- Research article
- Open Access
Transdifferentiation-inducing HCCR-1 oncogene
- Seon-Ah Ha†1,
- Hyun K Kim†1,
- JinAh Yoo1,
- SangHee Kim1,
- Seung M Shin1,
- Youn S Lee2,
- Soo Y Hur3,
- Yong W Kim3,
- Tae E Kim3,
- Yeun J Chung4,
- Shin S Jeun5,
- Dong W Kim6,
- Yong G Park7,
- Jin Kim8,
- Soon Y Shin9,
- Young H Lee9 and
- Jin W Kim1, 3Email author
© Ha et al; licensee BioMed Central Ltd. 2010
- Received: 21 October 2009
- Accepted: 30 June 2010
- Published: 30 June 2010
Cell transdifferentiation is characterized by loss of some phenotypes along with acquisition of new phenotypes in differentiated cells. The differentiated state of a given cell is not irreversible. It depends on the up- and downregulation exerted by specific molecules.
We report here that HCCR-1, previously shown to play an oncogenic role in human cancers, induces epithelial-to-mesenchymal transition (EMT) and mesenchymal-to-epithelial transition (MET) in human and mouse, respectively. The stem cell factor receptor CD117/c-Kit was induced in this transdifferentiated (EMT) sarcoma tissues. This MET occurring in HCCR-1 transfected cells is reminiscent of the transdifferentiation process during nephrogenesis. Indeed, expression of HCCR-1 was observed during the embryonic development of the kidney. This suggests that HCCR-1 might be involved in the transdifferentiation process of cancer stem cell.
Therefore, we propose that HCCR-1 may be a regulatory factor that stimulates morphogenesis of epithelia or mesenchyme during neoplastic transformation.
- Cancer Stem Cell
- Systemic Mastocytosis
- Bovine Calf Serum
- Nude Mouse Tumor
The concept that genetic events cooperate to achieve malignant transformation was proposed over a decade ago. Primary rodent cells are efficiently converted into tumorigenic cells by the co-expression of cooperating oncogenes. However, similar experiments with human cells have consistently failed . In 1999, after more than 15 years of trying, researchers have managed to convert normal human cells into tumor cells by delivering telomerase catalytic subunit in combination with two oncogenes . Although malignant transformation of human cells by a single oncogene may not occur or may require specialized factors, we demonstrated that HCCR-1, associated with various types of human cancers, alone induced tumorigenic conversion of mouse cells .
We have identified a novel oncogene, human cervical cancer oncogene (HCCR), that was classified into 2 types: HCCR-1 (GenBank accession number AF 195651) and HCCR-2 (GenBank accession number AF 315598) . The HCCR-1 and HCCR-2 overexpressed cells were tumorigenic in nude mice and HCCR transgenic mice developed breast cancers and metastasis [3, 4]. Also, HCCR-1 was overexpressed in various types of human malignancies and was found to regulate the p53 tumor-suppressor gene negatively [3–6]. However, it is unknown how HCCR-1 contributes to the cellular and biochemical mechanisms of human tumorigenesis.
Cell transdifferentiation is characterized by loss of some phenotypesalong with acquisition of new phenotypes in differentiated cells. Differentiated cells are endowed with the capacity of transforming into cells of a different type having other functions . Gene expression in differentiated cells has long been considered an irreversible phenomenon that is established at the time of replication. Given that, although repressed, the same genetic framework is present in all cell types, a change in gene expression among differentiated cells was predictable in particular conditions.In fact, the differentiated state of a given cell is not irreversible.It depends on the up- and downregulation exerted by specificmolecules .
Recent research suggests that tumor formation may result from the development of cancer stem cells by the deregulation of normal self-renewal pathways of tissue stem cells. Numerous signalling pathways have been implicated in this process including Notch, Wnt, LIF (leukemia inhibitory factor), PTEN (phosphatase and tensin homologue deleted from chromosome 10), SHH (sonic hedgehog) and BMI1 [9–12]. The discovery of cancer stem cells in AML, breast cancer and some CNS tumors offers a new approach to understanding the biology of these conditions. Further study into these and other mechanisms controlling self-renewal pathways is needed to understand not only what drives tumor formation from cancer stem cells but also what mechanisms could be used to 'switch off' tumor formation .
