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表观遗传控制癌症细胞休眠和在激素治疗抵抗中的觉醒。

Epigenetic Control of Cancer Cell Dormancy and Awakening in Endocrine Therapy Resistance.

机构信息

Cancer Computational Biology Group, Vall d'Hebron Institute of Onco-logy, Barcelona, Spain.

Department of Medical Oncology, Vall d'Hebron University Hospital, Barcelona, Spain.

出版信息

Cancer Discov. 2024 May 1;14(5):704-706. doi: 10.1158/2159-8290.CD-24-0282.


DOI:10.1158/2159-8290.CD-24-0282
PMID:38690600
Abstract

Rosano, Sofyali, Dhiman, and colleagues show that epigenetic-related changes occur in endocrine therapy (ET)-induced dormancy in estrogen receptor positive (ER+) breast cancer, as well as in its reawakening. Targeting these epigenetic changes blocks the entrance to dormancy and reduces the persister cancer cell population, enhancing the cytotoxic effects of ET in vitro. See related article by Rosano et al., p. 866 (9).

摘要

罗萨诺、西马利、迪曼等人的研究表明,在雌激素受体阳性(ER+)乳腺癌的内分泌治疗(ET)诱导休眠及其苏醒过程中,会发生与表观遗传相关的变化。针对这些表观遗传变化可以阻止休眠的发生,并减少持久癌细胞的数量,从而增强 ET 在体外的细胞毒性作用。详见罗萨诺等人的相关文章,第 866 页(9)。

相似文献

[1]
Epigenetic Control of Cancer Cell Dormancy and Awakening in Endocrine Therapy Resistance.

Cancer Discov. 2024-5-1

[2]
Endocrine resistance in breast cancer: from cellular signaling pathways to epigenetic mechanisms.

Transcription. 2012

[3]
Epigenetic regulation in estrogen receptor positive breast cancer--role in treatment response.

J Mammary Gland Biol Neoplasia. 2010-1-27

[4]
Epigenetic mechanisms in breast cancer therapy and resistance.

Nat Commun. 2021-3-19

[5]
Tamoxifen resistance and epigenetic modifications in breast cancer cell lines.

Curr Med Chem. 2007

[6]
Reversal of endocrine resistance in breast cancer: interrelationships among 14-3-3ζ, FOXM1, and a gene signature associated with mitosis.

Breast Cancer Res. 2011-6-29

[7]
Activating transcription factor-2 (ATF2) is a key determinant of resistance to endocrine treatment in an in vitro model of breast cancer.

Breast Cancer Res. 2020-11-16

[8]
Candidate methylation sites associated with endocrine therapy resistance in ER+/HER2- breast cancer.

BMC Cancer. 2020-7-19

[9]
Cholesterol biosynthesis pathway as a novel mechanism of resistance to estrogen deprivation in estrogen receptor-positive breast cancer.

Breast Cancer Res. 2016-6-1

[10]
SMAD4 depletion contributes to endocrine resistance by integrating ER and ERBB signaling in HR + HER2- breast cancer.

Cell Death Dis. 2024-6-24

引用本文的文献

[1]
Decoding the adaptive survival mechanisms of breast cancer dormancy.

Oncogene. 2025-8-27

[2]
Epigenetic Therapies in Endocrine-Related Cancers: Past Insights and Clinical Progress.

Cancers (Basel). 2025-7-22

[3]
Bridging the Gap in Breast Cancer Dormancy: Models, Mechanisms, and Translational Challenges.

Pharmaceuticals (Basel). 2025-6-26

[4]
Epigenetic regulation of nuclear receptors: Implications for endocrine-related diseases and therapeutic strategies.

Genes Dis. 2024-12-4

[5]
Tumor dormancy and relapse: understanding the molecular mechanisms of cancer recurrence.

Mil Med Res. 2025-2-11

[6]
Epigenetics-targeted drugs: current paradigms and future challenges.

Signal Transduct Target Ther. 2024-11-26

[7]
Elevated GRHL2 Imparts Plasticity in ER-Positive Breast Cancer Cells.

Cancers (Basel). 2024-8-21

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