Cabergoline as a Novel Strategy for Post-Pregnancy Breast Cancer Prevention in Mice and Human

N. García-Sancha, R. Corchado-Cobos, A. Blanco-Gómez, O. C. Puértolas, Mercè Marzo-Castillejo, Sonia Castillo-Lluva, D. Alonso-López, Javier De Las Rivas, Julio Pozo, Alberto Orfao, Luis Valero-Juan, Carmen Patino-Alonso, David Perera, Ashok R. Venkitaraman, J. Mao, Hang Chang, Marina Mendiburu-Eliçabe, Patricia González-García, Eduardo Caleiras, Isabel Peset, M. B. G. Cenador, F. J. García-Criado, J. Pérez-Losada
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Abstract

Abstract Post-pregnancy breast cancer often carries a poor prognosis, posing a major clinical challenge. The increasing trend of later-life pregnancies exacerbates this risk, highlighting the need for effective chemoprevention strategies. Current options, limited to selective estrogen receptor modulators, aromatase inhibitors, or surgical procedures, offer limited efficacy and considerable side effects. Here, we report that cabergoline, a dopaminergic agonist, reduces the risk of breast cancer post-pregnancy in a Brca1/P53 -deficient mouse model, with implications for human breast cancer prevention. We show that a single dose of cabergoline administered post-pregnancy significantly delayed the onset and reduced the incidence of breast cancer in Brca1/P53 -deficient mice. Histological analysis revealed a notable acceleration in post-lactational involution over the short term, characterized by increased apoptosis and altered gene expression related to ion transport. Over the long term, histological changes in the mammary gland included a reduction in the ductal component, decreased epithelial proliferation, and a lower presence of recombinant Brca1/P53 target cells, which are precursors of tumors. These changes serve as indicators of reduced breast cancer susceptibility. Additionally, RNA sequencing identified gene expression alterations associated with decreased proliferation and mammary gland branching. Our findings highlight a mechanism wherein cabergoline enhances the protective effect of pregnancy against breast cancer by potentiating postlactational involution. Notably, a retrospective cohort study in women demonstrated a markedly lower incidence of post-pregnancy breast cancer in those treated with cabergoline compared to a control group. Our work underscores the importance of enhancing postlactational involution as a strategy for breast cancer prevention, and identifies cabergoline as a promising, low-risk option in breast cancer chemoprevention. This strategy has the potential to revolutionize breast cancer prevention approaches, particularly for women at increased risk due to genetic factors or delayed childbirth, and has wider implications beyond hereditary breast cancer cases. (*) Equal contribution as first authors.
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卡麦角林是小鼠和人类妊娠后乳腺癌预防的新策略
摘要 怀孕后患乳腺癌的预后往往很差,给临床带来了巨大挑战。晚期妊娠的增加趋势加剧了这一风险,凸显了对有效化学预防策略的需求。目前的选择仅限于选择性雌激素受体调节剂、芳香化酶抑制剂或外科手术,但疗效有限且副作用较大。在此,我们报告了卡麦角林(一种多巴胺能激动剂)可降低 Brca1/P53 缺陷小鼠模型中妊娠后患乳腺癌的风险,这对人类乳腺癌的预防具有重要意义。我们的研究表明,在缺乏 Brca1/P53 基因的小鼠中,妊娠后服用单剂量卡贝戈林可显著推迟乳腺癌的发病时间并降低发病率。组织学分析表明,泌乳后内陷在短期内明显加速,其特点是细胞凋亡增加和与离子转运有关的基因表达发生改变。从长期来看,乳腺的组织学变化包括导管成分减少、上皮增殖减少以及作为肿瘤前体的重组 Brca1/P53 靶细胞减少。这些变化可作为乳腺癌易感性降低的指标。此外,RNA 测序确定了与增殖和乳腺分支减少相关的基因表达改变。我们的研究结果强调了一种机制,即卡贝戈林通过增强泌乳后内缩的作用,增强妊娠对乳腺癌的保护作用。值得注意的是,一项针对妇女的回顾性队列研究显示,与对照组相比,接受卡麦角林治疗的妇女妊娠后乳腺癌发病率明显降低。我们的研究强调了加强泌乳后内缩作为乳腺癌预防策略的重要性,并将卡麦角林确定为乳腺癌化学预防中一种前景广阔的低风险选择。这一策略有可能彻底改变乳腺癌的预防方法,尤其是对因遗传因素或延迟生育而导致风险增加的妇女而言,其影响远远超出遗传性乳腺癌病例。(*) 作为第一作者的贡献相同。
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