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微环境中的白介素-1β通过激活 Wnt 信号促进乳腺癌在骨中的转移定植。

Microenvironmental IL1β promotes breast cancer metastatic colonisation in the bone via activation of Wnt signalling.

机构信息

Breast Biology Group, Manchester Breast Centre, Division of Cancer Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Wilmslow Road, Manchester, M20 4GJ, UK.

Division of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Oxford Road, Manchester, M13 9PT, UK.

出版信息

Nat Commun. 2019 Nov 1;10(1):5016. doi: 10.1038/s41467-019-12807-0.

Abstract

Dissemination of tumour cells to the bone marrow is an early event in breast cancer, however cells may lie dormant for many years before bone metastases develop. Treatment for bone metastases is not curative, therefore new adjuvant therapies which prevent the colonisation of disseminated cells into metastatic lesions are required. There is evidence that cancer stem cells (CSCs) within breast tumours are capable of metastasis, but the mechanism by which these colonise bone is unknown. Here, we establish that bone marrow-derived IL1β stimulates breast cancer cell colonisation in the bone by inducing intracellular NFkB and CREB signalling in breast cancer cells, leading to autocrine Wnt signalling and CSC colony formation. Importantly, we show that inhibition of this pathway prevents both CSC colony formation in the bone environment, and bone metastasis. These findings establish that targeting IL1β-NFKB/CREB-Wnt signalling should be considered for adjuvant therapy to prevent breast cancer bone metastasis.

摘要

肿瘤细胞向骨髓的扩散是乳腺癌的早期事件,然而,在骨转移发展之前,这些细胞可能会潜伏多年。骨转移的治疗并非根治性的,因此需要新的辅助疗法来防止播散细胞定植到转移性病变中。有证据表明,乳腺癌肿瘤中的癌症干细胞(CSCs)能够转移,但这些细胞定植到骨骼中的机制尚不清楚。在这里,我们确定骨髓衍生的 IL1β 通过诱导乳腺癌细胞中的细胞内 NFkB 和 CREB 信号转导,刺激乳腺癌细胞在骨骼中的定植,从而导致自分泌 Wnt 信号转导和 CSC 集落形成。重要的是,我们表明,抑制该途径可防止 CSC 在骨环境中的集落形成和骨转移。这些发现确立了靶向 IL1β-NFKB/CREB-Wnt 信号转导应被考虑用于辅助治疗以预防乳腺癌骨转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4817/6825219/6e5d5f5dc440/41467_2019_12807_Fig1_HTML.jpg

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