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A Rationally Designed ICAM1 Antibody Drug Conjugate for Pancreatic Cancer

机译:理性设计的ICAM1抗体药物缀合物用于胰腺癌

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摘要

Outcomes for pancreatic cancer (PC) patients remain strikingly poor with a 5‐year survival of less than 8% due to the lack of effective treatment modalities. Here, a novel precision medicine approach for PC treatment is developed, which is composed of a rationally designed tumor‐targeting ICAM1 antibody‐drug conjugate (ADC) with optimized chemical linker and cytotoxic payload, complemented with a magnetic resonance imaging (MRI)‐based molecular imaging approach to noninvasively evaluate the efficiency of ICAM1 ADC therapy. It is shown that ICAM1 is differentially overexpressed on the surface of human PC cells with restricted expression in normal tissues, enabling ICAM1 antibody to selectively recognize and target PC tumors in vivo. It is further demonstrated that the developed ICAM1 ADC induces potent and durable tumor regression in an orthotopic PC mouse model. To build a precision medicine, an MRI‐based molecular imaging approach is developed that noninvasively maps the tumoral ICAM1 expression that can be potentially used to identify ICAM1‐overexpressing PC patients. Collectively, this study establishes a strong foundation for the development of a promising ADC to address the critical need in the PC patient care.
机译:由于缺乏有效的治疗方式,胰腺癌(PC)胰腺癌(PC)患者的结果仍然缺乏5年的存活率。在这里,开发了一种新的PC治疗方法,其由具有优化的化学接头和细胞毒性有效载体的合理设计的肿瘤靶向ICAM1抗体 - 药物缀合物(ADC)组成,基于磁共振成像(MRI)。基于磁共振成像(MRI)。基础非侵入性评价ICAM1 ADC治疗效率的分子成像方法。结果表明,ICAM1在人体PC细胞表面上具有差异过表达,具有在正常组织中的受限表达,使ICAM1抗体选择性地识别和靶向体内PC肿瘤。进一步证明,开发的ICAM1 ADC在原位PC小鼠模型中诱导有效和耐用的肿瘤回归。为了构建精密药物,开发了基于MRI的分子成像方法,使得无毒地映射肿瘤ICAM1表达,其可能用于鉴定ICAM1过度抑制的PC患者。集体,这项研究为开发有前途的ADC为解决PC患者护理中的关键需求来建立强大的基础。

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