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间质干细胞在调节乳腺癌微环境中的作用。

The Role of Mesenchymal Stem Cells in Modulating the Breast Cancer Microenvironment.

机构信息

Department of Surgical Oncology, Central Hospital Affiliated to Shandong First Medical University, Jinan, China.

出版信息

Cell Transplant. 2023 Jan-Dec;32:9636897231220073. doi: 10.1177/09636897231220073.


DOI:10.1177/09636897231220073
PMID:38135917
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10748553/
Abstract

The role of mesenchymal stem cells (MSCs) in the breast tumor microenvironment (TME) is significant and multifaceted. MSCs are recruited to breast tumor sites through molecular signals released by tumor sites. Once in the TME, MSCs undergo polarization and interact with various cell populations, including immune cells, cancer-associated fibroblasts (CAFs), cancer stem cells (CSCs), and breast cancer cells. In most cases, MSCs play roles in breast cancer therapeutic resistance, but there is also evidence that indicates their abilities to sensitize cancer cells to chemotherapy and radiotherapy. MSCs possess inherent regenerative and homing properties, making them attractive candidates for cell-based therapies. Therefore, MSCs can be engineered to express therapeutic molecules or deliver anti-cancer agents directly to tumor sites. Unraveling the intricate relationship between MSCs and the breast TME has the potential to uncover novel therapeutic targets and advance our understanding of breast cancer biology.

摘要

间充质干细胞(MSCs)在乳腺肿瘤微环境(TME)中的作用是显著的且多方面的。MSCs 通过肿瘤部位释放的分子信号被招募到乳腺肿瘤部位。一旦进入 TME,MSCs 就会发生极化,并与各种细胞群体相互作用,包括免疫细胞、癌相关成纤维细胞(CAFs)、癌症干细胞(CSCs)和乳腺癌细胞。在大多数情况下,MSCs 发挥着乳腺癌治疗耐药的作用,但也有证据表明它们能够使癌细胞对化疗和放疗敏感。MSCs 具有内在的再生和归巢特性,使其成为细胞治疗的有吸引力的候选者。因此,可以对 MSCs 进行工程改造,使其表达治疗分子或直接将抗癌剂递送到肿瘤部位。阐明 MSCs 与乳腺 TME 之间的复杂关系有潜力揭示新的治疗靶点,并深入了解乳腺癌生物学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b2/10748553/5fb2b9fb09ca/10.1177_09636897231220073-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b2/10748553/b328772228d1/10.1177_09636897231220073-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b2/10748553/b8b91e0cff78/10.1177_09636897231220073-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b2/10748553/5fb2b9fb09ca/10.1177_09636897231220073-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b2/10748553/b328772228d1/10.1177_09636897231220073-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b2/10748553/b8b91e0cff78/10.1177_09636897231220073-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b2/10748553/5fb2b9fb09ca/10.1177_09636897231220073-fig3.jpg

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The Role of Mesenchymal Stem Cells in Modulating the Breast Cancer Microenvironment.

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[10]
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本文引用的文献

[1]
The Dose-Related Efficacy of Human Placenta-Derived Mesenchymal Stem Cell Transplantation on Antioxidant Effects in a Rat Model with Ovariectomy.

Antioxidants (Basel). 2023-8-7

[2]
Cancer-associated fibroblasts facilitate breast cancer progression through exosomal circTBPL1-mediated intercellular communication.

Cell Death Dis. 2023-7-26

[3]
Mitochondria Transfer from Mesenchymal Stem Cells Confers Chemoresistance to Glioblastoma Stem Cells through Metabolic Rewiring.

Cancer Res Commun. 2023-6

[4]
Breast cancer cell mesenchymal transition and metastasis directed by DAP5/eIF3d-mediated selective mRNA translation.

Cell Rep. 2023-6-27

[5]
Resistance to mesenchymal reprogramming sustains clonal propagation in metastatic breast cancer.

Cell Rep. 2023-6-27

[6]
Advances in Radiotherapy for Breast Cancer.

Surg Oncol Clin N Am. 2023-7

[7]
Extracellular Lactic Acidosis of the Tumor Microenvironment Drives Adipocyte-to-Myofibroblast Transition Fueling the Generation of Cancer-Associated Fibroblasts.

Cells. 2023-3-20

[8]
Mesenchymal stem cell suppresses the efficacy of CAR-T toward killing lymphoma cells by modulating the microenvironment through stanniocalcin-1.

Elife. 2023-2-13

[9]
Breast Cancer: Risk Assessment, Screening, and Primary Prevention.

Med Clin North Am. 2023-3

[10]
Involvement of protumor macrophages in breast cancer progression and characterization of macrophage phenotypes.

Cancer Sci. 2023-6

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