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Bone marrow NG2/Nestin mesenchymal stem cells drive DTC dormancy TGFβ2.骨髓NG2/巢蛋白间充质干细胞通过转化生长因子β2驱动甲状腺微小癌休眠。
Nat Cancer. 2021 Mar;2(3):327-339. doi: 10.1038/s43018-021-00179-8. Epub 2021 Mar 11.
2
The current paradigm and challenges ahead for the dormancy of disseminated tumor cells.播散肿瘤细胞休眠的当前范式和面临的挑战。
Nat Cancer. 2020 Jul;1(7):672-680. doi: 10.1038/s43018-020-0088-5. Epub 2020 Jul 6.
3
Cancer progression and the invisible phase of metastatic colonization.癌症进展与转移性定植的隐匿阶段。
Nat Rev Cancer. 2020 Nov;20(11):681-694. doi: 10.1038/s41568-020-00300-6. Epub 2020 Oct 6.
4
The dormant cancer cell life cycle.休眠癌细胞的生命周期。
Nat Rev Cancer. 2020 Jul;20(7):398-411. doi: 10.1038/s41568-020-0263-0. Epub 2020 Jun 2.
5
Cancer Cell Dormancy in Metastasis.肿瘤细胞休眠与转移
Cold Spring Harb Perspect Med. 2020 Apr 1;10(4):a037556. doi: 10.1101/cshperspect.a037556.
6
Targeting the perivascular niche sensitizes disseminated tumour cells to chemotherapy.针对血管周围基质细胞使播散的肿瘤细胞对化疗更敏感。
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NR2F1 stratifies dormant disseminated tumor cells in breast cancer patients.NR2F1 使乳腺癌患者休眠性播散肿瘤细胞发生分群。
Breast Cancer Res. 2018 Oct 16;20(1):120. doi: 10.1186/s13058-018-1049-0.
8
Tumor cell dormancy: an NCI workshop report.肿瘤细胞休眠:美国国立癌症研究所研讨会报告
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将癌症休眠的科学转化为临床实践。

Translating the Science of Cancer Dormancy to the Clinic.

机构信息

Division of Hematology and Medical Oncology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

Department of Otolaryngology, Icahn School of Medicine at Mount Sinai, New York, New York.

出版信息

Cancer Res. 2021 Sep 15;81(18):4673-4675. doi: 10.1158/0008-5472.CAN-21-1407. Epub 2021 Aug 24.

DOI:10.1158/0008-5472.CAN-21-1407
PMID:34429327
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8562555/
Abstract

The paradigm of metastasis has been significantly remodeled by the incorporation of cancer dormancy as a mechanism to explain long-term remission intervals followed by relapse. There is overall consensus on the potential impact of better understanding dormancy. Key cancer-cell autonomous and microenvironmental mechanisms might explain this biology and, in turn, the timing of metastasis. However, the approach and feasibility to apply this biology to clinical trials has been controversial. The discussion here provides insight into how these controversies are being resolved by the development of active clinical trials, thus bringing to reality opportunities to target cancer dormancy.

摘要

转移的范式已经通过将癌症休眠纳入其中进行了重大重塑,作为解释长期缓解期后复发的一种机制。人们普遍认为更好地理解休眠具有潜在影响。关键的癌细胞自主和微环境机制可能解释这种生物学,进而解释转移的时间。然而,将这种生物学应用于临床试验的方法和可行性一直存在争议。本文讨论了通过开展积极的临床试验如何解决这些争议,从而为靶向癌症休眠带来现实的机会。