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本文引用的文献

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Glioma Stem Cell Niches in Human Glioblastoma Are Periarteriolar.人胶质母细胞瘤中的神经胶质瘤干细胞龛位于血管周围。
J Histochem Cytochem. 2018 May;66(5):349-358. doi: 10.1369/0022155417752676. Epub 2018 Jan 12.
2
Hallmarks of glioblastoma: a systematic review.胶质母细胞瘤的特征:一项系统综述。
ESMO Open. 2017 Feb 22;1(6):e000144. doi: 10.1136/esmoopen-2016-000144. eCollection 2016.
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Extracellular Vesicles As Modulators of Tumor Microenvironment and Disease Progression in Glioma.细胞外囊泡作为胶质瘤肿瘤微环境和疾病进展的调节因子
Front Oncol. 2017 Jul 5;7:144. doi: 10.3389/fonc.2017.00144. eCollection 2017.
4
Molecular and Microenvironmental Determinants of Glioma Stem-Like Cell Survival and Invasion.胶质瘤干细胞样细胞存活和侵袭的分子及微环境决定因素
Front Oncol. 2017 Jun 16;7:120. doi: 10.3389/fonc.2017.00120. eCollection 2017.
5
The novel CXCR4 antagonist, PRX177561, reduces tumor cell proliferation and accelerates cancer stem cell differentiation in glioblastoma preclinical models.新型CXCR4拮抗剂PRX177561在胶质母细胞瘤临床前模型中可降低肿瘤细胞增殖并加速癌症干细胞分化。
Tumour Biol. 2017 Jun;39(6):1010428317695528. doi: 10.1177/1010428317695528.
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DNA Damage in Stem Cells.干细胞中的 DNA 损伤。
Mol Cell. 2017 May 4;66(3):306-319. doi: 10.1016/j.molcel.2017.04.006.
7
Novel therapeutic strategies to target leukemic cells that hijack compartmentalized continuous hematopoietic stem cell niches.针对劫持局部化连续造血干细胞龛的白血病细胞的新型治疗策略。
Biochim Biophys Acta Rev Cancer. 2017 Aug;1868(1):183-198. doi: 10.1016/j.bbcan.2017.03.010. Epub 2017 Mar 28.
8
The brain-penetrating CXCR4 antagonist, PRX177561, increases the antitumor effects of bevacizumab and sunitinib in preclinical models of human glioblastoma.可穿透血脑屏障的CXCR4拮抗剂PRX177561在人胶质母细胞瘤临床前模型中增强了贝伐单抗和舒尼替尼的抗肿瘤作用。
J Hematol Oncol. 2017 Jan 5;10(1):5. doi: 10.1186/s13045-016-0377-8.
9
Cathepsin K cleavage of SDF-1α inhibits its chemotactic activity towards glioblastoma stem-like cells.组织蛋白酶 K 对 SDF-1α 的裂解抑制了其对神经胶质瘤干细胞样细胞的趋化活性。
Biochim Biophys Acta Mol Cell Res. 2017 Mar;1864(3):594-603. doi: 10.1016/j.bbamcr.2016.12.021. Epub 2016 Dec 28.
10
Glioblastoma Stem-Like Cells: Characteristics, Microenvironment, and Therapy.胶质母细胞瘤干细胞样细胞:特征、微环境与治疗
Front Pharmacol. 2016 Dec 7;7:477. doi: 10.3389/fphar.2016.00477. eCollection 2016.

血管周胶质母细胞瘤干细胞龛表达骨髓造血干细胞龛蛋白。

Periarteriolar Glioblastoma Stem Cell Niches Express Bone Marrow Hematopoietic Stem Cell Niche Proteins.

机构信息

Department of Medical Biology, Cancer Center Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.

Department of Genetic Toxicology and Cancer Biology, National Institute of Biology, Ljubljana, Slovenia.

出版信息

J Histochem Cytochem. 2018 Mar;66(3):155-173. doi: 10.1369/0022155417749174. Epub 2018 Jan 3.

DOI:10.1369/0022155417749174
PMID:29297738
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5833177/
Abstract

In glioblastoma, a fraction of malignant cells consists of therapy-resistant glioblastoma stem cells (GSCs) residing in protective niches that recapitulate hematopoietic stem cell (HSC) niches in bone marrow. We have previously shown that HSC niche proteins stromal cell-derived factor-1α (SDF-1α), C-X-C chemokine receptor type 4 (CXCR4), osteopontin (OPN), and cathepsin K (CatK) are expressed in hypoxic GSC niches around arterioles in five human glioblastoma samples. In HSC niches, HSCs are retained by binding of SDF-1α and OPN to their receptors CXCR4 and CD44, respectively. Protease CatK cleaves SDF-1α to release HSCs out of niches. The aim of the present study was to reproduce the immunohistochemical localization of these GSC markers in 16 human glioblastoma samples with the addition of three novel markers. Furthermore, we assessed the type of blood vessels associated with GSC niches. In total, we found seven GSC niches containing CD133-positive and nestin-positive GSCs as a single-cell layer exclusively around the tunica adventitia of 2% of the CD31-positive and SMA-positive arterioles and not around capillaries and venules. Niches expressed SDF-1α, CXCR4, CatK, OPN, CD44, hypoxia-inducible factor-1α, and vascular endothelial growth factor. In conclusion, we show that GSC niches are present around arterioles and express bone marrow HSC niche proteins.

摘要

在胶质母细胞瘤中,一部分恶性细胞由位于保护性龛位中的耐药性胶质母细胞瘤干细胞(GSCs)组成,这些龛位模拟了骨髓中的造血干细胞(HSC)龛位。我们之前已经表明,在 5 个人类胶质母细胞瘤样本的小动脉周围的缺氧 GSC 龛位中表达了 HSC 龛位蛋白基质细胞衍生因子-1α(SDF-1α)、C-X-C 趋化因子受体 4(CXCR4)、骨桥蛋白(OPN)和组织蛋白酶 K(CatK)。在 HSC 龛位中,SDF-1α 通过与 CXCR4 结合,OPN 通过与 CD44 结合,将 HSCs 保留在龛位中。蛋白酶 CatK 可切割 SDF-1α,从而将 HSCs 从龛位中释放出来。本研究的目的是在 16 个人类胶质母细胞瘤样本中重现这些 GSC 标志物的免疫组织化学定位,并添加了三个新的标志物。此外,我们评估了与 GSC 龛位相关的血管类型。总共发现了 7 个 GSC 龛位,其中包含 CD133 阳性和巢蛋白阳性的 GSCs,作为单层细胞,仅存在于 2%的 CD31 阳性和 SMA 阳性小动脉的外膜周围,而不存在于毛细血管和小静脉周围。龛位表达 SDF-1α、CXCR4、CatK、OPN、CD44、缺氧诱导因子-1α 和血管内皮生长因子。总之,我们表明 GSC 龛位存在于小动脉周围,并表达骨髓 HSC 龛位蛋白。