A non-tumorigenic epithelial cell line designated PCIAA, derived from a large pre-malignant colorectal adenoma from a patient with familial polyposis coli (also referred to as hereditary adenomatosis of the colon and rectum) has become immortal in vitro. PCIAA has been passaged in vitro continuously
Possible involvement of chromosome 1 in in vitro immortalization: Evidence from progression of a human adenoma-derived cell line in vitro
β Scribed by Christos Paraskeva; Amanda Harvey; Susan Finerty; Susan Powell
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 496 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
β¦ Synopsis
We have previously reported that continuous in vitro passage in the presence of 3T3 feeders of a non-tumorigenic adenoma-derived epithelial cell line, designated PCIAA, resulted in its becoming immortal. At early passage PCIAA was normal diploid, whereas every cell of PCIAA late passage had an isochromosome l(q) which led us to suggest that abnormalities of chromosome I may be involved in tumour progression. We now report the isolation of a 313-feederindependent variant of early-passage PCIAA, designated PCI AA/FI, which was immortal in vitro and remained nontumorigenic. Each cell of PCIAAIFI again has an isochromosome I(q), like the late-passage PCIAA. However, with PCI A N F I it IS the other chromosome I of the homologous pair which is involved in the formation of the isochromosome I(q). This is possible to determine because of the polymorphic centromeric heterochromatin on chromosome I of the earlypassage PCIAA. With the late-passage PCIAA (grown with 3T3 feeders) the homologue with the large C-band has given rise to an isachromosome I(q) whereas with P C I W F I it is the other homologue with the smaller C-band which has given rise to this isochromosome. Both the immortal PCI ANFI and the immortal PCIAA late passage, therefore, have independent abnormalities involving chromosome I. These results indicate that chromosome I may be involved in in vitro immortalization.
π SIMILAR VOLUMES
Human prostatic carcinoma frequently metastasizes to bone tissue and activates bone metabolism, especially bone formation, at the site of metastasis. It has been reported that an extract of prostatic carcinoma and conditioned medium (CM) of a human prostatic carcinoma cell line, PC-3, established fr
## Abstract Suppression subtractive hybridization (SSH) was applied to identify differentially expressed genes in the SV40LT immortalized human bronchial epithelial cell line YβBE, with normal human bronchial epithelial cells (HBEC) as a control. Two cDNA libraries of upβ and downregulated genes we