Moshnikova Anna, Golijanin Borivoj, Amin Ali, Doyle Joshua, Kott Ohad, Gershman Boris, DuPont Michael, Li Yujing, Lu Xiongbin, Engelman Donald M, Andreev Oleg A, Reshetnyak Yana K, Golijanin Dragan
Physics Department, University of Rhode Island, Kingston, RI, USA.
Department of Pathology and Laboratory Medicine, The Warren Alpert Medical School of Brown University, The Miriam Hospital, Providence, RI, USA.
Front Urol. 2022;2. doi: 10.3389/fruro.2022.868919. Epub 2022 Aug 24.
Acidity is a useful biomarker for the targeting of metabolically active-cells in tumors. pH Low Insertion Peptides (pHLIPs) sense the pH at the surfaces of tumor cells and can facilitate intracellular delivery of cell-permeable and cell-impermeable cargo molecules. In this study we have shown the targeting of malignant lesions in human bladders by fluorescent pHLIP agents, intracellular delivery of amanitin toxin by pHLIP for the inhibition of urothelial cancer cell proliferation, and enhanced potency of pHLIP-amanitin for cancer cells with 17p loss, a mutation frequently present in urothelial cancers. Twenty-eight bladder specimens, from patients undergoing robotic assisted laparoscopic radical cystectomy for bladder cancer, were treated via intravesical incubation for 15-60 minutes with pHLIP conjugated to indocyanine green (ICG) or IR-800 near infrared fluorescent (NIRF) dyes at concentrations of 4-8 μM. White light cystoscopy identified 47/58 (81%) and NIRF pHLIP cystoscopy identified 57/58 (98.3%) of malignant lesions of different subtypes and stages selected for histopathological processing. pHLIP NIRF imaging improved diagnosis by 17.3% ( < 0.05). All carcinoma-in-situ cases missed by white light cystoscopy were targeted by pHLIP agents and were diagnosed by NIRF imaging. We also investigated the interactions of pHLIP-amanitin with urothelial cancer cells of different grades. pHLIP-amanitin produced concentration- and pH-dependent inhibition of the proliferation of urothelial cancer cells treated for 2 hrs at concentrations up to 4 μM. A 3-4x enhanced cytotoxicity of pHLIP-amanitin was observed for cells with a 17p loss after 2 hrs of treatment at pH6. Potentially, pHLIP technology may improve the management of urothelial cancers, including imaging of malignant lesions using pHLIP-ICG for diagnosis and surgery, and the use of pHLIP-amanitin for treatment of superficial bladder cancers via intravesical instillation.
酸度是一种用于靶向肿瘤中代谢活跃细胞的有用生物标志物。pH低插入肽(pHLIPs)可感知肿瘤细胞表面的pH值,并能促进细胞可渗透和不可渗透的货物分子的细胞内递送。在本研究中,我们展示了荧光pHLIP试剂对人膀胱恶性病变的靶向作用、pHLIP介导的鹅膏蕈碱毒素的细胞内递送以抑制尿路上皮癌细胞增殖,以及pHLIP-鹅膏蕈碱对17p缺失癌细胞(尿路上皮癌中常见的一种突变)的增强效力。对28例因膀胱癌接受机器人辅助腹腔镜根治性膀胱切除术患者的膀胱标本,用与吲哚菁绿(ICG)或IR-800近红外荧光(NIRF)染料偶联的pHLIP,以4-8μM的浓度进行膀胱内孵育15-60分钟。白光膀胱镜检查识别出47/58(81%)的不同亚型和阶段的恶性病变,而NIRF pHLIP膀胱镜检查识别出57/58(98.3%)的用于组织病理学处理的恶性病变。pHLIP NIRF成像使诊断准确率提高了17.3%(P<0.05)。所有白光膀胱镜检查遗漏的原位癌病例均被pHLIP试剂靶向,并通过NIRF成像得以诊断。我们还研究了pHLIP-鹅膏蕈碱与不同分级尿路上皮癌细胞的相互作用。pHLIP-鹅膏蕈碱在浓度高达4μM的情况下,对处理2小时的尿路上皮癌细胞增殖产生浓度和pH依赖性抑制。在pH6条件下处理2小时后,观察到pHLIP-鹅膏蕈碱对17p缺失细胞的细胞毒性增强了3-4倍。pHLIP技术可能会改善尿路上皮癌的管理,包括使用pHLIP-ICG进行恶性病变成像以用于诊断和手术,以及通过膀胱内灌注使用pHLIP-鹅膏蕈碱治疗浅表性膀胱癌。