通过抑制PDIA3调节生物能量代谢可防止乳腺癌细胞粘附内皮细胞。

IF 5.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Marta Stojak , Kamila Wojnar-Lason , Anna Kurpinska , Patrycja Kaczara , Filip A Fedak , Joanna Suraj-Prazmowska , Martyna Stachowicz-Suhs , Joanna Rossowska , Magdalena Milczarek , Ivars Kalviņš , Joanna Wietrzyk , Stefan Chlopicki
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引用次数: 0

摘要

蛋白二硫异构酶(PDI)的表达增加,特别是PDIA3,与乳腺癌细胞的侵袭性有关。然而,PDIA3是否通过改变癌细胞的代谢来调节癌细胞的表型尚未被研究。在这里,我们研究了新型PDIA3抑制剂C-3399对乳腺癌细胞与细胞外基质(ECM)和肺微血管内皮细胞(hLMVEC)粘附的影响。此外,我们还探讨了C-3399抑制PDIA3的抗粘附作用是否可以通过细胞生物能量学的变化来介导。我们发现PDIA3抑制改变了两种人类乳腺癌细胞系(代表管腔(MCF-7)和基底(MDA-MB-231)亚型)对ECM和hLMVEC的粘附相互作用。我们证实C-3399的抗粘附作用是由于PDIA3的抑制作用,因为在PDIA3沉默的癌细胞中这种作用消失了。MCF-7和MDA-MB-231细胞表现出不同的代谢谱,MCF-7中三羧酸(TCA)循环代谢物水平较高。有趣的是,PDIA3抑制的抗粘附作用与TCA代谢物(马来酸盐、富马酸盐、α -酮戊二酸盐、异柠檬酸盐)的下调和乳酸生成的增加有关,尤其是在MCF-7细胞中。线粒体呼吸抑制剂对MCF-7细胞的抗黏附作用有明显影响,但对MDA-MB-231细胞的作用较弱。C-3399及其主要代谢物(C-3399- b)的定量揭示了活性化合物的细胞外代谢。总之,抑制细胞外PDIA3代表了一种抑制癌细胞线粒体生物能量代谢和限制乳腺癌细胞、ECM和肺内皮之间粘附信号传导的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Modulation of bioenergetic metabolism by PDIA3 inhibition prevents breast cancer cell adhesion to endothelial cells

Modulation of bioenergetic metabolism by PDIA3 inhibition prevents breast cancer cell adhesion to endothelial cells
Increased expression of protein disulphide isomerase (PDI), particularly PDIA3, is associated with breast cancer cell aggressiveness. However, it has not been explored whether PDIA3 modulates cancer cell phenotypes by altering cancer cell metabolism. Here, we investigated the effects of C-3399, a novel PDIA3 inhibitor, on the adhesion of breast cancer cells to the extracellular matrix (ECM) and pulmonary microvascular endothelial cells (hLMVEC). Additionally, we explored whether the anti-adhesive effect of PDIA3 inhibition by C-3399 could be mediated by changes in cellular bioenergetics. We found that PDIA3 inhibition modifies adhesive interactions of two human breast cancer lines, representing the luminal (MCF-7) and basal (MDA-MB-231) subtypes, to ECM and hLMVEC. We confirmed that the anti-adhesive effect of C-3399 was due to the inhibition of PDIA3, as the effect was lost in cancer cells with silenced PDIA3. MCF-7 and MDA-MB-231 cells displayed distinct metabolic profiles, with higher levels of tricarboxylic acid (TCA) cycle metabolites in MCF-7. Interestingly, the anti-adhesive effect of PDIA3 inhibition was associated with the downregulation of TCA metabolites (malate, fumarate, alpha-ketoglutarate, isocitrate) and increased lactate production, particularly in MCF-7 cells. Treatment with mitochondrial respiration inhibitors phenocopied the anti-adhesive effect in MCF-7 but had weaker effects in MDA-MB-231 cells. Quantification of C-3399 and its major metabolite (C-3399-B) revealed the extracellular metabolism of the active compound. In conclusion, the inhibition of extracellular PDIA3 represents a novel approach to inhibit the mitochondrial bioenergetic metabolism of cancer cells and to limit adhesion of cancer cells to the pulmonary endothelium.
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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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