Pages
Products
Support
CBpromise

Our promise to you:
Guaranteed product quality, expert customer support.

24x7 CUSTOMER SERVICE
CONTACT US TO ORDER

VcaP Cell Line

General Information
Organism Homo sapiens, human
Cell Line Description VCaP is a human prostate cancer cell line established by K.J. Pienta and colleagues in 1997. The cell line was derived from a 59-year-old Caucasian male with advanced, hormone-refractory prostate cancer; the sample was obtained from a metastatic lesion in the lumbar spine during autopsy. The harvested tissue was initially propagated as a xenograft in SCID mice before being established as an in vitro cell line. VCaP cells exhibit an epithelioid morphology, growing as flat, tightly packed adherent cell islands accompanied by scattered clusters of floating cells. In the field of translational oncology, VCaP is regarded as a highly valuable and pivotal physiological model. It is widely recognized as the only native prostate cancer cell model capable of simultaneously expressing the TMPRSS2-ERG gene fusion and androgen receptor splice variant 7 (AR-V7), making it a cornerstone tool for modeling advanced castration-resistant prostate cancer (CRPC).
Tissue Prostate
Disease Prostate Carcinoma / Castration-Resistant Prostate Cancer (CRPC)
Morphology Epithelial-like; grows in small, tightly formed clusters and flattened clonal islands
Gender Male
Age 59 years
Product Format Frozen
Growth Mode Adherent
Biosafety Level 2 (BSL-2 is standardly enforced; during its historical mouse xenograft passaging, the line acquired an integrated xenotropic murine leukemia virus-related virus, XMRV/Bxv-1, and secretes viral particles)
Applications 1. An indispensable in vitro model for studying the structural basis of oncogenesis driven by the TMPRSS2-ERG chromosomal translocation;
2. Investigating the mechanisms underlying castration resistance, androgen-independent growth, and AR-V7 splice variant signaling;
3. Preclinical validation of next-generation androgen receptor antagonists (e.g., enzalutamide) and targeted therapies;
4. Elucidating the dynamics of organ-specific bone tropism and osteolytic/osteoblastic bone metastasis in prostate cancer;
5. Establishing subcutaneous or orthotopic tumor xenograft models in immunodeficient mice that exhibit slow growth and closely recapitulate clinical pathological features.
Shipped In Dry ice
Storage Temperature −196°C
Characteristics
Tumorigenic Yes; highly tumorigenic in immunocompromised mice, mirroring human metastatic skeletal presentation.
Oncogenic Drivers 1. TMPRSS2-ERG fusion: A hallmark gene fusion associated with prostate cancer.
2. AR-V7 splice variant: Constitutive expression of a truncated androgen receptor that remains active in a ligand-independent manner.
Expression Profile Natively synthesizes copious quantities of Prostate-Specific Antigen (PSA), Prostatic Acid Phosphatase (PAP), Cytokeratin-18, and wild-type Androgen Receptors (AR).
Mycoplasma Test Negative
Culture Conditions and Handling
Subculturing 1. Do not discard the floating cells. These clusters of floating cells contain a significant number of viable cells in the mitotic phase.
2. Collect the spent medium containing the floating cell clusters and transfer it to a sterile conical centrifuge tube. Centrifuge at a low speed (approximately 125 × g) for 5 minutes to pellet the cells.
3. Wash the remaining adherent monolayer cells with sterile PBS (free of Ca2+ and Mg2+).
4. Note on trypsin sensitivity: VCaP cells are highly sensitive to damage caused by trypsin. It is strongly recommended to use Accutase instead of trypsin. Add 1.0 to 2.5 mL of Accutase and incubate at room temperature or 37°C for 8 to 10 minutes until the cells detach. Do not assist detachment by tapping or shaking the culture flask.
5. Resuspend the detached cells in complete medium and combine them with the cell pellet collected from the spent medium.
6. Centrifuge the combined cell suspension at low speed, resuspend in a mixture of media (e.g., 90% fresh medium + 10% sterile-filtered spent medium), and seed into a new culture vessel.
Culture Conditions Atmosphere: Air, 95%; CO2, 5%; Temperature: 37°C
Cryopreservation 90% Complete culture growth medium + 10% DMSO (or 50% Basal medium + 40% FBS + 10% DMSO)

The above is only part of a part of cell line products. If you don't find the cell line you want, Creative Biogene can also provide stable cell line generation service with the best prices and fastest turnaround time for you! Contact us for more information or to request a quote.

* For research use only. Not intended for any clinical use.
Quick Inquiry