Shukla Vivek, Rao Mahadev, Zhang Hongen, Beers Jeanette, Wangsa Darawalee, Wangsa Danny, Buishand Floryne O, Wang Yonghong, Yu Zhiya, Stevenson Holly S, Reardon Emily S, McLoughlin Kaitlin C, Kaufman Andrew S, Payabyab Eden C, Hong Julie A, Zhang Mary, Davis Sean, Edelman Daniel, Chen Guokai, Miettinen Markku M, Restifo Nicholas P, Ried Thomas, Meltzer Paul A, Schrump David S
Thoracic Epigenetics Section, Thoracic and Gastrointestinal Oncology Branch, Center for Cancer Research, NCI, Rockville, Maryland.
Genetics Branch, Center for Cancer Research, NCI, Rockville, Maryland.
Cancer Res. 2017 Nov 15;77(22):6267-6281. doi: 10.1158/0008-5472.CAN-17-0570. Epub 2017 Sep 21.
In this study, we generated induced pluripotent stem cells (iPSC) from normal human small airway epithelial cells (SAEC) to investigate epigenetic mechanisms of stemness and pluripotency in lung cancers. We documented key hallmarks of reprogramming in lung iPSCs (Lu-iPSC) that coincided with modulation of more than 15,000 genes relative to parental SAECs. Of particular novelty, we identified the PRC2-associated protein, ASXL3, which was markedly upregulated in Lu-iPSCs and small cell lung cancer (SCLC) lines and clinical specimens. overexpression correlated with increased genomic copy number in SCLC lines. silencing inhibited proliferation, clonogenicity, and teratoma formation by Lu-iPSCs, and diminished clonogenicity and malignant growth of SCLC cells Collectively, our studies validate the utility of the Lu-iPSC model for elucidating epigenetic mechanisms contributing to pulmonary carcinogenesis and highlight ASXL3 as a novel candidate target for SCLC therapy. .
在本研究中,我们从正常人小气道上皮细胞(SAEC)中生成了诱导多能干细胞(iPSC),以研究肺癌中干性和多能性的表观遗传机制。我们记录了肺iPSC(Lu-iPSC)重编程的关键特征,这些特征与相对于亲代SAEC超过15000个基因的调控相一致。特别新颖的是,我们鉴定出了与PRC2相关的蛋白ASXL3,其在Lu-iPSC、小细胞肺癌(SCLC)细胞系和临床标本中显著上调。在SCLC细胞系中,ASXL3的过表达与基因组拷贝数增加相关。ASXL3的沉默抑制了Lu-iPSC的增殖、克隆形成能力和畸胎瘤形成,并降低了SCLC细胞的克隆形成能力和恶性生长。总体而言,我们的研究验证了Lu-iPSC模型在阐明促成肺癌发生的表观遗传机制方面的效用,并突出了ASXL3作为SCLC治疗的新候选靶点。