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C 型利钠肽(CNP)通过调节瑞士白化小鼠的炎症反应抑制 7,12-二甲基苯并[a]蒽(DMBA)/巴豆油诱导的皮肤肿瘤生长。

C-type natriuretic peptide (CNP) inhibits 7,12-Dimethylbenz[a]anthracene (DMBA)/Croton oil-induced skin tumor growth by modulating inflammation in Swiss albino mice.

机构信息

Peptide Research and Molecular Cardiology Laboratory, Department of Biochemistry, Guindy Campus, University of Madras, Chennai, Tamil Nadu, India.

出版信息

J Biochem Mol Toxicol. 2023 Oct;37(10):e23423. doi: 10.1002/jbt.23423. Epub 2023 Jun 23.

Abstract

C-type natriuretic peptide (CNP) exhibits anti-inflammatory activity besides its natriuretic and diuretic functions. The present study aimed to determine the anticancer and synergistic therapeutic activity of CNP against a 7,12-Dimethylbenz[a]anthracene (DMBA)/Croton oil-induced skin tumor mouse model. CNP (2.5 µg/kg body weight) was injected either alone and/or in combination with Cisplatin (CDDP) (2 mg/kg body weight) for 4 weeks. The dorsal skin tumor incidences/growth and mortality rate were recorded during the experimental period of 16 weeks. The serum C-reactive protein (CRP), and lactate dehydrogenase (LDH) levels, infiltrating mast cells, and AgNORs proliferating cells count were analyzed in control and experimental mice. Further, the expression profile of marker genes of proliferation, inflammation, and progression molecules were analyzed using Reverse transcriptase-polymerase chain reaction (RT-PCR)/quantitative PCR (qPCR), western blot, and immunohistochemistry. The DMBA/Croton oil-induced mice exhibited 100% tumor incidence. Whereas, CNP alone, CDDP alone, and CNP+CDDP combination-treated mice exhibited 58%, 46%, and 24% tumor incidence, respectively. Also, a marked reduction in the levels of serum CRP and LDH, the number of infiltrating mast cells count and AgNORs proliferating cells count were noticed in the mice skin sections. Further, a significant reduction in both mRNA and protein expression levels of proliferation, inflammation, and progression markers were noticed in CNP (p < 0.01), CDDP (p < 0.01), and CNP+CDDP combination (p < 0.001) treated mice, respectively. The results of the present study suggest that CNP has anticancer activity. Further, the CNP+CDDP treatment has more promising anticancer activity as compared with CNP or CDDP alone treatment, probably due to the synergistic antiproliferative and anti-inflammatory activities of CNP and CDDP.

摘要

C 型利钠肽(CNP)除了具有利钠和利尿作用外,还具有抗炎活性。本研究旨在确定 CNP 对 7,12-二甲基苯并[a]蒽(DMBA)/巴豆油诱导的皮肤肿瘤小鼠模型的抗癌和协同治疗活性。CNP(2.5μg/kg 体重)单独或与顺铂(CDDP)(2mg/kg 体重)联合注射,共 4 周。在 16 周的实验期间,记录背部皮肤肿瘤的发生率/生长和死亡率。分析对照组和实验组小鼠的血清 C 反应蛋白(CRP)和乳酸脱氢酶(LDH)水平、浸润肥大细胞和 AgNORs 增殖细胞计数。进一步使用逆转录聚合酶链反应(RT-PCR)/定量 PCR(qPCR)、western blot 和免疫组织化学分析增殖、炎症和进展分子的标记基因表达谱。DMBA/巴豆油诱导的小鼠 100%发生肿瘤。而 CNP 单独、CDDP 单独和 CNP+CDDP 联合治疗的小鼠肿瘤发生率分别为 58%、46%和 24%。此外,还观察到血清 CRP 和 LDH 水平、浸润肥大细胞计数和 AgNORs 增殖细胞计数显著减少。进一步,在 CNP(p<0.01)、CDDP(p<0.01)和 CNP+CDDP 联合(p<0.001)治疗的小鼠中,增殖、炎症和进展标记物的 mRNA 和蛋白表达水平均显著降低。本研究结果表明,CNP 具有抗癌活性。此外,与 CNP 或 CDDP 单独治疗相比,CNP+CDDP 治疗具有更有前景的抗癌活性,这可能是由于 CNP 和 CDDP 的协同抗增殖和抗炎活性。

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