Prolonged culture of telomerase-immortalized human fibroblasts leads to a premalignant phenotype

• Published in: Cancer research (Chicago, Ill.) Ill.), 2003-11, Vol.63 (21), p.7147-7157
• Main Authors: MILYAVSKY, Michael, SHATS, Igor, ROTTER, Varda, EREZ, Neta, XIAOHU TANG, SENDEROVICH, Shai, MEERSON, Ari, TABACH, Yuval, GOLDFINGER, Naomi, GINSBERG, Doron, HARRIS, Curtis C
• Format: Article
• Language: English
• Subjects: Antineoplastic agents; Biological and medical sciences; Cell Division - physiology; Cell Transformation, Neoplastic - metabolism; Cell Transformation, Neoplastic - pathology; Contact Inhibition; Cyclin-Dependent Kinase Inhibitor p16 - biosynthesis; Cyclin-Dependent Kinase Inhibitor p16 - genetics; DNA-Binding Proteins; Fibroblasts - cytology; Fibroblasts - enzymology; Gene Silencing; Genes, p53 - physiology; Genes, ras - physiology; Humans; Medical sciences; Pharmacology. Drug treatments; Precancerous Conditions - enzymology; Precancerous Conditions - pathology; Retinoblastoma Protein - genetics; Retroviridae - enzymology; Retroviridae - genetics; Telomerase - biosynthesis; Telomerase - genetics; Telomerase - metabolism; Time Factors; Transduction, Genetic; Tumor Suppressor Protein p14ARF - biosynthesis; Tumor Suppressor Protein p14ARF - genetics; Tumors
• ISSN: 0008-5472; 1538-7445

Telomere shortening in primary human fibroblasts results in replicative senescence, which can be overcome by telomerase (hTERT) overexpression. However, because immortalization is one of the hallmarks of malignant transformation, careful analysis of hTERT-immortalized cells is of crucial importance for understanding both processes. To this end, we infected WI-38 fibroblasts with a retrovirus carrying the hTERT cDNA and analyzed their proliferative behavior during 600 days [ approximately 500 population doublings (PDLs)] of continuous culture. Growth of three independent mass cultures was uniform for approximately 150 PDLs after telomerase infection, followed by a progressive acceleration of growth in two of three cultures. Expression of p16(INK4A) was significantly elevated in the immortalized cells but gradually disappeared during the accelerated growth phase. This alteration correlated with loss of the contact inhibition response and conferred the cells with sensitivity to H-Ras-induced transformation. In contrast, the p53- and pRb-mediated checkpoints such as the DNA damage response, chromosomal stability and entry into quiescence remained intact, irrespective of INK4A locus expression. Importantly, detailed examination of one of the WI-38/hTERT cultures during the accelerated growth phase revealed overexpression of the c-myc and Bmi-1 oncogenes, as well as loss of p14(ARF) expression. Collectively, our results indicate that although hTERT-immortalized cells behave similarly to primary cells during the first 150 PDLs, long-term growth in culture may favor the appearance of clones carrying potentially malignant alterations.