[Establishment of metastatic sub-clone from estrogen independent Ishikawa cells and its characterization in vitro and in vivo].

Abstract

An estrogen (E) independent sub-clone (EIIL) was separated from a human endometrial carcinoma cell line, Ishikawa, by culturing the wild type under an E free condition for 350 days. The cells were then implanted into nude mice subcutaneously and tumors allowed to develop for 35 days. The primary lesions were then excised to stimulate recurrence. One animal developed recurrence with multiple distant metastases. The primary tumor and metastatic tumors from the animal were studied for ErbB-2 expression by immunohystochemical techniques or by a reverse transcription followed by polymerase chain reaction (RT-PCR). Expressions of epidermal growth factor (EGF) receptors, aromatase, nidogen, E receptors, hepatocyte growth factors (HGF) and beta-actin were also examined. The results showed that metastatic lesions expressed high levels of ErbB-2, nidogen and aromatase but unchanged levels of EGF receptors and HGF. The metastatic lesions expressed one third of the E receptors which were detected in the EIIL in vitro. These observations suggest that a decrease in ER along with increased expression of nidogen and aromatase is associated with the process of metastasis and the model appears to be of value in studying the process of the acquisition of a metastatic phenotype.

• Authors: H Sakamoto, X Deng, T Shirakawa, S Ige, K Ohtani, A Saitoh, M Takami, T Takami, K Satoh
• Journal: Nihon Sanka Fujinka Gakkai zasshi (Nihon Sanka Fujinka Gakkai Zasshi) Vol. 47 Issue 3 Pg. 249-56 (Mar 1995) ISSN: 0300-9165 [Print] Japan
• PMID: 7699285 (Publication Type: Journal Article)

Chemical References

• Membrane Glycoproteins
• Receptors, Estrogen
• nidogen
• Hepatocyte Growth Factor
• Aromatase
• ErbB Receptors
• Receptor, ErbB-2

Topics

• Animals
• Aromatase (analysis)
• Base Sequence
• Clone Cells
• ErbB Receptors (analysis)
• Female
• Hepatocyte Growth Factor (analysis)
• Humans
• Membrane Glycoproteins (analysis)
• Mice
• Mice, Nude
• Molecular Sequence Data
• Neoplasm Metastasis
• Neoplasm Transplantation
• Neoplasms, Hormone-Dependent (metabolism, pathology)
• Receptor, ErbB-2 (analysis)
• Receptors, Estrogen (analysis)
• Tumor Cells, Cultured
• Uterine Neoplasms (metabolism, pathology)