Mander Sunam, Naffouje Samer A, Gao Jin, Li Weiguo, Christov Konstantin, Green Albert, Bongarzone Ernesto R, Das Gupta Tapas K, Yamada Tohru
Department of Surgery, Division of Surgical Oncology, University of Illinois College of Medicine, Chicago, IL, United States.
Department of Electrical and Computer Engineering, University of Illinois College of Engineering, Chicago, IL, United States.
Front Oncol. 2022 Jul 22;12:940001. doi: 10.3389/fonc.2022.940001. eCollection 2022.
Despite recent advances in cancer research, glioblastoma multiforme (GBM) remains a highly aggressive brain tumor as its treatment options are limited. The current standard treatment includes surgery followed by radiotherapy and adjuvant chemotherapy. However, surgery without image guidance is often challenging to achieve maximal safe resection as it is difficult to precisely discern the lesion to be removed from surrounding brain tissue. In addition, the efficacy of adjuvant chemotherapy is limited by poor penetration of therapeutics through the blood-brain barrier (BBB) into brain tissues, and the lack of tumor targeting. In this regard, we utilized a tumor-targeting cell-penetration peptide, p28, as a therapeutic agent to improve the efficacy of a current chemotherapeutic agent for GBM, and as a carrier for a fluorescence imaging agent for a clear identification of GBM. Here, we show that a near-infrared (NIR) imaging agent, ICG-p28 (a chemical conjugate of an FDA-approved NIR dye, indocyanine green ICG, and tumor-targeting p28 peptide) can preferentially localize tumors in multiple GBM animal models. Moreover, xenograft studies show that p28, as a therapeutic agent, can enhance the cytotoxic activity of temozolomide (TMZ), one of the few effective drugs for brain tumors. Collectively, our findings highlight the important role of the tumor-targeting peptide, which has great potential for intraoperative image-guided surgery and the development of new therapeutic strategies for GBM.
尽管近年来癌症研究取得了进展,但多形性胶质母细胞瘤(GBM)仍然是一种极具侵袭性的脑肿瘤,因为其治疗选择有限。目前的标准治疗包括手术,随后进行放疗和辅助化疗。然而,没有图像引导的手术往往难以实现最大程度的安全切除,因为很难精确区分要从周围脑组织中切除的病变。此外,辅助化疗的疗效受到治疗药物透过血脑屏障(BBB)进入脑组织的能力差以及缺乏肿瘤靶向性的限制。在这方面,我们利用一种肿瘤靶向细胞穿透肽p28作为治疗剂,以提高当前用于GBM的化疗药物的疗效,并作为荧光成像剂的载体,以便清晰识别GBM。在此,我们表明近红外(NIR)成像剂ICG-p28(一种FDA批准的近红外染料吲哚菁绿ICG与肿瘤靶向p28肽的化学偶联物)可以在多种GBM动物模型中优先定位肿瘤。此外,异种移植研究表明,作为治疗剂的p28可以增强替莫唑胺(TMZ)的细胞毒性活性,替莫唑胺是少数几种对脑肿瘤有效的药物之一。总的来说,我们的研究结果突出了肿瘤靶向肽的重要作用,其在术中图像引导手术和GBM新治疗策略的开发方面具有巨大潜力。