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维生素D充足可增强患者来源的前列腺上皮类器官的分化。

Vitamin D sufficiency enhances differentiation of patient-derived prostate epithelial organoids.

作者信息

McCray Tara, Pacheco Julian V, Loitz Candice C, Garcia Jason, Baumann Bethany, Schlicht Michael J, Valyi-Nagy Klara, Abern Michael R, Nonn Larisa

机构信息

Department of Pathology, University of Illinois at Chicago, 840 S Wood Street, Chicago, IL 60612, USA.

University of Illinois Cancer Center, Chicago, IL 60612, USA.

出版信息

iScience. 2021 Jan 5;24(1):101974. doi: 10.1016/j.isci.2020.101974. eCollection 2021 Jan 22.


DOI:10.1016/j.isci.2020.101974
PMID:33458620
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7797919/
Abstract

Vitamin D is an essential steroid hormone that regulates systemic calcium homeostasis and cell fate decisions. The prostate gland is hormonally regulated, requiring steroids for proliferation and differentiation of secretory luminal cells. Vitamin D deficiency is associated with an increased risk of lethal prostate cancer, which exhibits a dedifferentiated pathology, linking vitamin D sufficiency to epithelial differentiation. To determine vitamin D regulation of prostatic epithelial differentiation, patient-derived benign prostate epithelial organoids were grown in vitamin D-deficient or -sufficient conditions. Organoids were assessed by phenotype and single-cell RNA sequencing. Mechanistic validation demonstrated that vitamin D sufficiency promoted organoid growth and accelerated differentiation by inhibiting canonical Wnt activity and suppressing Wnt family member DKK3. Wnt and DKK3 were also reduced by vitamin D in prostate tissue explants by spatial transcriptomics. Wnt dysregulation is a known contributor to aggressive prostate cancer, thus findings further link vitamin D deficiency to lethal disease.

摘要

维生素D是一种重要的类固醇激素,可调节全身钙稳态和细胞命运决定。前列腺受激素调节,分泌性管腔细胞的增殖和分化需要类固醇。维生素D缺乏与致命性前列腺癌风险增加有关,后者表现出去分化病理,将维生素D充足与上皮分化联系起来。为了确定维生素D对前列腺上皮分化的调节作用,将患者来源的良性前列腺上皮类器官在维生素D缺乏或充足的条件下培养。通过表型和单细胞RNA测序对类器官进行评估。机制验证表明,维生素D充足通过抑制经典Wnt活性和抑制Wnt家族成员DKK3促进类器官生长并加速分化。通过空间转录组学研究发现,维生素D还可降低前列腺组织外植体中的Wnt和DKK3。Wnt失调是侵袭性前列腺癌的已知促成因素,因此这些发现进一步将维生素D缺乏与致命性疾病联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/c3234f9e410e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/57bc0f10100c/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/228bc44f7345/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/d7d1a2952d4e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/9edfebfeb7cf/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/d2d61c153f88/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/971a995f8710/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/c3234f9e410e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/57bc0f10100c/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/228bc44f7345/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/d7d1a2952d4e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/9edfebfeb7cf/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/d2d61c153f88/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/971a995f8710/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5f/7797919/c3234f9e410e/gr6.jpg

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引用本文的文献

[1]
Potential role of DKK3 and WIF1 in prostate cancer: bioinformatics and clinical analysis.

Discov Oncol. 2025-8-27

[2]
Multi-task benchmarking of spatially resolved gene expression simulation models.

Genome Biol. 2025-3-17

[3]
Single-Cell Analysis Dissects the Effects of Vitamin D on Genetic Senescence Signatures Across Murine Tissues.

Nutrients. 2025-1-24

[4]
Targeting Androgen, Thyroid Hormone, and Vitamin A and D Receptors to Treat Prostate Cancer.

Int J Mol Sci. 2024-8-26

[5]
Discordant Health Implications and Molecular Mechanisms of Vitamin D in Clinical and Preclinical Studies of Prostate Cancer: A Critical Appraisal of the Literature Data.

Int J Mol Sci. 2024-5-13

[6]
Exploration of vitamin D metabolic activity-related biological effects and corresponding therapeutic targets in prostate cancer.

Nutr Metab (Lond). 2024-4-2

[7]
The complex interplay of modifiable risk factors affecting prostate cancer disparities in African American men.

Nat Rev Urol. 2024-7

[8]
Evaluating spatially variable gene detection methods for spatial transcriptomics data.

Genome Biol. 2024-1-15

[9]
Unveiling novel insights in prostate cancer through single-cell RNA sequencing.

Front Oncol. 2023-9-8

[10]
Preclinical models of prostate cancer - modelling androgen dependency and castration resistance in vitro, ex vivo and in vivo.

Nat Rev Urol. 2023-8

本文引用的文献

[1]
Wnt Signaling Drives Prostate Cancer Bone Metastatic Tropism and Invasion.

Transl Oncol. 2020-4

[2]
Snake Venom Gland Organoids.

Cell. 2020-1-23

[3]
In vitro studies revealed a downregulation of Wnt/β-catenin cascade by active vitamin D and TX 527 analog in a Kaposi's sarcoma cellular model.

Toxicol In Vitro. 2019-12-12

[4]
miR-1303 promotes the proliferation, migration and invasion of prostate cancer cells through regulating the Wnt/β-catenin pathway by targeting DKK3.

Exp Ther Med. 2019-12

[5]
Calcitriol inhibits migration and invasion of renal cell carcinoma cells by suppressing Smad2/3-, STAT3- and β-catenin-mediated epithelial-mesenchymal transition.

Cancer Sci. 2020-1

[6]
Vitamin D-VDR Signaling Inhibits Wnt/β-Catenin-Mediated Melanoma Progression and Promotes Antitumor Immunity.

Cancer Res. 2019-11-5

[7]
Single-cell RNA-Seq analysis identifies a putative epithelial stem cell population in human primary prostate cells in monolayer and organoid culture conditions.

Am J Clin Exp Urol. 2019-6-15

[8]
Association among plasma 1,25(OH) D, ratio of 1,25(OH) D to 25(OH)D, and prostate cancer aggressiveness.

Prostate. 2019-5-11

[9]
Vitamin D Signaling Suppresses Early Prostate Carcinogenesis in TgAPT Mice.

Cancer Prev Res (Phila). 2019-4-26

[10]
High levels of PIWI-interacting RNAs are present in the small RNA landscape of prostate epithelium from vitamin D clinical trial specimens.

Prostate. 2019-3-24

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