|Immortalized cells and one oncogene in malignant transformation: old insights on new explanation.|
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|PMID: 21605454 Owner: NLM Status: MEDLINE|
|BACKGROUND: Nearly thirty years ago, it was first shown that malignant transformation with single oncogene necessarily requires the immortal state of the cell. From that time this thesis for the cells of human origin was not disproved. The basic point which we want to focus on by this short communication is the correct interpretation of the results obtained on the widely used human embryonic kidney 293 (HEK293) cells.
RESULTS: Intensive literature analysis revealed an increasing number of recent studies discovering new oncogenes with non-overlapping functions. Since the 1970s, dozens of oncogenes have been identified in human cancer. Cultured cell lines are often used as model systems in these experiments. In some investigations the results obtained on such cells are interpreted by the authors as a malignant transformation of normal animal or even normal human cells (as for example with HEK293 cells). However, when a cell line gains the ability to undergo continuous cell division, the cells are not normal any more, they are immortalized cells. Nevertheless, the authors consider these cells as normal human ones, what is basically incorrect. Moreover, it was early demonstrated that the widely used human embryonic kidney 293 (HEK293) cells have a relationship to neurons.
CONCLUSIONS: Thus, the experiments with established cell lines reinforce the notion that immortality is an essential requirement for malignant transformation that cooperates with other oncogenic changes to program the neoplastic state and substances under such investigation should be interpreted as factors which do not malignantly transform normal cells alone, but possess the ability to enhance the tumorigenic potential of already immortalized cells.
|Vadym M Kavsan; Anton V Iershov; Olena V Balynska|
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|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2011-05-23|
|Title: BMC cell biology Volume: 12 ISSN: 1471-2121 ISO Abbreviation: BMC Cell Biol. Publication Date: 2011|
|Created Date: 2011-06-14 Completed Date: 2011-09-19 Revised Date: 2011-12-21|
Medline Journal Info:
|Nlm Unique ID: 100966972 Medline TA: BMC Cell Biol Country: England|
|Languages: eng Pagination: 23 Citation Subset: IM|
|Department of Biosynthesis of Nucleic Acids, Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine, Kyiv, Ukraine. email@example.com|
|APA/MLA Format Download EndNote Download BibTex|
Cell Transformation, Neoplastic*
Proto-Oncogene Proteins / genetics*, metabolism
|0/LETMD1 protein, human; 0/Proto-Oncogene Proteins|
Journal ID (nlm-ta): BMC Cell Biol
Publisher: BioMed Central
Copyright ©2011 Kavsan et al; licensee BioMed Central Ltd.
Received Day: 22 Month: 2 Year: 2011
Accepted Day: 23 Month: 5 Year: 2011
collection publication date: Year: 2011
Electronic publication date: Day: 23 Month: 5 Year: 2011
Volume: 12First Page: 23 Last Page: 23
Publisher Id: 1471-2121-12-23
PubMed Id: 21605454
|Immortalized cells and one oncogene in malignant transformation: old insights on new explanation|
|Vadym M Kavsan1||Email: firstname.lastname@example.org|
|Anton V Iershov1||Email: email@example.com|
|Olena V Balynska1||Email: firstname.lastname@example.org|
1Department of Biosynthesis of Nucleic Acids, Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine, 150 Zabolotnogo Street, 03680 Kyiv, Ukraine
In 1983, Newbold and Overell showed that the acquisition of the immortal state was required, although not sufficient, for malignant transformation, thus proving multistage model of cancer . They had demonstrated that an oncogene could cause malignant transformation of immortalized NIH/3T3 cells. Further, many research groups demonstrated that 2 oncogenes being introduced simultaneously can cooperate in driving normal rodent cells to neoplastic state, in these pairs one of oncogenes induces immortality . However, the transformation of primary human cells by these oncogene pairs were unsuccessful because of the differences in telomere biology and regulation of cell senescence between human and murine cells. As it was reviewed by Hahn, 2002 , "these experiments reinforce the notion that immortality is an essential requirement for transformation that cooperates with other oncogenic changes to program the neoplastic state". In the June 2010 issue of BMC Cell Biology, volume 11 in the article by Ha et al.  the authors undertook their study with the aim to assess whether human cervical cancer oncogene (HCCR-1) overexpression alone converts normal human cells to malignantly transformed cells. For this study, the authors have chosen the human embryonic kidney 293 cells (also often referred to as 293 cells, HEK 293, or less precisely HEK cells) as a model of normal human cells. In conclusion, the authors wrote: "although researchers have been able to transform normal mouse cells into tumor forming cells by introducing several cooperating oncogenes into these cells, human cells have been resistant to such transformation. In this study, we converted normal cells into tumor cells by delivering HCCR-1 alone in combination with no other oncogenes".
However, as it is widely known, 293 cells were generated by Graham et al.  in early 70s by transformation of culture of normal human embryonic kidney cells with sheared human adenovirus type 5 DNA. Further genomic analysis showed that approximately 4.5 kilobases from the left arm of the viral genome became incorporated into human chromosome 19, resulting in decreased senescence of these cells . Thus, HEK293 is not a model for normal human cells; these cells are immortalized already by known oncogene but not malignant yet. Moreover, even NIH/3T3 cells, which authors  also used for their conclusions are not really normal mouse cells: NIH/3T3 cells originate from mouse embryonic fibroblasts (MEF), which have the ability to overcome cellular senescence and be spontaneously immortalized when cultured under certain conditions . The mechanism of this immortalization was not fully described, but it was proposed that p19ARF and MDM2 functionally inactivate both p53 and pRb pathways involved in cell senescence . NIH/3T3 can be oncogenically transformed by Ras alone , while for MEF transformation at least 2 oncogenes are necessary .
Interesting, that similar investigations on HEK293 or NIH/3T3 cell lines with other oncogenes which do not overlap in their intracellular function also show conversion into tumor cells with one oncogene alone [4,10-12]. It is quite difficult also to accept completely the interpretation of authors that they observed transdifferentiation in HEK293 cell line without further discussion. The matter is that previously Shaw et al.  demonstrated that "the widely used HEK293 cells have an unexpected relationship to neurons, a finding that may require reinterpretation of many previous studies in which it was assumed that HEK293 cells resembled more typical kidney epithelial cells" and may not be used as an in vitro model for kidney cell function.
Thus, the experiments with an established or immortalized cell line that has acquired the ability to proliferate indefinitely either through random mutation or deliberate modification, such as ectopic expression of different genes, reinforce the notion that immortality is an essential requirement for transformation that cooperates with other oncogenic changes to program the neoplastic state and that the substances under such kind of investigations should be interpreted as factors (in particular, oncogenes or oncoproteins) which not malignantly transform alone the normal cells, but possess the ability to enhance the tumorigenic potential of already immortalized cells.
Nevertheless, the article by Ha et al.  was published very timely because the findings about the origin of HEK293 and NIH/3T3 cell lines will require reinterpretation of many previous studies in which it was assumed that these and other immortalized cell lines resembled typical normal human or rodent cells.
All the authors contributed equally to the text.
This work was supported by budget topic of the Institute of Molecular Biology and Genetics "Functional characterization of genes associated with initiation and progression of glial and connective tissue tumors of human brain".
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