We undertook this study with the following aims: 1) to assess whether HCCR-1 overexpression converts normal cells to malignant transformed cells; 2) to determine whether HCCR-1 is involved in transdifferentiation process and embryonic kidney development; 3) to examine the molecular alterations occurring in HCCR-1 induced tumorigenesis.
HCCR-1 is involved in tumorigenesis and transdifferentiation
Transforming activity of HCCR-1 in HEK-293 cells
Transfected DNA source
95% confidence intervals
In order to confirm the above data, we performed the immunofluorescence microscopy experiment in HEK-293 and HEK-293 stable clone for HCCR-1 (Additional file 1 Figure S1 A, B). The result showed that the parental HEK-293 cells express the vimentin but in a lower level than HCCR-1 stable HEK-293 clone. This suggests that the vimentin level is slightly increased after HCCR-1 transfection. We then analyzed other epithelial markers in HEK-293, HEK-293 clones stably transfected with HCCR-1, and HEK-293 cells transfected with the empty vector. E-cadherin, α-catenin, and β-catenin are essential for the maintenance of epithelial structures. To determine whether the over-expression of HCCR-1 alters the expression profiles of these molecules, we performed the western blotting analyses as follows (Additional file 2 Figure S1 C). The result demonstrates that all of these epithelial markers (E-cadherin, α-catenin, and β-catenin) are down-regulated only in HCCR-1 stable cell lines. Therefore, this data support that HCCR-1 induces EMT in transformed HEK-293 cells.
The oncogenic transformation of NIH/3T3 cells would typically be expected to develop sarcomas because NIH/3T3 cells are of mesenchymal origin . However, the tumors in nude mice derived from HCCR-1 stably transfected NIH/3T3 cells had both sarcomatous (Figure 1I) and epithelial features (Figure 1J). Histologically, the tumors showed poorly differentiated sarcoma with epithelial differentiation (carcinosarcoma) (Figure 1J). They were composed mostly of spindle cells forming long and short fasciles. In focal areas these cells were vaguely aggregated to form epithelial cell nest-like structures (arrows). Reticulin fibers enveloped individual spindle cells in the sarcomatous areas, but enveloped vague epithelial cell nests in the more carcinomatous areas (Figure 1K). For a morphologic comparison between HCCR-1-derived tumor cells and epithelial cells, we determined whether HCCR-1-derived tumor cells expressed epithelial cell markers, such as the epithelial membrane antigens (Figure 1L), cytokeratin 7 (Figure 1M), cytokeratin 8 (Figure 1N), cytokeratin 19 (Figure 1O), cytokeratin 20 (Figure 1P), and the mesenchymal marker vimentin (Figure 1Q). HCCR-1-derived tumor cells were positive for both epithelial and mesenchymal markers (Figures 1L-1Q). These results suggest that transdifferentiation (MET) occurred in HCCR-1 stably transfected NIH/3T3 cells derived from nude mice tumors. HCCR-1 might play multiple developmental roles by mediating a signal originating from the mesenchyme and received by epithelia. Mesenchymal signals are known to govern differentiation and morphogenesis of many epithelia, but the molecular nature of the signals is poorly understood. This expression pattern indicates that this mesenchymal factor can transmit morphogenetic signals in epithelia development and suggests a molecular mechanisim for mesenchymal epithelial interactions. This study indicates that the HCCR-1 oncogene may be a mesenchyme-derived cytokine that stimulates the morphogenesis of epithelia and mediates interactions between the mesenchyme and epithelia during neoplasia.
