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乳腺癌发生过程中的细胞命运决定

Cell Fate Decisions During Breast Cancer Development.

作者信息

Gross Kayla, Wronski Ania, Skibinski Adam, Phillips Sarah, Kuperwasser Charlotte

机构信息

Department of Developmental, Molecular and Chemical Biology, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, 136 Harrison Ave., Boston, MA 02111, USA; Raymond and Beverly Sackler Convergence Laboratory, Tufts University School of Medicine, 145 Harrison Ave., Boston, MA 02111, USA; Molecular Oncology Research Institute, Tufts Medical Center, 800 Washington St., Boston, MA 02111, USA.

Department of Developmental, Molecular and Chemical Biology, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, 136 Harrison Ave., Boston, MA 02111, USA; Molecular Oncology Research Institute, Tufts Medical Center, 800 Washington St., Boston, MA 02111, USA.

出版信息

J Dev Biol. 2016 Mar 1;4(1):4. doi: 10.3390/jdb4010004. Epub 2016 Jan 22.

DOI:10.3390/jdb4010004
PMID:27110512
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4840277/
Abstract

During the formation of breast cancer, many genes become altered as cells evolve progressively from normal to a pre-malignant to a malignant state of growth. How mutations in genes lead to specific subtypes of human breast cancer is only partially understood. Here we review how initial genetic or epigenetic alterations within mammary epithelial cells (MECs) can alter cell fate decisions and put pre-malignant cells on a path towards cancer development with specific phenotypes. Understanding the early stages of breast cancer initiation and progression and how normal developmental processes are hijacked during transformation has significant implications for improving early detection and prevention of breast cancer. In addition, insights gleaned from this understanding may also be important for developing subtype-specific treatment options.

摘要

在乳腺癌形成过程中,随着细胞从正常状态逐渐演变为癌前状态再到恶性生长状态,许多基因会发生改变。基因中的突变如何导致人类乳腺癌的特定亚型,目前仅得到部分理解。在此,我们综述乳腺上皮细胞(MECs)内最初的基因或表观遗传改变如何能够改变细胞命运决定,并使癌前细胞走上具有特定表型的癌症发展道路。了解乳腺癌起始和进展的早期阶段,以及在转化过程中正常发育过程是如何被劫持的,对于改善乳腺癌的早期检测和预防具有重要意义。此外,从这一理解中获得的见解对于开发亚型特异性治疗方案可能也很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4dd/5831812/f173ea9ede0e/jdb-04-00004-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4dd/5831812/f173ea9ede0e/jdb-04-00004-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4dd/5831812/f173ea9ede0e/jdb-04-00004-g001.jpg

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本文引用的文献

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A Progesterone-CXCR4 Axis Controls Mammary Progenitor Cell Fate in the Adult Gland.孕酮-CXCR4轴调控成年乳腺中乳腺祖细胞的命运。
Stem Cell Reports. 2015 Mar 10;4(3):313-322. doi: 10.1016/j.stemcr.2015.01.011. Epub 2015 Feb 19.
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PIK3CA(H1047R) induces multipotency and multi-lineage mammary tumours.PIK3CA(H1047R) 诱导多能性和多谱系乳腺肿瘤。
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A Long-Lived Luminal Subpopulation Enriched with Alveolar Progenitors Serves as Cellular Origin of Heterogeneous Mammary Tumors.
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Myoepithelial progenitors as founder cells of hyperplastic human breast lesions upon PIK3CA transformation.PIK3CA 转化后增生性人类乳腺病变的肌上皮祖细胞作为起始细胞。
Commun Biol. 2022 Mar 10;5(1):219. doi: 10.1038/s42003-022-03161-x.
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Deletion of in the mouse mammary gland results in abnormal accumulation of luminal progenitor cells: a link between reproductive factors and ER-/TNBC breast cancer?小鼠乳腺中[具体基因]的缺失导致管腔祖细胞异常积累:生殖因素与雌激素受体阴性/三阴性乳腺癌之间的联系?
Am J Cancer Res. 2021 Jun 15;11(6):3263-3270. eCollection 2021.
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Highly metastatic claudin-low mammary cancers can originate from luminal epithelial cells.高转移性 Claudin-low 型乳腺癌可起源于腔上皮细胞。
Nat Commun. 2021 Jun 18;12(1):3742. doi: 10.1038/s41467-021-23957-5.
7
Relationships between Breast Feeding and Breast Cancer Subtypes: Lessons Learned from Studies in Humans and in Mice.母乳喂养与乳腺癌亚型的关系:来自人类和小鼠研究的经验教训。
Cancer Res. 2020 Nov 15;80(22):4871-4877. doi: 10.1158/0008-5472.CAN-20-0077. Epub 2020 Aug 14.
8
FOXA1 Protein Expression in ER and ER Breast Cancer in Relation to Parity and Breastfeeding in Black and White Women.FOXA1 蛋白在黑人与白人妇女的 ER 和 ER 阳性乳腺癌中与生育和哺乳的关系。
Cancer Epidemiol Biomarkers Prev. 2020 Feb;29(2):379-385. doi: 10.1158/1055-9965.EPI-19-0787. Epub 2019 Dec 23.
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G3 (Bethesda). 2020 Feb 6;10(2):863-874. doi: 10.1534/g3.119.400850.
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富含肺泡祖细胞的长寿命腔细胞亚群可作为异质性乳腺肿瘤的细胞起源。
Stem Cell Reports. 2015 Jul 14;5(1):60-74. doi: 10.1016/j.stemcr.2015.05.014. Epub 2015 Jun 25.
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