Abstract
Carcinoembryonic antigen (CEA) is a highly glycosylated cell surface glycoprotein belonging to the immunoglobulin superfamily. CEA has been involved in vitro in adhesion mechanisms, but little is known about the function of this glycoprotein in vivo in normal tissue differentiation and malignancy. With regard to the relationship between CEA expression and tissue differentiation, it has been reported that transfection of the CEA gene in a rat L6 myoblasts results in a complete block of myogenic differentiation. To extend investigation to the transformed myogenic counterpart and examine CEA effects on differentiation and malignancy outside the colon system, we have transfected the human CEA gene in human rhabdomyosarcoma cells. Human rhabdomyosarcoma cells transfected with the CEA gene correctly expressed membrane CEA anchored via glycosylphosphatidylinositol and secreted CEA in the medium. CEA gene transfer in human rhabdomyosarcoma cells, which display a limited differentiation ability, does not further inhibit myogenic differentiation or after in vitro proliferation or natural killer sensitivity. CEA transfection does not affect s.c. growth in nude mice, but the ectopic expression of CEA in human rhabdomyosarcoma cells can strongly inhibit their metastatic ability to lungs and adrenals after i.v. injection. The impairment of metastatic potential correlates with a reduction in the homotypic adhesion properties of the cells. These data suggest that CEA, in some systems, can interfere with intercellular adhesion and, at least for cells not metastatic to the liver, can act as anti-metastatic molecule.
| Original language | English |
|---|---|
| Pages (from-to) | 4503-4508 |
| Number of pages | 6 |
| Journal | Cancer Research |
| Volume | 56 |
| Issue number | 19 |
| Publication status | Published - Oct 1 1996 |
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ASJC Scopus subject areas
- Cancer Research
- Oncology
Cite this
Expression of transduced carcinoembryonic antigen gene in human rhabdomyosarcoma inhibits metastasis. / Landuzzi, Lorena; Frabetti, Flavia; Rossi, Ilaria; Griffoni, Cristiana; De Giovanni, Carla; Nicoletti, Giordano; Nanni, Patrizia; Miniero, Rita; Palmieri, Gabriella; Santoni, Angela; Lollini, Pier Luigi.
In: Cancer Research, Vol. 56, No. 19, 01.10.1996, p. 4503-4508.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Expression of transduced carcinoembryonic antigen gene in human rhabdomyosarcoma inhibits metastasis
AU - Landuzzi, Lorena
AU - Frabetti, Flavia
AU - Rossi, Ilaria
AU - Griffoni, Cristiana
AU - De Giovanni, Carla
AU - Nicoletti, Giordano
AU - Nanni, Patrizia
AU - Miniero, Rita
AU - Palmieri, Gabriella
AU - Santoni, Angela
AU - Lollini, Pier Luigi
PY - 1996/10/1
Y1 - 1996/10/1
N2 - Carcinoembryonic antigen (CEA) is a highly glycosylated cell surface glycoprotein belonging to the immunoglobulin superfamily. CEA has been involved in vitro in adhesion mechanisms, but little is known about the function of this glycoprotein in vivo in normal tissue differentiation and malignancy. With regard to the relationship between CEA expression and tissue differentiation, it has been reported that transfection of the CEA gene in a rat L6 myoblasts results in a complete block of myogenic differentiation. To extend investigation to the transformed myogenic counterpart and examine CEA effects on differentiation and malignancy outside the colon system, we have transfected the human CEA gene in human rhabdomyosarcoma cells. Human rhabdomyosarcoma cells transfected with the CEA gene correctly expressed membrane CEA anchored via glycosylphosphatidylinositol and secreted CEA in the medium. CEA gene transfer in human rhabdomyosarcoma cells, which display a limited differentiation ability, does not further inhibit myogenic differentiation or after in vitro proliferation or natural killer sensitivity. CEA transfection does not affect s.c. growth in nude mice, but the ectopic expression of CEA in human rhabdomyosarcoma cells can strongly inhibit their metastatic ability to lungs and adrenals after i.v. injection. The impairment of metastatic potential correlates with a reduction in the homotypic adhesion properties of the cells. These data suggest that CEA, in some systems, can interfere with intercellular adhesion and, at least for cells not metastatic to the liver, can act as anti-metastatic molecule.
AB - Carcinoembryonic antigen (CEA) is a highly glycosylated cell surface glycoprotein belonging to the immunoglobulin superfamily. CEA has been involved in vitro in adhesion mechanisms, but little is known about the function of this glycoprotein in vivo in normal tissue differentiation and malignancy. With regard to the relationship between CEA expression and tissue differentiation, it has been reported that transfection of the CEA gene in a rat L6 myoblasts results in a complete block of myogenic differentiation. To extend investigation to the transformed myogenic counterpart and examine CEA effects on differentiation and malignancy outside the colon system, we have transfected the human CEA gene in human rhabdomyosarcoma cells. Human rhabdomyosarcoma cells transfected with the CEA gene correctly expressed membrane CEA anchored via glycosylphosphatidylinositol and secreted CEA in the medium. CEA gene transfer in human rhabdomyosarcoma cells, which display a limited differentiation ability, does not further inhibit myogenic differentiation or after in vitro proliferation or natural killer sensitivity. CEA transfection does not affect s.c. growth in nude mice, but the ectopic expression of CEA in human rhabdomyosarcoma cells can strongly inhibit their metastatic ability to lungs and adrenals after i.v. injection. The impairment of metastatic potential correlates with a reduction in the homotypic adhesion properties of the cells. These data suggest that CEA, in some systems, can interfere with intercellular adhesion and, at least for cells not metastatic to the liver, can act as anti-metastatic molecule.
UR - http://www.scopus.com/inward/record.url?scp=10144228403&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=10144228403&partnerID=8YFLogxK
M3 - Article
C2 - 8813148
AN - SCOPUS:10144228403
VL - 56
SP - 4503
EP - 4508
JO - Journal of Cancer Research
JF - Journal of Cancer Research
SN - 0008-5472
IS - 19
ER -