Induction of c-kit proto-oncogene product by HCCR-1
Embryonic kidney development
Co-expression of the human Met receptor, its ligand, and hepatocyte growth factor/scatter factor (HGF/SF), in NIH/3T3 fibroblasts causes cells to become tumorigenic in nude mice. The resultant tumors display lumen-like morphology, contain carcinoma-like focal areas with intercellular junctions resembling desmosomes, and co-express epithelial (cytokeratin) and mesenchymal (vimentin) cytoskeletal markers. The apparent MET of the tumor cells mimics the conversion that occurs during embryonic kidney development, suggesting that Met-HGF/SF signaling plays a role in this process as well as in tumors that express both epithelial and mesenchymal markers . Because acquisition of epithelial properties by the fibroblast-derived cells mimics the MET of cells during the organogenesis of the kidney , we investigated whether HCCR-1 is expressed in the developing kidney. Immunoblot analysis demonstrated that as probed by rabbit polyclonal anti-HCCR-1 serum, HCCR-1 began to be overexpressed at fetal 18-day, remaining high up to postnatal 14-day, and decreased to a very low level in adult rat kidney (Additional file 2 Figure S2 A). Sections of 20-day-old fetal rat kidney revealed that HCCR-1 antibody stained throughout the collecting ducts only (Additional file 1 Figure S2 B, medulla on the left side), which are derived from the ureteric bud . The developing nephrons in the cortex were not stained (Additional file 1 Figure S2 B, nephrogenic zone on the right side). But the basolateral plasma membranes of the developing collecting duct, which are derived from the ureteric bud, were especially reactive to HCCR-1 antibody (Additional file 1 Figure S2 C). Because nephrogenesis is stimulated by a distinct ureteric signal, diffusion-limited basolateral molecules , which trigger MET, we propose that the HCCR-1 product may be a mesenchyme-derived regulatory factor that stimulates morphogenesis of epithelia in the developmental process and mediates interactions between mesenchyme and epithelia during neoplastic transformation.
Molecular genetic alterations in the HCCR-1-induced tumorigenesis
The conversion of normal cells into tumor cells involves changes in the activity of a number of distinct different genes and proteins in a cell. 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 [8, 27–29]. In this study, ectopic expression of HCCR-1 alone results in direct tumorigenic conversion of HEK-293 cells in vitro and in vivo.
Because NIH/3T3 cell is of mesenchymal origin ,sarcoma would typically develop from oncogene-transformed NIH/3T3 . But, nude mice bearing HCCR-1 allograft display characteristics of epithelial carcinomas. Because acquisition of epithelial properties by the fibroblast-derived cells mimics the mesenchymal to epithelial conversion of cells during the organogenesis of the kidney , we investigated whether HCCR-1 is expressed in the developing kidney. The developing nephrons in the cortex were not stained. But the basolateral plasma membranes of the developing collecting duct, which are derived from the ureteric bud ,were especially reactive to HCCR-1 antibody. Because nephrogenesis is stimulated by a distinct ureteric signal, diffusion-limited basolateral molecules ,which trigger mesenchymal to epithelial conversion, we propose that the HCCR-1 product may be a mesenchyme-derived regulatory factor that stimulates morphogenesis of epithelia in the developmental process and mediates interactions between mesenchyme and epithelia during neoplastic transformation. Our study suggests that overexpression of HCCR-1 induces tumorigenesis, transdifferentiation and embryonic kidney development.
Transdifferentiation is a change from one differentiated phenotype to another involving morphological and functional phenotypic markers [31, 32]. The conversion of a cell phenotype is likely to be accomplished by selective enhancement of gene expression, which controls the terminal developmental commitment of cells .There is little known about 'master switch' genes that determine a specific differentiation pathway and have the potential to induce the process in a cell originally destined for a different differentiation pathway .HCCR-1 might play multiple developmental roles by mediating a signal originating from the mesenchyme and received by epithelia. Mesenchymal signals are known to govern differentiation and morphogenesis of many epithelia, but the molecular nature of the signals is poorly understood. This expression pattern indicates that this mesenchymal factor can transmit morphogenetic signals in epithelia development and suggests a molecular mechanisim for mesenchymal epithelial interactions.
