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局部麻醉药利多卡因诱导基因、生长分化因子 15 抑制癌细胞系的生长。

Local anesthetic lidocaine-inducible gene, growth differentiation factor-15 suppresses the growth of cancer cell lines.

机构信息

Intensive Care Unit, Gunma University Hospital, 3-39-15, Showa-machi, Maebashi, Gunma, 371-8511, Japan.

Division of Integrated Oncology Research, Initiative for Advanced Research, Gunma University, 3-39-15, Showa-machi, Maebashi, Gunma, 371-8511, Japan.

出版信息

Sci Rep. 2022 Aug 25;12(1):14520. doi: 10.1038/s41598-022-18572-3.

DOI:10.1038/s41598-022-18572-3
PMID:36008442
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9411556/
Abstract

Administration of local anesthetics, such as lidocaine, in the perioperative period improves outcomes of cancer patients. However, its precise mechanism is still unresolved. The growth of human cancer cell lines, including HeLa cells, are suppressed by lidocaine treatment. We identified that growth differentiation factor-15 (GDF-15) was commonly upregulated in lidocaine-treated cancer cell lines. GDF-15 is a divergent member of the transforming growth factor-β (TGF-β) superfamily and it is produced as an unprocessed pro-protein form and then cleaved to generate a mature form. In lidocaine-treated HeLa cells, increased production of GDF-15 in the endoplasmic reticulum (ER) was observed and unprocessed pro-protein form of GDF-15 was secreted extracellularly. Further, lidocaine induced apoptosis and apoptosis-inducible Tribbles homologue 3 (TRIB3) was also commonly upregulated in lidocaine-treated cancer cell lines. In addition, transcription factor C/EBP homologous protein (CHOP), which is a positive regulator of not only GDF-15 but TRIB3 was also induced by lidocaine. Lidocaine-induced growth suppression and apoptosis was suppressed by knockdown of GDF-15 or TRIB3 expression by small interference RNA (siRNA). These observations suggest that lidocaine suppresses the growth of cancer cells through increasing GDF-15 and TRIB3 expression, suggesting its potential application as cancer therapy.

摘要

围手术期局部麻醉剂(如利多卡因)的应用可改善癌症患者的预后。然而,其确切机制仍未解决。利多卡因处理可抑制人癌细胞系(包括 HeLa 细胞)的生长。我们发现,生长分化因子-15(GDF-15)在利多卡因处理的癌细胞系中普遍上调。GDF-15 是转化生长因子-β(TGF-β)超家族的一个分化成员,它以未加工的前蛋白形式产生,然后被切割生成成熟形式。在利多卡因处理的 HeLa 细胞中,观察到内质网(ER)中 GDF-15 的产量增加,并且 GDF-15 的未加工前蛋白形式被分泌到细胞外。此外,利多卡因诱导细胞凋亡,并且凋亡诱导 Tribbles 同源物 3(TRIB3)在利多卡因处理的癌细胞系中也普遍上调。此外,转录因子 C/EBP 同源蛋白(CHOP)不仅是 GDF-15 的正调节剂,也是 TRIB3 的正调节剂,也被利多卡因诱导。通过小干扰 RNA(siRNA)敲低 GDF-15 或 TRIB3 的表达,可抑制利多卡因诱导的生长抑制和细胞凋亡。这些观察结果表明,利多卡因通过增加 GDF-15 和 TRIB3 的表达来抑制癌细胞的生长,提示其在癌症治疗中的潜在应用。

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e6/9411556/314b9ed162d9/41598_2022_18572_Fig6_HTML.jpg
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