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1型神经纤维瘤病患者恶性外周神经鞘膜瘤来源的肿瘤细胞的遗传和表型特征

Genetic and phenotypic characterization of tumor cells derived from malignant peripheral nerve sheath tumors of neurofibromatosis type 1 patients.

作者信息

Frahm Silke, Mautner Victor-F, Brems Hilde, Legius Eric, Debiec-Rychter Maria, Friedrich Reinhard E, Knöfel Wolfram T, Peiper Matthias, Kluwe Lan

机构信息

Laboratory of Brain Tumor Biology, Department of Neurosurgery, University Hospital Eppendorf, Hamburg, Germany.

出版信息

Neurobiol Dis. 2004 Jun;16(1):85-91. doi: 10.1016/j.nbd.2004.01.006.


DOI:10.1016/j.nbd.2004.01.006
PMID:15207265
Abstract

Neurofibromatosis type 1 (NF1) patients have an 8-13% lifetime risk of developing malignant peripheral nerve sheath tumors (MPNST) which have a very poor prognosis. In this study, cells from eight MPNSTs (six primary and two recurrences) of six clinically and genetically well-characterized NF1 patients were taken into culture. Tracing of loss of heterozygosity (LOH) of the NF1, p53, and p16 gene regions or of abnormal karyotypes enabled identification of tumor cells from five MPNSTs. In two other MPNST-derived cell cultures, LOH of the relevant regions in the original tumors could not be detected, indicating that the obtained cells were nonneoplastic cells. Cells from most MPNSTs grew only under standard culture conditions but not under conditions optimized for Schwann cells. These cells were S100-negative and did not exhibit spindle shape which is a characteristic of Schwann cells. Drastically increased proliferation rates were found for most of the MPNST cells in comparison to Schwann cells derived from benign neurofibromas. Our study demonstrates that genetic analysis is effective and essential for verification of MPNST tumor cells in culture. These verified MPNST cells are valuable for further investigations of the biology and pathogenesis of this malignancy as well as for in vitro pharmacologic studies essential for the development of new therapies.

摘要

1型神经纤维瘤病(NF1)患者一生中患恶性外周神经鞘瘤(MPNST)的风险为8%-13%,而MPNST的预后非常差。在本研究中,取自6例临床和基因特征明确的NF1患者的8个MPNST(6个原发性和2个复发性)的细胞被用于培养。通过追踪NF1、p53和p16基因区域的杂合性缺失(LOH)或异常核型,能够鉴定出5个MPNST的肿瘤细胞。在另外两种源自MPNST的细胞培养物中,未检测到原始肿瘤中相关区域的LOH,这表明所获得的细胞是非肿瘤细胞。大多数MPNST的细胞仅在标准培养条件下生长,而在为雪旺细胞优化的条件下则不能生长。这些细胞S100阴性,不呈现雪旺细胞特有的纺锤形。与源自良性神经纤维瘤的雪旺细胞相比,大多数MPNST细胞的增殖率显著增加。我们的研究表明,基因分析对于验证培养中的MPNST肿瘤细胞是有效且必不可少的。这些经过验证的MPNST细胞对于进一步研究这种恶性肿瘤的生物学和发病机制以及对于开发新疗法必不可少的体外药理学研究具有重要价值。

相似文献

[1]
Genetic and phenotypic characterization of tumor cells derived from malignant peripheral nerve sheath tumors of neurofibromatosis type 1 patients.

Neurobiol Dis. 2004-6

[2]
Molecular characterization of permanent cell lines from primary, metastatic and recurrent malignant peripheral nerve sheath tumors (MPNST) with underlying neurofibromatosis-1.

Anticancer Res. 2009-4

[3]
Expression of insulin-like growth-factor-1 receptor (IGF-1R) in peripheral nerve sheath tumors in neurofibromatosis type 1.

Anticancer Res. 2007

[4]
NF1 deficiency causes Bcl-xL upregulation in Schwann cells derived from neurofibromatosis type 1-associated malignant peripheral nerve sheath tumors.

Int J Oncol. 2012-12-24

[5]
Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors.

Genes Chromosomes Cancer. 2011-8-24

[6]
Culture of cytogenetically abnormal schwann cells from benign and malignant NF1 tumors.

Genes Chromosomes Cancer. 2000-2

[7]
Molecular profiling of malignant peripheral nerve sheath tumors associated with neurofibromatosis type 1, based on large-scale real-time RT-PCR.

Mol Cancer. 2004-7-15

[8]
Malignant peripheral nerve sheath tumors (MPNST) in neurofibromatosis type 1 (NF1): diagnostic findings on magnetic resonance images and mutation analysis of the NF1 gene.

Anticancer Res. 2005

[9]
Frequent genomic imbalances in chromosomes 17, 19, and 22q in peripheral nerve sheath tumours detected by comparative genomic hybridization analysis.

J Pathol. 2002-5

[10]
The angiogenic factor midkine is aberrantly expressed in NF1-deficient Schwann cells and is a mitogen for neurofibroma-derived cells.

Oncogene. 2001-1-4

引用本文的文献

[1]
Triple Combination of MEK, BET, and CDK Inhibitors Significantly Reduces Human Malignant Peripheral Nerve Sheath Tumors in Mouse Models.

Clin Cancer Res. 2025-3-3

[2]
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Cancer Genomics Proteomics. 2025

[3]
NF2 with NF1 Features a Unique Overlap.

Indian J Otolaryngol Head Neck Surg. 2024-12

[4]
Silver Nanoparticles Selectively Treat Neurofibromatosis Type 1-Associated Plexiform Neurofibroma Cells at Doses That Do Not Affect Patient-Matched Schwann Cells.

Pharmaceutics. 2024-3-7

[5]
Multiplatform molecular profiling uncovers two subgroups of malignant peripheral nerve sheath tumors with distinct therapeutic vulnerabilities.

Nat Commun. 2023-5-10

[6]
Deep genomic analysis of malignant peripheral nerve sheath tumor cell lines challenges current malignant peripheral nerve sheath tumor diagnosis.

iScience. 2023-1-31

[7]
Silver Nanoparticles Selectively Treat Neurofibromatosis Type 1-Associated Malignant Peripheral Nerve Sheath Tumors in a Neurofibromin-Dependent Manner.

J Pers Med. 2022-6-30

[8]
A High-Throughput Screening Platform Identifies Novel Combination Treatments for Malignant Peripheral Nerve Sheath Tumors.

Mol Cancer Ther. 2022-7-5

[9]
Optimizing Conditions for Spheroid Formation of Dental Pulp Cells in Cell Culture.

In Vivo. 2021

[10]
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Oncol Lett. 2021-6

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