Topical application of local anesthetics to melanoma increases the efficacy of anti-PD-1 therapy.

IF 2 4区 医学 Q3 ONCOLOGY
Miroslav Tibensky, Filip Blasko, Peter Vargovic, Jana Jakubikova, Dana Cholujova, Jana Jakubechova, Boris Mravec
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Abstract

Experimental and clinical data have shown that the nervous system can significantly stimulate the initiation and progression of melanoma. In support of this, approaches that reduce the transmission of signals from peripheral nerves to effector tissues reduce the recurrence of melanoma. Therefore, we investigated the effect of topical application of the local anesthetic Pliaglis (7% lidocaine and 7% tetracaine) on the growth of melanoma induced by intradermal application of B16F0 cells in mice without treatment and in mice treated with the anti-PD-1 antibody. We found that application of Pliaglis to melanoma significantly reduced its growth and this effect was even pronounced in mice treated with the anti-PD-1 antibody. To determine the mechanisms and pathways responsible for the observed effect, the in vitro effect of incubating melanoma cells with lidocaine and/or tetracaine and the in vivo gene expression of cancer and immune-related factors, percentage of immune cells, gene expression of selected neurotransmitter receptors and nerve growth factors in melanoma tissue were studied. We found that lidocaine and tetracaine significantly reduced the viability of B16F0 cells in vitro. In mice with melanoma, Pliaglis potentiated the effect of anti-PD-1 antibody on gene expression of COX-2, IL-1β, IL-6, CCL11, F4/80, CD206, and NCR1. In addition, Pliaglis increased the gene expression of α9nACHR and 5-HT2a receptors and decreased the gene expression of nerve growth factor receptor (p75NTR) and p53. We also observed Pliaglis-mediated changes in myeloid populations. Topical application of this local anesthetic cream decreased the CD11b+Gr1- population and increased the CD11b+Gr1high population. Our data suggest that Pliaglis reduces melanoma growth through a direct effect on melanoma cells as well as through modulation of the immune response. The involvement of nervous system-related signaling in the inhibitory effect of Pliaglis on melanoma is inconclusive from our data.

局部麻醉药局部应用于黑色素瘤可提高抗pd -1治疗的疗效。
实验和临床数据表明,神经系统可以显著刺激黑色素瘤的发生和发展。为了支持这一点,减少从周围神经到效应组织的信号传递的方法减少了黑色素瘤的复发。因此,我们研究了局部麻醉Pliaglis(7%利多卡因和7%丁卡因)对未治疗小鼠和抗pd -1抗体小鼠皮内应用B16F0细胞诱导的黑色素瘤生长的影响。我们发现,将Pliaglis应用于黑色素瘤可显著降低其生长,这种效果甚至在使用抗pd -1抗体治疗的小鼠中也很明显。为了确定观察到的效果的机制和途径,我们研究了利多卡因和/或丁卡因孵育黑色素瘤细胞的体外效果,以及黑色素瘤组织中肿瘤和免疫相关因子的基因表达、免疫细胞百分比、选定的神经递质受体和神经生长因子的基因表达。我们发现利多卡因和丁卡因显著降低体外B16F0细胞的活力。在黑色素瘤小鼠中,Pliaglis增强了抗pd -1抗体对COX-2、IL-1β、IL-6、CCL11、F4/80、CD206和NCR1基因表达的影响。此外,Pliaglis增加α9nACHR和5-HT2a受体的基因表达,降低神经生长因子受体(p75NTR)和p53的基因表达。我们还观察到pliaglis介导的髓细胞群变化。局部应用该局麻膏可降低CD11b+Gr1-群,增加CD11b+Gr1高群。我们的数据表明,Pliaglis通过对黑色素瘤细胞的直接作用以及通过调节免疫反应来减少黑色素瘤的生长。从我们的数据来看,Pliaglis对黑色素瘤的抑制作用中涉及的神经系统相关信号是不确定的。
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来源期刊
Neoplasma
Neoplasma 医学-肿瘤学
CiteScore
5.40
自引率
0.00%
发文量
238
审稿时长
3 months
期刊介绍: The journal Neoplasma publishes articles on experimental and clinical oncology and cancer epidemiology.
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