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Tumor Cell Lines

LNCaP, clone FGC

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LNCaP clone FGC was isolated in 1977 by J.S. Horoszewicz, et al., From a needle aspiration biopsy of the left supraclavicular lymph node of a 50-year-old Caucasian male (blood type B+) with confirmed diagnosis of metastatic prostate carcinoma.
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Product Code

LNCaP-Clone-FGC; LNCaP.FGC; LNCaP-FGC; LNCaP FGC; LNCAPCLONEFGC

Species

Human

Cat.No

ABC-TC0599

Product Category Tumor Cell Lines
Size/Quantity

1 vial

Cell Type

Epithelial

Shipping Info

Dry Ice

Growth Conditions

37 ℃, 5% CO2

Biosafety Level

1

Storage

Liquid Nitrogen

Product Type

Human Prostate Cancer Cell Lines

Description

LNCaP, clone FGCThe LNCaP cell line was established in 1977 from a metastatic lesion in the left supraclavicular lymph node of a 50-year-old Caucasian male with prostate carcinoma. These cells grow in aggregates or as single cells, with a weak attachment to the substrate and a tendency to rapidly acidify the growth medium. LNCaP cells have a high affinity for androgen receptors and respond to hormonal stimulation. Unlike other cell lines, they do not form a uniform monolayer, instead growing in clusters that require dissociation for subculture. They are tumorigenic in immunodeficient mice and are frequently used for prostate cancer research. LNCaP cells are free from mycoplasma, bacteria, yeast, and fungi. These cells serve as an excellent in vitro model for studying prostate cancer, androgen receptor signaling, and drug resistance.

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Citation

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Application

  • The LNCaP cell line can be used to develop the CDX-type LNCaP mouse model. This model is valuable for studying androgen sensitivity, as LNCaP cells possess a mutated androgen receptor (AR T877A). The LNCaP xenograft model serves as an androgen-dependent system and is utilized for evaluating various treatment modalities targeting the androgen receptor, such as AR-targeting oligos or bicalutamide. This model provides a platform to study how well these treatments work and how they function in the context of androgen-dependent prostate cancer.

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