Martin-Vega Ana, Earnest Svetlana A, Augustyn Alexander, Wichaidit Chonlarat, Girard Luc, Peyton Michael, Minna John D, Johnson Jane E, Cobb Melanie H
Department of Pharmacology, UT Southwestern Medical Center, Dallas, Texas.
Hamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, Texas.
Mol Cancer Ther. 2024 Dec 3;23(12):1789-1800. doi: 10.1158/1535-7163.MCT-24-0355.
The transcription factor achaete-scute complexhomolog 1 (ASCL1) is a lineage oncogene that is central in growth and survival of the majority of small cell lung cancers and neuroendocrine (NE) non-small cell lung cancers (NSCLC) that express it. Targeting ASCL1, or its downstream pathways, remains a challenge. Small cell lung cancers and NSCLC-NE that express ASCL1 exhibit relatively low ERK1/2 activity, in dramatic contrast to NSCLCs in which the ERK pathway plays a major role in pathogenesis. ERK1/2 inhibition in ASCL1-expressing lung tumor cells revealed downregulation of ERK1/2 pathway suppressors SPRY4, SPRED1, DUSP6, and the transcription factor ETV5, which regulates DUSP6. Chromatin immunoprecipitation sequencing demonstrated that these genes are bound by ASCL1. Availability of a pharmacologic inhibitor directed mechanistic studies toward DUSP6, an ERK1/2-selective phosphatase, in a subset of ASCL1-high NE lung tumors. Inhibition of DUSP6 increased active ERK1/2, which accumulated in the nucleus. Pharmacologic and genetic inhibition of DUSP6 reduced proliferation and survival of these cancers. Resistance developed in DUSP6-knockout cells, indicating a bypass mechanism. Although targeting ASCL1 remains a challenge, our findings suggest that expression of ASCL1, DUSP6, and low phospho-ERK1/2 identifies NE lung cancers for which DUSP6 may be a therapeutic target.
转录因子无刚毛 - 小盾片复合体同源物1(ASCL1)是一种谱系癌基因,在大多数表达它的小细胞肺癌和神经内分泌(NE)非小细胞肺癌(NSCLC)的生长和存活中起核心作用。靶向ASCL1或其下游通路仍然是一个挑战。表达ASCL1的小细胞肺癌和NSCLC - NE表现出相对较低的ERK1/2活性,这与ERK通路在发病机制中起主要作用的NSCLC形成鲜明对比。对表达ASCL1的肺肿瘤细胞中的ERK1/2抑制作用揭示了ERK1/2通路抑制因子SPRY4、SPRED1、DUSP6以及调节DUSP6的转录因子ETV5的下调。染色质免疫沉淀测序表明这些基因与ASCL1结合。在一部分ASCL1高表达的NE肺肿瘤中,一种针对ERK1/2选择性磷酸酶DUSP6的药理抑制剂可用于进行机制研究。抑制DUSP6会增加活性ERK1/2,其在细胞核中积累。对DUSP6的药理和基因抑制作用降低了这些癌症的增殖和存活率。DUSP6基因敲除细胞产生了耐药性,表明存在一种旁路机制。尽管靶向ASCL1仍然是一个挑战,但我们的研究结果表明,ASCL1、DUSP6的表达以及低磷酸化ERK1/2可识别出DUSP6可能成为治疗靶点的NE肺癌。