Abstract |
In the present study, we examined whether or not macrophage colony-stimulating factor ( M-CSF; CSF-1) is involved in the growth and differentiation of human chorionic, hydatidiform mole and choriocarcinoma cells. M-CSF promotes the growth of early gestation chorionic cells, hydatidiform mole cells, and a human term placenta cell line (tPA30-1). However, the growth of choriocarcinoma cells, BeWo, Jar, Jeg-3, and NUC-1, was not influenced at all by M-CSF. M-CSF promoted the secretion of human chorionic gonadotropin (hCG) and human placental lactogen (hPL), which are secreted from differentiated trophoblast, from early gestation chorionic cells and from hydatidiform mole cells. However, the secretion of hCG and hPL from choriocarcinoma cells was not affected by M-CSF. When M-CSF localization was examined by immunohistochemical staining, M-CSF was detected in chorionic and hydatidiform mole cells, but was absent in choriocarcinoma cells. These results suggest that the growth and differentiation of normal chorionic and hydatidiform mole cells are M-CSF-dependent, while the growth and differentiation of choriocarcinoma cells are not.
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Authors | S Saito, T Ibaraki, M Enomoto, M Ichijo, K Motoyoshi |
Journal | Japanese journal of cancer research : Gann
(Jpn J Cancer Res)
Vol. 85
Issue 3
Pg. 245-52
(Mar 1994)
ISSN: 0910-5050 [Print] Japan |
PMID | 8188522
(Publication Type: Journal Article)
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Chemical References |
- Chorionic Gonadotropin
- Macrophage Colony-Stimulating Factor
- DNA
- Placental Lactogen
- Receptor, Macrophage Colony-Stimulating Factor
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Topics |
- Base Sequence
- Cell Differentiation
(drug effects)
- Cell Division
(drug effects)
- Cells, Cultured
- Choriocarcinoma
(metabolism, pathology)
- Chorion
(cytology, drug effects, metabolism)
- Chorionic Gonadotropin
(biosynthesis, drug effects)
- DNA
(analysis)
- Female
- Humans
- Hydatidiform Mole
(metabolism, pathology)
- Immunohistochemistry
- Macrophage Colony-Stimulating Factor
(pharmacology)
- Molecular Sequence Data
- Placental Lactogen
(biosynthesis, drug effects)
- Point Mutation
- Polymerase Chain Reaction
- Pregnancy
- Receptor, Macrophage Colony-Stimulating Factor
(biosynthesis, genetics)
- Trophoblasts
(cytology, drug effects)
- Tumor Cells, Cultured
- Uterine Neoplasms
(metabolism, pathology)
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