Tianjin Key Laboratory of Acute Abdomen Disease Associated Organ Injury and ITCWM Repair, Tianjin Nankai Hospital, Tianjin, China.
NHC Key Laboratory of Biotechnology of Antibiotics, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences, No. 1 Tiantanxili, Dongcheng District, Beijing, China.
Braz J Med Biol Res. 2022 Sep 12;55:e12324. doi: 10.1590/1414-431X2022e12324. eCollection 2022.
Recombinant human peroxiredoxin-5 (hPRDX5), isolated from anti-cancer bioactive peptide (ACBPs), shows a homology of 89% with goat peroxiredoxin-5 (gPRDX5) and is reported to display anti-tumor activity in vivo. Herein, we explored the effect of hPRDX5 and the responsible mechanism in treating pancreatic cancer. Tumor-bearing mice were randomly divided into normal PBS group and treatment group (n=5; 10 mg/kg hPRDX5). Flow cytometry was employed to examine lymphocytes, myeloid-derived suppressor cell subsets, and the function proteins of natural killer (NK) cells in peripheral blood, spleen, and tumor tissues of mice. Western blot was used to measure the protein expressions of the key nodes in TLR4-MAPK-NF-κB signaling pathway. The rate of tumor suppression was 57.6% at a 10 mg/kg dose in orthotopic transplanted tumor mice. Moreover, the population of CD3+CD4+T cells, NK cells, and CD3+CD8+T cells was significantly increased in the tumor tissue of the hPRDX5 group, while the proportion of granulocytic-myeloid-derived suppressor cells decreased slightly. In addition, after treatment with hPRDX5, the percentage of NK cells in blood increased more than 4-fold. Our findings indicated that hPRDX5 effectively suppressed pancreatic cancer possibly via the TLR4-MAPK-NF-κB signaling cascade; hence hPRDX5 could be a prospective immunotherapy candidate for treating pancreatic cancer.
重组人过氧化物酶 5(hPRDX5),从抗癌生物活性肽(ACBPs)中分离出来,与山羊过氧化物酶 5(gPRDX5)具有 89%的同源性,并被报道在体内具有抗肿瘤活性。在此,我们探讨了 hPRDX5 及其在治疗胰腺癌中的作用机制。荷瘤小鼠随机分为正常 PBS 组和治疗组(n=5;10mg/kg hPRDX5)。采用流式细胞术检测小鼠外周血、脾脏和肿瘤组织中淋巴细胞、髓系来源抑制细胞亚群和自然杀伤(NK)细胞的功能蛋白。采用 Western blot 检测 TLR4-MAPK-NF-κB 信号通路中关键节点的蛋白表达。在荷原位移植瘤小鼠中,10mg/kg 剂量的肿瘤抑制率为 57.6%。此外,hPRDX5 组肿瘤组织中 CD3+CD4+T 细胞、NK 细胞和 CD3+CD8+T 细胞的比例明显增加,而粒细胞-髓系来源抑制细胞的比例略有下降。此外,用 hPRDX5 治疗后,血液中 NK 细胞的比例增加了 4 倍以上。我们的研究结果表明,hPRDX5 可能通过 TLR4-MAPK-NF-κB 信号级联有效抑制胰腺癌;因此,hPRDX5 可能成为治疗胰腺癌的一种有前景的免疫治疗候选药物。