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NCI-H1581
Tissue
Lung
Disease
Large cell carcinoma
Synonyms
H1581, H-1581, NCIH1581

Documents

NCI-H1581

Cell line · Product number 305598

The NCI-H1581 cell line is a human non-small cell lung cancer (NSCLC) model classified as large-cell carcinoma. This cell line is characterized by the amp...

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Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description

The NCI-H1581 cell line is a human non-small cell lung cancer (NSCLC) model classified as large-cell carcinoma. This cell line is characterized by the amplification of the fibroblast growth factor receptor 1 (FGFR1) gene, which plays a critical role in oncogenic signaling pathways, including RAS/RAF/MAPK and PI3K/AKT. FGFR1 amplification and the resultant overexpression make NCI-H1581 a suitable model for studying FGFR-targeted therapies in lung cancer. These cells exhibit high sensitivity to FGFR inhibitors like CPL304110 and AZD4547, which have been shown to significantly reduce proliferation and induce apoptosis in both in vitro and xenograft models.

NCI-H1581 has been extensively utilized to explore resistance mechanisms to FGFR inhibitors. Resistance can emerge through secondary mutations, incomplete pathway inhibition, or activation of alternative signaling routes. Notably, overactivation of the p38 MAPK and AKT pathways has been implicated in acquired resistance to FGFR inhibition in this cell line. Studies show that combining FGFR inhibitors with p38 or AKT pathway inhibitors can restore sensitivity, providing insights into potential combination therapies for FGFR-dependent cancers.

Beyond FGFR research, NCI-H1581 serves as a model to investigate the interplay of oncogenic signaling pathways in large-cell carcinoma. It supports applications in drug discovery, mechanistic studies, and preclinical validation of targeted therapies. The cell line’s genetic and molecular attributes, along with its robust response to specific inhibitors, make it a valuable resource for advancing therapeutic strategies against FGFR1-amplified NSCLC.

Tissue
Lung
Disease
Large cell carcinoma
Synonyms
  • H1581
  • H-1581
  • NCIH1581

02Classification

Organism
Human
Sex
Male
Growth properties
Adherent and suspension
Biosafety level
1

03Characteristics

Morphology
Epithelial-like

04Identifiers

Citation
NCI-H1581 (Cytion catalog number 305598)
NCBI TaxID
9606
Cellosaurus
CVCL_1479

05Handling and culture

Culture medium
DMEM:Ham's F12 (1:1), w: 3.1 g/L Glucose, w: 2.5 mM L-Glutamine, w: 15 mM HEPES, w: 0.5 mM Sodium pyruvate, w: 1.2 g/L NaHCO3 (Cytion article number 820400a)
Incubation atmosphere

37°C, 5% CO2, humidified atmosphere.

Supplements
Supplement the medium with 10% FBS
Dissociation reagent
Accutase
Seeding density
2-4*10^4/cm²
Thawing and culturing
  1. Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.

  2. Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required.

  3. For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains.

  4. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.

  5. Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently.

  6. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.

  7. Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks; for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth.

  8. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.

06Quality control and cryopreservation

Sterility

Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods.

To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections.

Freeze medium
As a cryopreservation medium, we recommend CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress.
Storage conditions

For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen.

Shipping conditions

Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage.

07Donor

Donor age
44 years
Ethnicity
Caucasian

09Product details

Composition table