Ilieva Kristina M, Cheung Anthony, Mele Silvia, Chiaruttini Giulia, Crescioli Silvia, Griffin Merope, Nakamura Mano, Spicer James F, Tsoka Sophia, Lacy Katie E, Tutt Andrew N J, Karagiannis Sophia N
St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London & NIHR Biomedical Research Centre at Guy's and St. Thomas' Hospitals and King's College London, Guy's Hospital, London, United Kingdom.
Breast Cancer Now Research Unit, School of Cancer and Pharmaceutical Sciences, King's College London, Guy's Cancer Centre, London, United Kingdom.
Front Immunol. 2018 Jan 10;8:1911. doi: 10.3389/fimmu.2017.01911. eCollection 2017.
Overexpression of the chondroitin sulfate proteoglycan 4 (CSPG4) has been associated with the pathology of multiple types of such as melanoma, breast cancer, squamous cell carcinoma, mesothelioma, neuroblastoma, adult and pediatric sarcomas, and some hematological cancers. CSPG4 has been reported to exhibit a role in the growth and survival as well as in the spreading and metastasis of tumor cells. CSPG4 is overexpressed in several malignant diseases, while it is thought to have restricted and low expression in normal tissues. Thus, CSPG4 has become the target of numerous anticancer treatment approaches, including monoclonal antibody-based therapies. This study reviews key potential anti-CSPG4 antibody and immune-based therapies and examines their direct antiproliferative/metastatic and immune activating mechanisms of action.
硫酸软骨素蛋白聚糖4(CSPG4)的过表达与多种类型的病理学相关,如黑色素瘤、乳腺癌、鳞状细胞癌、间皮瘤、神经母细胞瘤、成人和儿童肉瘤以及一些血液系统癌症。据报道,CSPG4在肿瘤细胞的生长和存活以及扩散和转移中发挥作用。CSPG4在几种恶性疾病中过表达,而在正常组织中被认为表达受限且较低。因此,CSPG4已成为众多抗癌治疗方法的靶点,包括基于单克隆抗体的疗法。本研究综述了关键的潜在抗CSPG4抗体和基于免疫的疗法,并研究了它们直接的抗增殖/转移和免疫激活作用机制。