Department of Molecular Imaging and Theranostics, National Institute of Radiological Sciences, National Institutes for Quantum and Radiological Science and Technology (QST-NIRS), 4-9-1 Anagawa, Inage-ku, Chiba 263-8555, Japan.
Department of Nuclear Medicine, Cancer Institute Hospital, 3-8-31 Ariake, Koto-ku, Tokyo 135-8550, Japan.
Int J Mol Sci. 2018 Sep 29;19(10):2979. doi: 10.3390/ijms19102979.
The poor prognosis of pancreatic cancer requires the development of more effective therapy. CD147 expresses in pancreatic cancer with high incidence and has a crucial role in invasion and metastasis. We developed a fully human monoclonal antibody (059-053) with high affinity for CD147. Here we evaluated the efficacy of combined treatment using radioimmunotherapy (RIT) with Y-labeled 059-053 and gemcitabine in a BxPC-3 xenograft mouse model. Expression of CD147 and matrix metalloproteinase-2 (MMP2) in BxPC-3 tumors was evaluated. In vitro and in vivo properties of 059-053 were evaluated using In-labeled 059-053 and a pancreatic cancer model BxPC-3. Tumor volume and body weight were periodically measured in mice receiving gemcitabine, RIT, and both RIT and gemcitabine (one cycle and two cycles). High expression of CD147 and MMP2 was observed in BxPC-3 tumors and suppressed by 059-053 injection. Radiolabeled 059-053 bound specifically to BxPC-3 cells and accumulated highly in BxPC-3 tumors but low in major organs. Combined treatment using RIT with gemcitabine (one cycle) significantly suppressed tumor growth and prolonged survival with tolerable toxicity. The two-cycle regimen had the highest anti-tumor effect, but was not tolerable. Combined treatment with Y-labeled 059-053 and gemcitabine is a promising therapeutic option for pancreatic cancer.
胰腺癌预后不良,需要开发更有效的治疗方法。CD147 在高发生率的胰腺癌中表达,并在侵袭和转移中起关键作用。我们开发了一种针对 CD147 具有高亲和力的全人源单克隆抗体(059-053)。在这里,我们评估了用 Y 标记的 059-053 和吉西他滨联合放射免疫治疗(RIT)在 BxPC-3 异种移植小鼠模型中的疗效。评估了 BxPC-3 肿瘤中 CD147 和基质金属蛋白酶-2(MMP2)的表达。使用 In 标记的 059-053 和胰腺癌模型 BxPC-3 评估了 059-053 的体内外特性。在接受吉西他滨、RIT 和 RIT 联合吉西他滨(一个周期和两个周期)的小鼠中定期测量肿瘤体积和体重。在 BxPC-3 肿瘤中观察到 CD147 和 MMP2 的高表达,并被 059-053 注射抑制。放射性标记的 059-053 特异性结合 BxPC-3 细胞,并在 BxPC-3 肿瘤中高度积累,但在主要器官中积累较少。用吉西他滨进行 RIT 的联合治疗(一个周期)显著抑制肿瘤生长并延长生存期,毒性可耐受。两周期方案具有最高的抗肿瘤作用,但不可耐受。用 Y 标记的 059-053 和吉西他滨联合治疗是胰腺癌有前途的治疗选择。