There is evidence to indicate that tumors develop secondarily to abnormalities in PKC-mediated signal transduction .Reports show that PKC induces a marked increase in telomerase activity .Besides tumor cells typically have acquired damage to genes that directly regulate their cell cycles . Our study suggests that deregulation of HCCR-1 activity in mouse NIH/3T3 cells might result in the activation of PKC or telomerase, loss of particular cell cycle checkpoint controls, and downregulation of tumor suppressor egr-1, thereby predisposing NIH/3T3 cells to malignant conversion.
This present study suggests that HCCR-1 is an oncogene which induces the transformation of HEK293 and NIH3T3 cells. Likewise, our previous study also demonstrated that HCCR-1 is a mitochondrial out membrane protein and suppresses the apoptosis . Consistent with this previous work, this study also reveals the anti-apoptotic activity of HCCR-1 by reducing the expression of Egr-1, a direct regulator of multiple tumor suppressors including TGF beta1, PTEN, and p53. Therefore, both studies support that HCCR-1 is an oncogene either by suppressing apoptotic activities or by dysregulating Egr-1, telomerase, or PKC activity. Since key functions related to apoptosis or anti-apoptosis often occur in mitochondria, it is not too surprising that HCCR-1 localizes to the mitochondria.
In conclusion, we converted normal cells into tumor cells by delivering HCCR-1 alone in combination with no other oncogenes. EMT and MET occurred in HCCR-1-transfected tumor cells. In addition, HCCR-1 participates in induction of the c-kit proto-oncogene, in activation of PKC and telomerase activities, and cell cycle progression. While further studies are needed to characterize cellular functions and regulatory mechanisms, HCCR-1 protein is likely to be a candidate onco-developmental protein for cancer stem cell in the development of human cancer.
Cell lines, construction of expression vector, and DNA transfection
Human embryonic kidney (HEK) 293 (ATCC CRL-1573) and NIH/3T3 cells were obtained from the ATCC. HEK-293/HCCR-1-V5 cell lineswere maintained in DMEM (Gibco) containing 200 μg/ml G418, 10% FBS and 1% PenStrep (Gibco).
Expression vector containing the coding region of HCCR-1 was constructed as follows. First, the Sal I fragment was isolated from the prokaryotic expression vector, pCEV-LAC, which contains the entire HCCR-1 cDNA. Then, pcDNA3.1 (Invitrogen, CA) was digested with Xho I to make a compatible end with Sal I. A Sal I fragment containing the HCCR-1 coding sequence was inserted into the Xho I-digested pcDNA3.1. Lipofectamine (Gibco BRL, Rockville, MD) was used to introduce the HCCR-1 expression vector into HEK-293 cells.
Morphology and tumorigenecity
Newly established cells grown in culture flasks were photographed by phase-contrast microscopy. To analyze tumorigenecity, 5 ×10 6 cells were injected subcutaneously into the posterior lateral aspect of the trunk of mice (5-week-old athymic nu/nu on BALB/c background). Nude mice were sacrificed when the subcutaneous tumors reached 1.5-2.5 cm in diameter.
Five ×10 3 viable cells were suspended in 1 ml of 0.3% noble agar (Difco Laboratories Inc., Detroit, MI) made with complete media, and layered onto 0.6% agar in 35-mm plates. All samples were plated in quadruplicate. The number of cell colonies (>50 cells/cluster) was estimated on days 21-28.
Immunoblot analysis and immunohistochemistry
For immunoblot analysis, cells were lysed in Laemmli sample buffer. Proteins were separated by 10% SDS-PAGE and then electroblotted. The membranes were incubated with a rabbit polyclonal anti-HCCR-1 serum and proteins were revealed by an ECL-Western blot detection kit. We performed immunohistochemistry on cryosections (5-μm) incubated with anti-vimentin, anti-keratin, anti-EMA antibodies (DAKO), and polyclonal antibody raised against HCCR-1. Binding of primary antibody was visualized by biotinylated secondary antibody, avidin-horseradish peroxidase, and AEC as the chromogen.
