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肉碱棕榈酰转移酶1A抑制剂替利卡通过诱导凋亡对犬乳腺癌细胞显示出有前景的抗肿瘤活性。

The Carnitine Palmitoyltransferase 1A Inhibitor Teglicar Shows Promising Antitumour Activity against Canine Mammary Cancer Cells by Inducing Apoptosis.

作者信息

Cacciola Nunzio Antonio, Sepe Fabrizia, Fioriniello Salvatore, Petillo Orsolina, Margarucci Sabrina, Scivicco Marcello, Peluso Gianfranco, Balestrieri Anna, Bifulco Giovanna, Restucci Brunella, Severino Lorella

机构信息

Department of Veterinary Medicine and Animal Production, University of Naples Federico II, Via F. Delpino 1, 80137 Naples, Italy.

Research Institute on Terrestrial Ecosystems (IRET), UOS Naples-National Research Council (CNR), Via Pietro Castellino 111, 80131 Naples, Italy.

出版信息

Pharmaceuticals (Basel). 2023 Jul 10;16(7):987. doi: 10.3390/ph16070987.

Abstract

Canine mammary tumours (CMTs) are the most common cancer in intact female dogs. In addition to surgery, additional targeted and non-targeted therapies may offer survival benefits to these patients. Therefore, exploring new treatments for CMT is a promising area in veterinary oncology. CMT cells have an altered lipid metabolism and use the oxidation of fatty acids for their energy needs. Here we investigated the tumoricidal effects of teglicar, a reversible inhibitor of carnitine palmitoyl transferase 1A (CPT1A), the rate-limiting enzyme for fatty acid import into mitochondria, on two CMT cells, P114 and CMT-U229. Viability and apoptosis were examined in CMT cells using the crystal violet assay, trypan blue assay, and flow cytometry analysis. The expression of mediators of apoptosis signalling (e.g., caspase-9, caspase-8, and caspase-3) was assessed by quantitative real-time polymerase chain reaction and western blot analyses. Teglicar was able to decrease cell viability and induce apoptosis in P114 and CMT-U229 cells. At the molecular level, the effect of teglicar was associated with an upregulation of the mRNA expression levels of , and and an increase in their protein levels. In summary, our results show that teglicar has a potential effect against CMTs through the induction of apoptotic cell death, making it a promising therapeutic agent against CMTs.

摘要

犬乳腺肿瘤(CMTs)是未绝育雌性犬最常见的癌症。除手术外,额外的靶向和非靶向治疗可能会给这些患者带来生存益处。因此,探索CMTs的新治疗方法是兽医肿瘤学中一个很有前景的领域。CMT细胞的脂质代谢发生改变,并利用脂肪酸氧化来满足其能量需求。在此,我们研究了肉碱棕榈酰转移酶1A(CPT1A,脂肪酸进入线粒体的限速酶)的可逆抑制剂替利卡对两种CMT细胞P114和CMT-U229的杀肿瘤作用。使用结晶紫测定法、台盼蓝测定法和流式细胞术分析检测CMT细胞的活力和凋亡情况。通过定量实时聚合酶链反应和蛋白质印迹分析评估凋亡信号传导介质(如半胱天冬酶-9、半胱天冬酶-8和半胱天冬酶-3)的表达。替利卡能够降低P114和CMT-U229细胞的活力并诱导其凋亡。在分子水平上,替利卡的作用与 、 和 的mRNA表达水平上调及其蛋白质水平增加有关。总之,我们的结果表明,替利卡通过诱导凋亡性细胞死亡对CMTs具有潜在作用,使其成为一种有前景的抗CMTs治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5947/10383333/2791ec467291/pharmaceuticals-16-00987-g001.jpg

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