Zheng Christy, Allen Kaelyn O, Liu Tianrui, Solodin Natalia M, Meyer Mark B, Salem Kelley, Tsourkas Phillipos K, McIlwain Sean J, Vera Jessica M, Cromwell Erika R, Ozers Mary Szatkowski, Fowler Amy M, Alarid Elaine T
McArdle Laboratory for Cancer Research, Department of Oncology, Carbone Comprehensive Cancer Center, University of Wisconsin-Madison, Madison, WI 53705, USA.
Department of Nutritional Sciences, University of Wisconsin-Madison, Madison, WI 53706, USA.
Cancers (Basel). 2024 Aug 21;16(16):2906. doi: 10.3390/cancers16162906.
Estrogen receptor (ER)-positive breast cancer is characterized by late recurrences following initial treatment. The epithelial cell fate transcription factor Grainyhead-like protein 2 (GRHL2) is overexpressed in ER-positive breast cancers and is linked to poorer prognosis as compared to ER-negative breast cancers. To understand how GRHL2 contributes to progression, GRHL2 was overexpressed in ER-positive cells. We demonstrated that elevated GRHL2 imparts plasticity with stem cell- and dormancy-associated traits. RNA sequencing and immunocytochemistry revealed that high GRHL2 not only strengthens the epithelial identity but supports a hybrid epithelial to mesenchymal transition (EMT). Proliferation and tumor studies exhibited a decrease in growth and an upregulation of dormancy markers, such as and . Mammosphere assays and flow cytometry revealed enrichment of stem cell markers CD44 and ALDH1, and increased self-renewal capacity. Cistrome analyses revealed a change in transcription factor motifs near GRHL2 sites from developmental factors to those associated with disease progression. Together, these data support the idea that the plasticity and properties induced by elevated GRHL2 may provide a selective advantage to explain the association between GRHL2 and breast cancer progression.
雌激素受体(ER)阳性乳腺癌的特征是初始治疗后复发较晚。上皮细胞命运转录因子颗粒头样蛋白2(GRHL2)在ER阳性乳腺癌中过表达,与ER阴性乳腺癌相比,其预后较差。为了解GRHL2如何促进肿瘤进展,在ER阳性细胞中过表达GRHL2。我们证明,GRHL2水平升高赋予细胞干细胞相关和休眠相关的可塑性特征。RNA测序和免疫细胞化学显示,高表达的GRHL2不仅强化上皮特性,还支持混合的上皮-间质转化(EMT)。增殖和肿瘤研究显示生长减少,休眠标志物如 和 上调。乳腺球分析和流式细胞术显示干细胞标志物CD44和醛脱氢酶1(ALDH1)富集,自我更新能力增强。顺式作用元件组分析显示,GRHL2位点附近转录因子基序从发育因子转变为与疾病进展相关的因子。总之,这些数据支持以下观点:GRHL2水平升高诱导的可塑性和特性可能提供一种选择性优势,以解释GRHL2与乳腺癌进展之间的关联。