Park Jun Young, Chae Ju Ri, Cho Ye Lim, Kim Youndong, Lee Dasom, Lee Jeong Kyun, Kang Won Jun
Department of Nuclear Medicine, Severance Hospital, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea.
Aptamer Sciences Inc., 172, Dolma-ro, Bundang-gu Seongnam-si, Gyeonggi-do 13605, Korea.
Pharmaceutics. 2020 Oct 18;12(10):985. doi: 10.3390/pharmaceutics12100985.
Hepatocellular carcinoma (HCC) is the most common malignancy of the liver, which can progress rapidly and has a poor prognosis. Glypican-3 (GPC3) has been proposed to be an important diagnostic biomarker and therapeutic target for HCC. Aptamers have emerged as promising drug delivery vehicles because of their high binding affinity for target molecules. Herein, we developed G12msi, a gemcitabine-incorporated DNA aptamer, targeting GPC3, and evaluated its binding specificity and anti-tumor efficacy in GPC3-overexpressing HCC cell lines and murine xenograft models. GPC3-targeted aptamers were selected by using the SELEX process and the chemotherapy drug gemcitabine was internally incorporated into the aptamer. To determine the binding affinity and internalization of the G12msi, flow cytometry and confocal microscopy were performed on GPC3-positive HepG2, Hep3B, and Huh7 cells, as well as a GPC3-negative A431 cell. The anti-tumor activities of G12msi were evaluated with in vitro and in vivo models. We found that G12msi binds to GPC3-overexpressing HCC tumor cells with high specificity and is effectively internalized. Moreover, G12msi treatment inhibited the cell proliferation of GPC3-positive HCC cell lines with minimal cytotoxicity in control A431 cells. In vivo systemic administration of G12msi significantly inhibited tumor growth of HCC HepG2 cells in xenograft models without causing toxicity. These results suggest that gemcitabine-incorporated GPC3 aptamer-based drug delivery may be a promising strategy for the treatment of HCC.
肝细胞癌(HCC)是最常见的肝脏恶性肿瘤,其病情进展迅速且预后较差。Glypican-3(GPC3)已被认为是HCC的一种重要诊断生物标志物和治疗靶点。适体因其对靶分子具有高结合亲和力,已成为有前景的药物递送载体。在此,我们开发了一种靶向GPC3的、掺入吉西他滨的DNA适体G12msi,并在GPC3过表达的HCC细胞系和小鼠异种移植模型中评估了其结合特异性和抗肿瘤疗效。通过SELEX过程筛选出靶向GPC3的适体,并将化疗药物吉西他滨掺入到适体内部。为了确定G12msi的结合亲和力和内化情况,我们对GPC3阳性的HepG2、Hep3B和Huh7细胞以及GPC3阴性的A431细胞进行了流式细胞术和共聚焦显微镜检测。通过体外和体内模型评估了G12msi的抗肿瘤活性。我们发现G12msi能以高特异性结合GPC3过表达的HCC肿瘤细胞,并能有效内化。此外,G12msi处理抑制了GPC3阳性HCC细胞系的细胞增殖,而对对照A431细胞的细胞毒性最小。在体内,对异种移植模型中的HCC HepG2细胞进行G12msi全身给药可显著抑制肿瘤生长且无毒性。这些结果表明,基于掺入吉西他滨的GPC3适体的药物递送可能是一种有前景的HCC治疗策略。