North China University of Science and Technology Affiliated Hospital, Tangshan, 063000 Hebei, China.
Biomed Res Int. 2022 Jun 8;2022:7145606. doi: 10.1155/2022/7145606. eCollection 2022.
To evaluate the clinical efficacy and safety of the rCCKPE38 targeted drug in patients with colon cancer in general surgery, data of 80 patients with colon cancer who were admitted to the hospital from April 2019 to July 2021 were selected and randomly divided into the treatment group and the control group, with 40 cases in each group. Patients in the treatment group were treated with the rCCKPE38 targeted drug, and those in the control group were treated with oxaliplatin. The treatment efficiency and incidence of adverse reactions were compared between the two groups. The inverse cholecystokinin (CCK) was fused with pseudomonas aeruginosa exotoxin (PE38 toxin) through the gene amplification technique to construct a prokaryotic expression vector. Then, the rCCKPE38 was purified by Ni-nitrilotriacetate (Ni-NTA) affinity chromatography, and the antitumor activity of rCCKPE38 was verified. The results showed that the amplified rCCKPE38 sequence was correct and the pET-28a prokaryotic expression system was adopted to successfully achieve active expression. The purified recombinant protein could induce the apoptosis of colon cancer cells in vitro and inhibit tumor growth in vivo. The total effective rate in the treatment group (80%, 32/40) was higher than that in the control group (60%, 24/40) ( < 0.05). To sum up, the recombinant toxin rCCKPE38 could not only specifically adsorb the colon cancer cells with high expression of CCK2R but also effectively inhibit tumor tissue growth and proliferation. Besides, the rCCKPE38 protein had a good anticancer effect that helped effectively reduce the incidence of adverse reactions in patients, which was worthy of promoting.
为评估 rCCKPE38 靶向药物在普外科结肠癌患者中的临床疗效和安全性,选取 2019 年 4 月至 2021 年 7 月期间收治的 80 例结肠癌患者,随机分为治疗组和对照组,各 40 例。治疗组采用 rCCKPE38 靶向药物治疗,对照组采用奥沙利铂治疗。比较两组患者的治疗效果和不良反应发生率。采用基因扩增技术将反向胆囊收缩素(CCK)与铜绿假单胞菌外毒素(PE38 毒素)融合,构建原核表达载体。然后通过 Ni-亚氨基二乙酸(Ni-NTA)亲和层析法纯化 rCCKPE38,并验证 rCCKPE38 的抗肿瘤活性。结果显示,扩增的 rCCKPE38 序列正确,采用 pET-28a 原核表达系统成功实现了活性表达。纯化的重组蛋白可诱导体外结肠癌细胞凋亡,抑制体内肿瘤生长。治疗组总有效率(80%,32/40)高于对照组(60%,24/40)(<0.05)。综上所述,重组毒素 rCCKPE38 不仅可以特异性吸附 CCK2R 高表达的结肠癌细胞,还能有效抑制肿瘤组织生长和增殖。此外,rCCKPE38 蛋白具有良好的抗癌作用,有助于有效降低患者不良反应的发生率,值得推广。