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Updated: Sep 15, 2026

Utilization of the Soft Agar Colony Formation Assay to Identify Inhibitors of Tumorigenicity in Breast Cancer Cells
Published on: May 20, 2015
Inhibition of PC cell-derived growth factor (PCDGF, epithelin/granulin precursor) expression by antisense PCDGF cDNA
1Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, 20 North Pine Street, Baltimore, MD 21201-1180, USA.
Abstract:
PC-cell derived growth factor (PCDGF) is an 88-kDa growth factor originally purified from the highly tumorigenic teratoma PC cell line and corresponds to the epithelin/granulin precursor. In teratoma cells, PCDGF expression was shown to be essential for tumorigenicity. We have reported that PCDGF was expressed in estrogen receptor-positive (ER(+)) human mammary epithelial cells in an estrogen-dependent fashion. In this study, we have investigated PCDGF expression in human mammary epithelial cell lines ranging from immortalized nontumorigenic cells to ER(+) and ER(-) breast carcinoma cells. Northern and Western blot analyses indicated that PCDGF mRNA and protein expression was low in nontumorigenic cells and increased in human breast carcinomas cell lines in a positive correlation with their tumorigenicity. Treatment of the ER(-) MDA-MB-468 cells with anti-PCDGF neutralizing antibody resulted in a dose-dependent inhibition of their proliferation, suggesting that secreted PCDGF acted as an autocrine growth factor for breast carcinoma cells. We then examined the in vitro and in vivo growth properties of MDA-MB-468 cells, where PCDGF expression had been inhibited by antisense PCDGF cDNA transfection. Inhibition of PCDGF expression resulted in a reduced proliferation rate in vitro and a 60-80% reduction in colony formation. Tumor formation in vivo was dramatically inhibited in antisense cells with a 90% inhibition of tumor incidence and tumor weight. These results demonstrate the importance of PCDGF overexpression for the proliferation and tumorigenicity of ER(-) breast carcinomas and suggest that PCDGF overexpression may play an important role in human breast cancer.
Insights
PC-cell derived growth factor (PCDGF) promotes breast cancer growth and tumorigenicity. Inhibiting PCDGF significantly reduced tumor formation in preclinical models, highlighting its potential as a therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- PC-cell derived growth factor (PCDGF) is linked to tumorigenicity in teratoma cells.
- PCDGF expression is estrogen-dependent in estrogen receptor-positive (ER(+)) human mammary epithelial cells.
- PCDGF is structurally related to the epithelin/granulin precursor.
Purpose of the Study:
- To investigate PCDGF expression in various human mammary epithelial cell lines, from nontumorigenic to ER(+) and ER(-) breast carcinoma cells.
- To determine the role of PCDGF as an autocrine growth factor in ER(-) breast carcinoma cells.
- To evaluate the impact of PCDGF inhibition on the proliferation and tumorigenicity of breast cancer cells.
Main Methods:
- Northern and Western blot analyses to assess PCDGF mRNA and protein levels.
- Treatment with anti-PCDGF neutralizing antibody to study proliferation inhibition.
- Antisense PCDGF cDNA transfection to inhibit PCDGF expression in vitro and in vivo.
- Assessment of cell proliferation, colony formation, tumor incidence, and tumor weight.
Main Results:
- PCDGF expression levels correlated positively with tumorigenicity across cell lines.
- Neutralizing PCDGF antibody inhibited proliferation of ER(-) breast carcinoma cells.
- Inhibition of PCDGF expression via antisense cDNA reduced in vitro proliferation and colony formation.
- Antisense PCDGF cells showed significantly reduced tumor incidence (90%) and weight in vivo.
Conclusions:
- PCDGF overexpression is crucial for the proliferation and tumorigenicity of ER(-) breast carcinomas.
- Secreted PCDGF acts as an autocrine growth factor in breast cancer.
- PCDGF represents a potential therapeutic target for human breast cancer.
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