PKC and telomerase activity assays
PKC activity was measured using the SignaTECT™ Protein Kinase C Assay System (Promega, Madison, WI). PKC activity was defined as the difference in counts per minute incorporated into substrate in the absence and presence of phospholipid. Telomerase activity was determined by using the telomerase PCR-ELISA kit (Boehringer Mannheim). Immortalized human kidney cells (293 cells) provided in the kit were used as the positive control. A negative control was provided for human 293 cells by pretreatment with RNase.
Cell cycle experiments
Cells cultured at mid-log phase were growth arrested by incubation in medium containing 0.5% bovine calf serum for 36 hours. Cells to be analyzed for DNA content were harvested following trypsinization, and fixed in 70% ethanol. Fixed cells were then stained with propidium iodide. In brief, 50 μg/ml of propidium iodide staining solution (Sigma) and 100 units per ml of RNase A (Boerhinger Mannheim) were added to 2 ×10 6 cells. After incubation for 1 hour, cellular DNA content was determined by fluorescence analysis at 488 nm using a FACS Caliber (Becton Dickinson). A minimum of 1 ×10 4 cells per sample was analyzed with Modfit 5.2 software.
Data was analyzed by use of SAS software (SAS Institute, Cary, NC). One-way analysis of variance was used for comparing various outcome measures (e.g., PKC or telomerase levels) in different experimental conditions. The mean values and 95% confidence intervals for the outcome variables are shown in relevant figures. All reported P values are two-sided and were considered to be statistically significant at the .05 level. P values for comparing the difference between groups are adjusted by Dunnett's multiple comparisons.
This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2009-0066496)
- Eguchi G, Kodama R: Transdifferentiation. Curr Opin Cell Biol. 1993, 5: 1023-1028. 10.1016/0955-0674(93)90087-7.View ArticlePubMedGoogle Scholar
- Strutz F, Muller GA, Neilson EG: Transdifferentiation. A new angle on renal fibrosis. Exp Nephrol. 1996, 4: 267-270.PubMedGoogle Scholar
- Ko J, Lee YH, Hwang SY, Lee YS, Shin SM, Hwang JH, Kim J, Kim YW, Jang SW, Ryoo ZY, Kim IK, Namkoong SE, Kim JW: Identification and differential expression of novel human cervical cancer oncogene HCCR-2 in human cancers and its involvement in p53 stabilization. Oncogene. 2003, 22: 4679-4689. 10.1038/sj.onc.1206624.View ArticlePubMedGoogle Scholar
- Ko J, Shin SM, Oh YM, Lee YS, Ryoo ZY, Lee YH, Na DS, Kim JW: Transgenic mouse model for breast cancer: induction of breast cancer in novel oncogene HCCR-2 transgenic mice. Oncogene. 2004, 23: 1950-1953. 10.1038/sj.onc.1207356.View ArticlePubMedGoogle Scholar
- Yoon SK, Lim NK, Ha S-A, Park YG, Choi JY, Chung KW, Sun HS, Choi MJ, Chung J, Wands JR, Kim JW: The human cervical cancer oncogene protein is a biomarker for human hepatocellular carcinoma. Cancer Res. 2004, 64: 5434-5441. 10.1158/0008-5472.CAN-03-3665.View ArticlePubMedGoogle Scholar
- Shin Min Seung, Chung Jun Yeun, Oh Tack Seong, Jeon Myung Hae, Hwang Jeong Lae, Namkoong Hong, Kim Kee Hyun, Cho Won Goang, Hur Young Soo, Kim Eung Tae, Lee Soo Youn, Park Gyu Yong, Ko Jesang, Kim Woo Jin: HCCR-1-interacting molecule "deleted in polyposis 1" plays a tumor-suppressor role in colon carcinogenesis. Gastroenterology. 2006, 130: 2074-2086. 10.1053/j.gastro.2006.03.055.View ArticlePubMedGoogle Scholar
