scispace - formally typeset
Open AccessJournal ArticleDOI

Neurofibromas in NF1: Schwann Cell Origin and Role of Tumor Environment

TLDR
Through use of a conditional (cre/lox) allele, it is shown that loss of NF1 in the Schwann cell lineage is sufficient to generate tumors and the requirement for a permissive haploinsufficient environment to allow tumorigenesis may have therapeutic implications for NF1 and other familial cancers.
Abstract
Neurofibromatosis type 1 (NF1) is one of the most prevalent dominantly inherited genetic diseases of the nervous system. NF1 encodes a tumor suppressor whose functional loss results in the development of benign neurofibromas that can progress to malignancy. Neurofibromas are complex tumors composed of axonal processes, Schwann cells, fibroblasts, perineurial cells, and mast cells. Through use of a conditional (cre/lox) allele, we show that loss of NF1 in the Schwann cell lineage is sufficient to generate tumors. In addition, complete NF1-mediated tumorigenicity requires both a loss of NF1 in cells destined to become neoplastic as well as heterozygosity in non-neoplastic cells. The requirement for a permissive haploinsufficient environment to allow tumorigenesis may have therapeutic implications for NF1 and other familial cancers.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Stem Cells and Niches: Mechanisms That Promote Stem Cell Maintenance throughout Life

TL;DR: Niches are local tissue microenvironments that maintain and regulate stem cells that are key to the regulation of homeostasis and likely contribute to aging and tumorigenesis when altered during adulthood.
Journal ArticleDOI

Friends or foes - bipolar effects of the tumour stroma in cancer.

TL;DR: The restricted view of tumour progression as a multistep process defined by the accumulation of mutations in cancer cells has largely ignored the substantial contribution of the tumour microenvironment to malignancy.
Journal ArticleDOI

Hyperactive Ras in developmental disorders and cancer.

TL;DR: The implications of germline mutations in the Ras–Raf–MEK–ERK pathway for understanding normal developmental processes and cancer pathogenesis are discussed.
References
More filters
Journal ArticleDOI

The hallmarks of cancer.

TL;DR: This work has been supported by the Department of the Army and the National Institutes of Health, and the author acknowledges the support and encouragement of the National Cancer Institute.
Book

Pathology and genetics of tumours of the nervous system.

TL;DR: Tumours of the haemopoietic system Malignant lymphomas Histiocytic tumours, Familial tumour syndromes, and metastatic tumours ofThe CNS.
Journal ArticleDOI

MMP-9 supplied by bone marrow-derived cells contributes to skin carcinogenesis

TL;DR: The matrix metalloproteinase MMP-9/gelatinase B is upregulated in angiogenic dysplasias and invasive cancers of the epidermis in a mouse model of multi-stage tumorigenesis elicited by HPV16 oncogenes, suggesting inflammatory cells can be coconspirators in carcinogenesis.
Journal ArticleDOI

Neurofibromatosis : phenotype, natural history, and pathogenesis

TL;DR: NF1: historical background and introduction clinical and epidemiologic features evaluation and management genetics molecular biology and pathogenesis neurofibromas and malignanat peripheral nerve sheath tumours cognitive function and academic performance.
Journal ArticleDOI

Krox-20 controls myelination in the peripheral nervous system.

TL;DR: It is demonstrated here that Krox-20 is also activated in Schwann cells before the onset of myelination and that its disruption blocks Schwann Cells at an early stage in their differentiation, thus preventing myelinations in the peripheral nervous system.
Related Papers (5)