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卡比多巴改变乳腺癌和黑色素瘤细胞中的色氨酸代谢,导致吲哚-3-乙腈的形成,这是一种促增殖代谢物。

Carbidopa Alters Tryptophan Metabolism in Breast Cancer and Melanoma Cells Leading to the Formation of Indole-3-Acetonitrile, a Pro-Proliferative Metabolite.

机构信息

Laboratory of Pharmacology, Department of Drug Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge Viterbo Ferreira, 228, 4050-313 Porto, Portugal.

Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Rua Júlio Amaral de Carvalho, 45, 4200-135 Porto, Portugal.

出版信息

Biomolecules. 2019 Aug 24;9(9):409. doi: 10.3390/biom9090409.

Abstract

Carbidopa is used for the treatment of Parkinson's disease (PD) as an inhibitor of DOPA decarboxylase, and PD patients taking carbidopa have a lower incidence of various tumors, except for breast cancer and melanoma. Recently, it was shown that carbidopa inhibits tryptophan-2,3-dioxygenase (TDO) and kynureninase enzymes. In the present study, the effect of carbidopa on the viability and metabolic profile of breast cancer MCF-7 and melanoma A375 cells was investigated. Carbidopa was not effective in inhibiting MCF-7 and A375 proliferation. Liquid chromatography and mass spectrometry revealed a new compound, identified as indole-3-acetonitrile (IAN), which promoted a concentration-dependent increase in the viability of both cell lines. The results suggest that treatment with carbidopa may alter tryptophan (Trp) metabolism in breast cancer and melanoma leading to the formation of a pro-proliferative Trp metabolite, which may contribute to its failure in reducing breast cancers and melanoma incidence in PD patients taking carbidopa.

摘要

卡比多巴被用作帕金森病(PD)的治疗药物,作为一种 DOPA 脱羧酶抑制剂,服用卡比多巴的 PD 患者各种肿瘤的发病率较低,除乳腺癌和黑色素瘤外。最近,研究表明卡比多巴可抑制色氨酸-2,3-双加氧酶(TDO)和犬尿氨酸酶。在本研究中,研究了卡比多巴对乳腺癌 MCF-7 和黑色素瘤 A375 细胞活力和代谢谱的影响。卡比多巴对 MCF-7 和 A375 增殖没有抑制作用。液相色谱和质谱揭示了一种新的化合物,鉴定为吲哚-3-乙腈(IAN),它促进了两种细胞系活力的浓度依赖性增加。结果表明,卡比多巴的治疗可能会改变乳腺癌和黑色素瘤中的色氨酸(Trp)代谢,导致形成促增殖的 Trp 代谢物,这可能导致其在减少服用卡比多巴的 PD 患者乳腺癌和黑色素瘤发病率方面的失败。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/6770008/af0be3c66db8/biomolecules-09-00409-g001.jpg

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