠道肿瘤治疗的新型抗ceacam6重链抗体-药物偶联物
抗体-药物偶联物(adc)是一种“生物导弹”,利用化学连接剂将单克隆抗体(mab)与细胞毒性药物连接起来,诱导靶向肿瘤细胞的精确杀伤,并通过旁观者效应导致周围非靶向癌细胞的死亡。然而,目前的adc对某些癌症亚型的特异性太强,不足以准确靶向癌症特异性蛋白,这限制了治疗人群并诱发了不必要的副作用。我们从骆驼免疫文库中开发了一种重链抗体(HCAb),该抗体识别糖基化的CEACAM6(癌胚抗原相关细胞粘附分子6),这是一种上皮型癌症的宽表面标记物。与常规抗体相比,抗ceacam6 HCAb具有更高的亲和力(KD:亚纳摩尔)、更好的热稳定性、独特的组织穿透性和表位识别能力。抗ceacam6 HCAb-药物偶联物(HCAb- adc)通过亲水连接HCAb和微管蛋白抑制剂,以亚纳摩尔浓度特异性杀死表达ceacam6的结直肠癌(CRC)、肺癌、胰腺癌和胆管癌细胞,具有比目前fda批准的adc更好的抗癌效果。在异种移植模型中,单次给药HCAb-ADC完全消除结直肠和胰腺肿瘤。值得注意的是,即使在非常低的剂量(0.2 mg/Kg)下,HCAb-ADC也能有效抑制肿瘤生长,并且比目前的治疗方案显示出更好的治疗效果。同时,对正常上皮细胞和外周血单核细胞的毒性很小。综上所述,新型HCAb-ADC在不同上皮性癌症中的出色抗肿瘤活性和对正常组织的最小毒性支持了其治疗多种上皮型癌症的临床发展,包括结直肠癌、肺癌、胰腺癌和胆管癌。引用格式:吴明恒,蔡耀宗,叶志云。一种用于胃肠道肿瘤治疗的新型抗ceacam6重链抗体-药物偶联物[摘要]。摘自:《2025年美国癌症研究协会年会论文集》;第1部分(常规);2025年4月25日至30日;费城(PA): AACR;中国癌症杂志,2015;35(8):833 - 833。
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来源期刊
Cancer research
Cancer research 医学-肿瘤学
CiteScore
16.10
自引率
0.90%
发文量
7677
审稿时长
2.5 months
期刊介绍: Cancer Research, published by the American Association for Cancer Research (AACR), is a journal that focuses on impactful original studies, reviews, and opinion pieces relevant to the broad cancer research community. Manuscripts that present conceptual or technological advances leading to insights into cancer biology are particularly sought after. The journal also places emphasis on convergence science, which involves bridging multiple distinct areas of cancer research. With primary subsections including Cancer Biology, Cancer Immunology, Cancer Metabolism and Molecular Mechanisms, Translational Cancer Biology, Cancer Landscapes, and Convergence Science, Cancer Research has a comprehensive scope. It is published twice a month and has one volume per year, with a print ISSN of 0008-5472 and an online ISSN of 1538-7445. Cancer Research is abstracted and/or indexed in various databases and platforms, including BIOSIS Previews (R) Database, MEDLINE, Current Contents/Life Sciences, Current Contents/Clinical Medicine, Science Citation Index, Scopus, and Web of Science.
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