Fukushima Hiroshi, Takao Seiichiro, Furusawa Aki, Suzuki Motofumi, Yang Youfeng, Ricketts Christopher J, Kano Makoto, Okuyama Shuhei, Yamamoto Hiroshi, Kano Miyu, Ball Mark W, Choyke Peter L, Linehan W Marston, Kobayashi Hisataka
Molecular Imaging Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Int J Cancer. 2025 Jun 15;156(12):2377-2388. doi: 10.1002/ijc.35364. Epub 2025 Feb 12.
Carbonic anhydrase-9 (CA9) is highly expressed in clear cell renal cell carcinoma (ccRCC) cells despite no expression in normal kidney tissues. Thus, CA9 has been proposed as a theranostic target for radioligand therapy (RLT). However, ccRCC tends to be radioresistant and may not effectively respond to RLT. Alternatively, CA9 can be targeted for near-infrared photoimmunotherapy (NIR-PIT) of ccRCC. Here, we sought to test NIR-PIT using CA9 in a preclinical model of ccRCC to determine its potential as a therapeutic strategy. Tissue microarray analysis showed that membrane CA9 was expressed in the majority of ccRCC cases. In vitro, CA9-targeted NIR-PIT induced cell membrane damage and cell killing in all CA9-expressing ccRCC cell lines specifically, UOK154, UOK220, and UOK122. In vivo, CA9-targeted NIR-PIT significantly inhibited tumor growth and prolonged survival in UOK154 and UOK220 subcutaneous xenograft models. Notably, 70%-80% of mice achieved complete remission after a single treatment of NIR-PIT. Additionally, remaining tumors after the first NIR-PIT persistently expressed CA9, suggesting that remaining tumors can be treated with repeated NIR-PIT. Furthermore, CA9-targeted NIR-PIT induced significant cytoplasmic damages on ccRCC cells in UOK154 orthotopic xenograft models. In conclusion, CA9-targeted NIR-PIT, which allow for safe and repeated application on the same lesion, is a promising treatment for ccRCC, especially in the management of multiple primary ccRCC (e.g., von Hippel-Lindau syndrome) and oligometastatic ccRCC.
碳酸酐酶-9(CA9)在透明细胞肾细胞癌(ccRCC)细胞中高表达,而在正常肾组织中无表达。因此,CA9被提议作为放射性配体疗法(RLT)的治疗诊断靶点。然而,ccRCC往往具有放射抗性,可能对RLT没有有效反应。另外,CA9可作为ccRCC近红外光免疫疗法(NIR-PIT)的靶点。在此,我们试图在ccRCC临床前模型中测试使用CA9的NIR-PIT,以确定其作为一种治疗策略的潜力。组织微阵列分析显示,膜CA9在大多数ccRCC病例中表达。在体外,靶向CA9的NIR-PIT特异性地在所有表达CA9的ccRCC细胞系,即UOK154、UOK220和UOK122中诱导细胞膜损伤和细胞杀伤。在体内,靶向CA9的NIR-PIT在UOK154和UOK220皮下异种移植模型中显著抑制肿瘤生长并延长生存期。值得注意的是,单次NIR-PIT治疗后70%-80%的小鼠实现完全缓解。此外,首次NIR-PIT治疗后残留的肿瘤持续表达CA9,这表明残留肿瘤可以通过重复NIR-PIT治疗。此外,靶向CA9的NIR-PIT在UOK154原位异种移植模型中诱导ccRCC细胞出现显著的细胞质损伤。总之,靶向CA9的NIR-PIT能够在同一病灶上安全且重复应用,是ccRCC的一种有前景的治疗方法,尤其是在多原发性ccRCC(如冯希佩尔-林道综合征)和寡转移性ccRCC的治疗中。