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直接早期生长反应-1 敲低可降低黑色素瘤活力,而不依赖有丝分裂原激活的细胞外信号相关激酶抑制。

Direct early growth response-1 knockdown decreases melanoma viability independent of mitogen-activated extracellular signal-related kinase inhibition.

机构信息

Department of Ophthalmology, Mayo Clinic, Rochester, Minnesota.

Wills Eye Hospital, Philadelphia, Pennsylvania.

出版信息

Melanoma Res. 2023 Dec 1;33(6):482-491. doi: 10.1097/CMR.0000000000000921. Epub 2023 Aug 25.

DOI:10.1097/CMR.0000000000000921
PMID:37650708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10615778/
Abstract

To investigate downstream molecular changes caused by mitogen-activated protein kinase (MEK) inhibitor treatment and further explore the impact of direct knockdown of early growth response-1 ( EGR1 ) in melanoma cell culture. RNA-sequencing (RNA-Seq) was performed to determine gene expression changes with MEK inhibitor treatment. Treatment with MEK inhibitor (trametinib) was then assessed in two cutaneous (MEL888, MEL624) and one conjunctival (YUARGE 13-3064) melanoma cell line. Direct knockdown of EGR1 was accomplished using lentiviral vectors containing shRNA. Cell viability was measured using PrestoBlueHS Cell Viability Reagent. Total RNA and protein were assessed by qPCR and SimpleWestern. RNA-Seq demonstrated a profound reduction in EGR1 with MEK inhibitor treatment, prompting further study of melanoma cell lines. Following trametinib treatment of melanoma cells, viability was reduced in both cutaneous (MEL888 26%, P  < 0.01; MEL624 27%, P  < 0.001) and conjunctival (YUARGE 13-3064 33%, P  < 0.01) melanoma compared with DMSO control, with confirmed EGR1 knockdown to 0.04-, 0.01-, and 0.16-fold DMSO-treated levels (all P  < 0.05) in MEL888, MEL624, and YUARGE 13-3064, respectively. Targeted EGR1 knockdown using shRNA reduced viability in both cutaneous (MEL624 78%, P  = 0.05) and conjunctival melanoma (YUARGE-13-3064 67%, P  = 0.02). RNA-Sequencing in MEK inhibitor-treated cells identified EGR1 as a candidate effector molecule of interest. In a malignant melanoma cell population, MEK inhibition reduced viability in both cutaneous and conjunctival melanoma with a profound downstream reduction in EGR1 expression. Targeted knockdown of EGR1 reduced both cutaneous and conjunctival melanoma cell viability independent of MEK inhibition, suggesting a key role for EGR1 in melanoma pathobiology.

摘要

为了研究丝裂原活化蛋白激酶(MEK)抑制剂治疗引起的下游分子变化,并进一步探讨在黑素瘤细胞培养中直接敲低早期生长反应-1(EGR1)的影响。进行 RNA 测序(RNA-Seq)以确定 MEK 抑制剂治疗后的基因表达变化。然后在两种皮肤(MEL888、MEL624)和一种结膜(YUARGE 13-3064)黑素瘤细胞系中评估 MEK 抑制剂(曲美替尼)的治疗效果。使用含有 shRNA 的慢病毒载体实现 EGR1 的直接敲低。使用 PrestoBlueHS 细胞活力试剂测量细胞活力。通过 qPCR 和 SimpleWestern 评估总 RNA 和蛋白质。RNA-Seq 表明 MEK 抑制剂治疗后 EGR1 明显减少,这促使进一步研究黑素瘤细胞系。在黑素瘤细胞用曲美替尼治疗后,与 DMSO 对照相比,两种皮肤(MEL888 26%,P<0.01;MEL624 27%,P<0.001)和结膜(YUARGE 13-3064 33%,P<0.01)黑素瘤细胞的活力均降低,并且在 MEL888、MEL624 和 YUARGE 13-3064 中分别证实 EGR1 敲低至 DMSO 处理水平的 0.04-、0.01-和 0.16-倍(均 P<0.05)。使用 shRNA 进行靶向 EGR1 敲低降低了两种皮肤黑素瘤(MEL624 78%,P=0.05)和结膜黑素瘤(YUARGE-13-3064 67%,P=0.02)的活力。在 MEK 抑制剂处理的细胞中进行 RNA 测序鉴定出 EGR1 是一种候选效应分子。在恶性黑素瘤细胞群中,MEK 抑制降低了两种皮肤和结膜黑素瘤的活力,下游 EGR1 表达明显降低。靶向敲低 EGR1 降低了皮肤和结膜黑素瘤细胞活力,独立于 MEK 抑制,这表明 EGR1 在黑素瘤发病机制中起关键作用。

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