Brain/Nerve Tumor Cells

Brain and nerve tumors originate from diverse cell types within the central and peripheral nervous systems, including glial cells, neurons, and nerve sheath components. These tumors encompass a wide spectrum of diseases, such as gliomas, neuroblastomas, meningiomas, and schwannomas, each with distinct biological behaviors and levels of malignancy.

Our brain/nerve tumor cell line collection provides physiologically relevant in vitro models for studying tumor heterogeneity, neural lineage differentiation, and mechanisms of tumor progression, as well as for evaluating therapeutic strategies targeting cancers of the nervous system.

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Key Features & Expertise

Our brain and nerve tumor cell lines are designed to support advanced neuro-oncology research

Broad Representation of Nervous System Tumors

  • Includes glioma, neuroblastoma, meningioma, and schwannoma models
  • Covers both central and peripheral nervous system tumor types
  • Supports studies across benign and malignant disease contexts

Reflective of Cellular and Molecular Heterogeneity

  • Models derived from distinct neural lineages, including glial and neural crest origins
  • Capture variability in differentiation status and tumor aggressiveness
  • Applicable to studies of tumor evolution, signaling pathways, and resistance mechanisms

Validated Quality for Research Applications

  • STR-authenticated to ensure cell line identity
  • Mycoplasma-free and rigorously quality controlled
  • Reliable performance in drug screening and mechanistic studies

FAQ

What types of brain and nerve tumor cell lines are included?

This collection includes a variety of tumor models such as glioma (including astrocytoma and glioblastoma), neuroblastoma, meningioma, and schwannoma cell lines, representing both central and peripheral nervous system tumors.

How do I select the right model for my research?

Model selection depends on your research goals. Key considerations include:

  • Tumor origin (central vs. peripheral nervous system)
  • Cell lineage (glial vs. neuronal vs. neural crest-derived)
  • Malignancy grade and growth characteristics
  • Relevance to your therapeutic or mechanistic study

What makes brain and nerve tumor models challenging to study?

These tumors are highly heterogeneous, with diverse genetic and cellular features. Their complex microenvironment and lineage diversity can make experimental interpretation more challenging compared to other tumor types.

Can these cell lines be used for drug discovery?

Yes, brain and nerve tumor cell lines are widely used in drug discovery and screening, enabling evaluation of therapeutic efficacy, mechanism of action, and subtype-specific responses in neuro-oncology research.

Do these models reflect tumor heterogeneity?

While individual cell lines represent specific tumor characteristics, using a panel of models allows researchers to capture the diversity of nervous system tumors, including differences in lineage, differentiation state, and aggressiveness.

Is molecular characterization data available?

For many cell lines, relevant characterization data such as mutation profiles and pathway information are available, supporting informed model selection and experimental design.

How should these cell lines be stored and handled?

Cell lines are typically supplied as cryopreserved vials or shipped on dry ice. Upon receipt, they should be stored in liquid nitrogen and handled using standard cell culture protocols to ensure optimal viability and consistency.

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NGP
NGP

Description: Established 1974 from lung metastases obtained at post mortem from a 2 1/2-year-old boy with ...

Cat#: CSC-C2562 INQUIRY

Description: Established from the adrenal tumor tissue resected after treatment from a 20-month-old boy of ...

Cat#: CSC-C3438 INQUIRY

Description: Established in 2011 from a metastasized group 3 medulloblastoma in the cerebellum of a 3-year-old ...

Cat#: CSC-C6241X INQUIRY

Description: Human cell line derived from malignant peripheral nerve sheath tumor (MPNST).

Cat#: CSC-C6318J INQUIRY

Description: Human cell line derived from Hodgkin's lymphoma.

Cat#: CSC-C6331J INQUIRY

Description: Human neuroblastoma cell line.

Cat#: CSC-C6339J INQUIRY

Description: Human cell line derived from neuroblastoma. Dibuty-cAMP (1 mM) induces differentiation.

Cat#: CSC-C6340J INQUIRY

Description: Human cell line derived from astrocytoma developed in a patient with NF-1 (neurofibromatosis type 1)

Cat#: CSC-C6370J INQUIRY

Description: Human brain derived lymphoma. Epstein-Barr virus positive.

Cat#: CSC-C6448J INQUIRY

Description: Human glioma separated from gliosarcoma.

Cat#: CSC-C6455J INQUIRY

Description: Subline of GOTO. Protein-free medium adapted. Cell growth is slow.

Cat#: CSC-C6459J INQUIRY

Description: Human malignant meningioma.

Cat#: CSC-C6466J INQUIRY
NB9
NB9

Description: Neuroblastoma. N-myc gene amplification.

Cat#: CSC-C6501J INQUIRY

Description: Neuroblastoma. N-myc gene amplification.

Cat#: CSC-C6502J INQUIRY

Description: Neuroblastoma. N-myc gene amplification.

Cat#: CSC-C6503J INQUIRY

Description: Subline of U-251 MG with epithelial morphology.

Cat#: CSC-C6634J INQUIRY
TGW
TGW

Description: neuroblastoma, adrenal gland

Cat#: CSC-C6646J INQUIRY

Description: Human cell line with primitive neuroectodermal tumor (Askin's tumor).

Cat#: CSC-C6649J INQUIRY

For research use only. Not for any other purpose.