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通过干预线粒体氧化应激和阻断 DuCLOX 信号转导,重新利用 PDE-5 抑制剂在癌症化学预防中的作用机制。

Repurposing mechanistic insight of PDE-5 inhibitor in cancer chemoprevention through mitochondrial-oxidative stress intervention and blockade of DuCLOX signalling.

机构信息

Department of Pharmaceutical Sciences, Babasaheb Bhimrao Ambedkar University, (A Central University), Vidya Vihar, Raebareli road, Lucknow, UP, 226 025, India.

Department of Pharmaceutical Sciences, King Faisal University, Al-Ahsa, Saudi Arabia.

出版信息

BMC Cancer. 2019 Oct 24;19(1):996. doi: 10.1186/s12885-019-6152-9.

Abstract

BACKGROUND

This study evaluates the anti-cancer effects of Tadalafil (potent PDE-5 inhibitor) in female albino wistar rats against n-methyl n-nitrosourea induced mammary gland carcinogenesis.

METHODS

The animals were selected and randomly divided among four groups and each group contains six animals per group. The animal tissue and serum samples were evaluated for the presence of antioxidant parameters and the cellular morphology was studied using carminic staining, haematoxylin staining and scanning electron microscopy followed by immunoblotting analysis.

RESULTS

On the grounds of hemodynamic recordings and morphology, n-methyl n-nitrosourea treated group showed distorted changes along with distorted morphological parameters. For morphological analysis, the mammary gland tissues were evaluated using scanning electron microscopy, whole mount carmine staining, haematoxylin and eosin staining. The serum samples were evaluated for the evaluation of oxidative stress markers and inflammatory markers. The level of caspase 3 and 8 were also evaluated for the estimation of apoptosis. The fatty acid profiling of mammary gland tissue was evaluated using fatty acid methyl esters formation. The mitochondrial mediated apoptosis and inflammatory markers were evaluated using immunoblotting assay.

CONCLUSION

The results confirm that Tadalafil treatment restored all the biological markers to the normal and its involvement in mitochondrial mediated death apoptosis pathway along with inhibition of inflammatory markers.

摘要

背景

本研究评估了他达拉非(强效 PDE-5 抑制剂)在雌性白化 Wistar 大鼠对 N-甲基-N-亚硝基脲诱导的乳腺致癌作用中的抗癌作用。

方法

选择动物并随机分为四组,每组包含六只动物。评估动物组织和血清样本中抗氧化参数的存在,并使用丽春红染色、苏木精染色和扫描电子显微镜进行细胞形态学研究,随后进行免疫印迹分析。

结果

根据血流动力学记录和形态学,N-甲基-N-亚硝脲处理组表现出扭曲的变化,同时伴有扭曲的形态学参数。对于形态学分析,使用扫描电子显微镜、整体胭脂红染色、苏木精和伊红染色评估乳腺组织。评估血清样本以评估氧化应激标志物和炎症标志物。还评估了半胱天冬酶 3 和 8 的水平以评估细胞凋亡。使用脂肪酸甲酯形成评估乳腺组织的脂肪酸谱。使用免疫印迹分析评估线粒体介导的细胞凋亡和炎症标志物。

结论

结果证实,他达拉非治疗将所有生物标志物恢复到正常水平,其参与线粒体介导的细胞凋亡途径,并抑制炎症标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afa1/6814136/d82b85c06fc5/12885_2019_6152_Fig1_HTML.jpg

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