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乳腺癌中细胞周期、迁移及干细胞样活性的协调作用

Co-ordination of cell cycle, migration and stem cell-like activity in breast cancer.

作者信息

Lamb Rebecca, Lisanti Michael P, Clarke Robert B, Landberg Göran

机构信息

Breakthrough Breast Cancer Unit , Institute of Cancer Sciences, Paterson Institute for Cancer Research, University of Manchester, Wilmslow Road, Manchester, UK.

Breakthrough Breast Cancer Unit , Institute of Cancer Sciences, Paterson Institute for Cancer Research, University of Manchester, Wilmslow Road, Manchester, UK. Center for Molecular Pathology, Department of Laboratory Medicine, Lund university, Skåne University Hospital, Malmö, Sweden. Sahlgrenska Cancer Center, University of Gothenburg, Sweden.

出版信息

Oncotarget. 2014 Sep 15;5(17):7833-42. doi: 10.18632/oncotarget.2312.

Abstract

Migration, proliferation and stem cell-like activity are all key cellular characteristics which aid the formation and progression of breast cancer, in addition to involvement in treatment resistance. Many current therapies aim to target tumour proliferation, and although successful, mortality rates in breast cancer remain significant. Our main objectives were to investigate the relationship between proliferation, migration and stem cell-like activity in breast cancer. We used a panel of cell lines and primary human breast cancer samples to assess the relationship between migration, proliferation and stem cells. We performed live cell sorting according to cell cycle (Hoechst-33324) and in combination with stem-cell markers (CD44/CD24/ESA) followed by assessment of migration and stem cell activity (mammosphere formation). We identified an inverse relationship between proliferation and migration/stem cell-like activity. G0/1 cells showed increased migration and mammosphere formation. Furthermore we identified a subpopulation of low proliferative stem-like cells (CD44+/24lo/ESA+) with increased migration and mammosphere formation that are specifically inhibited by Dickkopf 1 (DKK1) and Dibenzazepine (DBZ) known stem-cell inhibitors. These data show the co-ordination of migration, proliferation and stem cell activity in breast cancer, and has identified a sub-population of stem-like cells, greatly adding to our understanding of the complex nature of stem cell biology.

摘要

迁移、增殖和干细胞样活性都是关键的细胞特征,这些特征不仅有助于乳腺癌的形成和进展,还与治疗耐药性有关。目前许多疗法旨在靶向肿瘤增殖,尽管取得了成功,但乳腺癌的死亡率仍然很高。我们的主要目标是研究乳腺癌中增殖、迁移和干细胞样活性之间的关系。我们使用了一组细胞系和原发性人类乳腺癌样本,以评估迁移、增殖和干细胞之间的关系。我们根据细胞周期(Hoechst-33324)并结合干细胞标志物(CD44/CD24/ESA)进行活细胞分选,随后评估迁移和干细胞活性(乳腺球形成)。我们发现增殖与迁移/干细胞样活性之间呈负相关。G0/1期细胞显示出迁移和乳腺球形成增加。此外,我们鉴定出一个低增殖干细胞样亚群(CD44+/24lo/ESA+),其迁移和乳腺球形成增加,而已知的干细胞抑制剂Dickkopf 1(DKK1)和二苯并氮杂卓(DBZ)可特异性抑制该亚群。这些数据表明了乳腺癌中迁移、增殖和干细胞活性之间的协同作用,并鉴定出了一个干细胞样亚群,极大地增进了我们对干细胞生物学复杂本质的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd04/4202164/8a8c1dc82d91/oncotarget-05-7833-g001.jpg

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