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JHH-7
Tissue
Liver
Disease
Adult hepatocellular carcinoma
Metastatic site
Primary liver tumor
Synonyms
Jhh-7, JHH7, FLC-7, FLC7, Functional Liver Cell-7

Documents

JHH-7

Cell line · Product number 305386

JHH-7 is a human hepatocellular carcinoma (HCC) cell line established from a primary HCC of a 53-year-old Japanese male patient, also designated FLC-7 (Fu...

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Customization / Recommendations

In stock
Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description

JHH-7 is a human hepatocellular carcinoma (HCC) cell line established from a primary HCC of a 53-year-old Japanese male patient, also designated FLC-7 (Functional Liver Cell-7). The line harbors a TP53 p.Arg267Pro mutation (unspecified zygosity), which affects the DNA-binding domain of p53 and impairs its tumor suppressor function. JHH-7 is one of several JHH-series HCC lines derived from Japanese patients at Jikei University, providing a well-characterized panel of HCC models with different TP53 mutational backgrounds and metabolic profiles.

JHH-7 is applicable in hepatocellular carcinoma research, including studies of HCC metabolism, hepatocyte differentiation markers, TP53 mutant tumor phenotype, drug sensitivity and resistance to sorafenib, lenvatinib, and other systemic HCC therapies, and comparative analyses within the JHH-series HCC panel. Its retained expression of liver-specific functions (albumin, AFP) makes it a relevant model for studying differentiated HCC biology. It is also applicable in xenograft studies.

Tissue
Liver
Disease
Adult hepatocellular carcinoma
Metastatic site
Primary liver tumor
Applications
Hepatocellular carcinoma research; HCC metabolism; TP53-mutant HCC biology; drug sensitivity (sorafenib, lenvatinib); JHH-series comparative studies; liver cancer drug evaluation; xenograft models
Synonyms
  • Jhh-7
  • JHH7
  • FLC-7
  • FLC7
  • Functional Liver Cell-7

02Classification

Organism
Human
Sex
Male
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
Epithelial-like
Cell type
Hepatocyte-like
Doubling time
26.4 hours ; 17.1 hours ; 30 hours , ~29 hours , ~26 hours

04Identifiers

Citation
JHH-7 (Cytion catalog number 305386)
NCBI TaxID
9606
Cellosaurus
CVCL_2805

05Expression and susceptibility

Mutational profile
Mutation: p.Arg267Pro, Unspecified

06Handling and culture

Culture medium
Williams' E medium or MEM + 10% FBS (verify from product CoA)
Incubation atmosphere

37°C, 5% CO2, humidified atmosphere.

Supplements
Supplement the medium with 10% FBS
Dissociation reagent
0.25% Trypsin-EDTA or Accutase
Subculturing
Remove medium, wash with PBS without calcium and magnesium, cover with 0.25% Trypsin-EDTA or Accutase, incubate 5–8 min at RT, resuspend in medium, centrifuge 300×g 3 min, discard supernatant, reseed in fresh medium.
Split ratio
1 to 5
Seeding density
1 to 3 × 10⁴ cells/cm²
Fluid renewal
Every 2 to 3 days
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 200 x g for 5 minutes, carefully discard the supernatant containing freezing medium.

  7. Follow the procedure described under Post-Thaw Recovery

07Quality control and cryopreservation

Freeze medium
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
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.

08Donor

Donor age
53 years
Ethnicity
Japanese