- Land H, Parada LF, Weinberg RA: Tumorigenic conversion of primary embryo fibroblasts requires at least two cooperating oncogenes. Nature. 1983, 304: 596-602. 10.1038/304596a0.View ArticlePubMedGoogle Scholar
- Hahn WC, Counter CM, Lundberg AS, Beijersbergen RL, Brooks MW, Weinberg RA: Creation of human tumour cells with defined genetic elements. Nature. 1999, 400: 464-468. 10.1038/22780.View ArticlePubMedGoogle Scholar
- Dontu G, Al-Hajj M, Abdallah WM, Clarke MF, Wicha MS: Stem cells in normal breast development and breast cancer. Cell Prolif. 2003, 36 (Suppl. 1): 59-72. 10.1046/j.1365-2184.36.s.1.6.x.View ArticlePubMedGoogle Scholar
- Lessard J, Sauvageau G: BMI-1 determines the proliferative capacity of normal and leukemic stem cells. Nature. 2003, 423: 255-260. 10.1038/nature01572.View ArticlePubMedGoogle Scholar
- Pardal R, Clarke MF, Morrison SJ: Applying the principles of stem-cell biology to cancer. Nat Rev. 2003, 3: 895-902.View ArticleGoogle Scholar
- Reya T, Morrison SJ, Clarke MF, Weissman IL: Stem cells, cancer and cancer stem cells. Nature. 2001, 414: 105-111. 10.1038/35102167.View ArticlePubMedGoogle Scholar
- Spillane JB, Henderson MA: Cancer stem cells: a review. ANZ J Surg. 2007, 77 (6): 464-468. 10.1111/j.1445-2197.2007.04096.x.View ArticlePubMedGoogle Scholar
- Aaronson SA, Jainchill JL, Todaro GJ: Murine sarcoma virus transformation of BALB-3T3 cells: lack of dependence on murine leukemia virus. Proc Natl Acad Sci USA. 1970, 66: 1236-1243. 10.1073/pnas.66.4.1236.PubMed CentralView ArticlePubMedGoogle Scholar
- Yarden Y, Kuang WJ, Yang-Feng T, Coussens L, Munemitsu S, Dull TJ, Chen E, Schlessinger J, Francke U, Ullrich A: Human proto-oncogene c-Kit: a new cell surface receptor tyrosine kinase for an unidentified ligand. EMBO J. 1987, 6: 3341-3351.PubMed CentralPubMedGoogle Scholar
- Miettinen M, Lasota J: KIT (CD117): a review on expression in normal and neoplastic tissues, and mutations and their clinicopathologic correlation. Appl Immunohistochem Mol Morphol. 2005, 13 (3): 205-220. 10.1097/01.pai.0000173054.83414.22.View ArticlePubMedGoogle Scholar
- Karin M: Signal transduction form cell surface to nucleus in development and disease. FASEB J. 1992, 6: 2581-2590.PubMedGoogle Scholar
- Yasuda A, Sawai H, Takahashi H, Ochi N, Matsuo Y, Funahashi H, Sato M, Okada Y, Takeyama H, Manabe T: Stem cell factor/c-kit receptor signaling enhances the proliferation and invasion of colorectal cancer cells through the PI3K/Akt pathway. Dig Dis Sci. 2007, 52 (9): 2292-300. 10.1007/s10620-007-9759-7.View ArticlePubMedGoogle Scholar
- Cho GW, Shin SM, Namkoong H, Kim HK, Ha SA, Hur SY, Kim TE, Chai YG, Kim JW: The phosphatidylinositol 3-kinase/Akt pathway regulates the HCCR-1 oncogene expression. Gene. 2006, 384: 18-26. 10.1016/j.gene.2006.07.006.View ArticlePubMedGoogle Scholar
- Tsarfaty I, Rong S, Resau JH, Rulong S, da Silva PP, Vande Woude GF: The Met proto-oncogene mesenchymal to epithelial cell conversion. Science. 1994, 263: 98-101. 10.1126/science.7505952.View ArticlePubMedGoogle Scholar
- Saxen L: Organogenesis of the Kidney. 1987, Cambridge: Cambridge University Press, 88-128.View ArticleGoogle Scholar
