Tumor Cell Lines

C-33 A

  • For research use only

Cat No.

ABC-TC0094

Product Type

Human Uterine Cancer Cell Lines

Cell Type

Epithelial

Species

Human

Growth Conditions

37 ℃, 5% CO2

Source Organ

Cervix

Disease

Cervical Cancer

Product Code

C33A; C33a; C33-A; C-33-A; C-33A; C33

C-33 A cell line is a human cervical carcinoma model widely used in HPV-related cancer research, drug screening, and tumor biology investigations.

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Description

C-33 A is a human cervical squamous carcinoma cell line originally isolated from the cervix of a 66-year-old Caucasian female patient. These cells exhibit an epithelial, adherent morphology and grow as a uniform monolayer. Cytogenetic analyses show a modal chromosome number of 46, with ~70% of cells exhibiting a pseudodiploid karyotype and occasional polyploid subpopulations. C-33 A harbors a TP53 point mutation at codon 273 (R→C), resulting in elevated mutant p53 protein expression. Additionally, this line is HPV-negative, with no detectable HPV DNA or RNA, making it valuable for studying non-viral cervical carcinogenesis. C-33 A is tumorigenic in vivo, forming undifferentiated carcinomas when xenografted into immunodeficient (nude) mice. The cells undergo rigorous screening and isolation procedures, and are rigorously tested to ensure they are free of contamination from HIV-1, HBV, HCV, Syphilis, Mycoplasma, Fungi, Yeast, and Bacteria.

Product Code

C33A; C33a; C33-A; C-33-A; C-33A; C33

Species

Human

Cat.No

ABC-TC0094

Product Category

Tumor Cell Lines

Size/Quantity

1 vial

Cell Type

Epithelial

Growth Mode

Adherent

Shipping Info

Dry Ice

Growth Conditions

37 ℃, 5% CO2

Source Organ

Cervix

Disease

Cervical Cancer

Biosafety Level

1

Storage

Liquid Nitrogen

Product Type

Human Uterine Cancer Cell Lines

Application

  • C-33 A cells are widely used in studies of HPV-independent cervical cancer biology, especially to investigate the role of TP53 mutations in cell cycle regulation, apoptosis, and tumorigenesis. Their unique metabolic profile, including altered lipid and fatty acid metabolism, provides insight into tumor metabolism and identifies potential metabolic vulnerabilities. Additionally, their tumorigenic nature of C-33A in mouse xenografts supports preclinical testing of novel therapies, especially those targeting p53-driven pathways and non-viral oncogenesis.

Citation

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