- Barasch J, Pressler L, Connor J, Malik A: A ureteric bud cell line induces nephrogenesis in two steps by two distinct signals. Am J Physiol. 1996, 271: F50-61.PubMedGoogle Scholar
- Barasch J, Yang J, Ware CB, Taga T, Yoshida K, Erdjument-Bromage H, Tempst P, Parravicini E, Malach S, Aranoff T, Oliver JA: Mesenchymal to epithelial conversion in rat metanephros is induced by LIF. Cell. 1999, 99: 377-386. 10.1016/S0092-8674(00)81524-X.View ArticlePubMedGoogle Scholar
- Huang RP, Darland T, Okamura D, Mercola D, Adamson ED: Suppression of v-sis-dependent transformation by the transcription factor, Egr-1. Oncogene. 1994, 9: 1367-1377.PubMedGoogle Scholar
- Holt SE, Wright WE, Shay JW: Regulation of telomerase activity in immortal cell lines. Mol Cell Biol. 1996, 16: 2932-2939.PubMed CentralView ArticlePubMedGoogle Scholar
- Li H, Zhao L, Yang Z, Funder JW, Liu JP: Telomerase is controlled by protein kinase C alpha in human breast cancer cells. J Biol Chem. 1998, 273: 33436-33442. 10.1074/jbc.273.50.33436.View ArticlePubMedGoogle Scholar
- Hjelle B, Liu E, Bishop JM: Oncogene v-src transforms and establishes embryonic rodent fibroblasts but not diploid human fibroblasts. Proc Natl Acad Sci USA. 1988, 85: 4355-4359. 10.1073/pnas.85.12.4355.PubMed CentralView ArticlePubMedGoogle Scholar
- Ron D, Tronick SR, Aaronson SA, Eva A: Molecular cloning and characterization of the human dbl proto-oncogene: evidence that its overexpression is sufficient to transform NIH/3T3 cells. EMBO J. 1988, 7: 2465-2473.PubMed CentralPubMedGoogle Scholar
- May WA, Arvand A, Thompson AD, Braun BS, Wright M, Denny CT: EWS/FLI1-induced manic fringe renders NIH 3T3 cells tumorigenic. Nat Genet. 1997, 17: 495-497. 10.1038/ng1297-495.View ArticlePubMedGoogle Scholar
- Lieberman MW, Lebovitz RM: Neoplasia. Anderson's Pathology. Edited by: Damjanov I, Linder J. 1996, St. Louis, MO: Mosby, 518-Google Scholar
- Boukamp P: Transdifferentiation induced by gene transfer. Semin Cell Biol. 1995, 6: 157-163. 10.1006/scel.1995.0022.View ArticlePubMedGoogle Scholar
- Yuan S, Rosenberg L, Paraskevas S, Agapitos D, Duguid WP: Transdifferentiation of human islets to pancreatic ductal cells in collagen matrix culture. Differentiation. 1996, 61: 67-75. 10.1046/j.1432-0436.1996.6110067.x.View ArticlePubMedGoogle Scholar
- Beresford WA: Direct transdifferentiation: can cells change their phenotype without dividing?. Cell Differ. 1990, 29: 81-93. 10.1016/0922-3371(90)90026-S.View ArticleGoogle Scholar
- Benzil DL, Finkelstein SD, Epstein MH, Finch PW: Expression pattern of alpha-protein kinase C in human astrocytomas indicates a role in malignant progression. Cancer Res. 1992, 52: 2951-2956.PubMedGoogle Scholar
- Sherr CJ: Cancer cell cycles. Science. 1996, 274: 1672-1677. 10.1126/science.274.5293.1672.View ArticlePubMedGoogle Scholar
- Cho Goang-Won, Shin Min Seung, Kim Kee Hyun, Ha Seon-Ah, Kim Sanghee, Yoon Joo-Hee, Hur Young Soo, Kim Eung Tae, Kim Woo Jin: HCCR-1, a novel oncogene, encodes a mitochondrial outer membrane protein and suppresses the UVC-induced apoptosis. BMC Cell Biology. 2007, 8: 1-12. 10.1186/1471-2121-8-50.View ArticleGoogle Scholar
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