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Updated: Jul 16, 2026

In vitro Enrichment of Ovarian Cancer Tumor-initiating Cells
Published on: February 18, 2015
Combination antigene therapy targeting c-myc and c-erbB(2) in the ovarian cancer COC(1) cell line
1Department of Gynecologic Oncology, Zhongnan Hospital, Wuhan University, 169 Donghu Road, Wuhan, 430071, People's Republic of China.
Objective:
Antigene therapy targeting only one oncogene in ovarian cancer has made much progress, although it still has some limitations. To explore the potential for combination antigene therapy in ovarian cancer, we examined the in vitro effects of liposmal antisense phosphorothioate oligodeoxynucleotides targeting c-erbB(2) and c-myc (LF-c-erbB(2)/c-myc AS-ODNs) in the human ovarian cancer COC(1) cell line.
Methods:
COC(1) cells were treated differently as follows: group A with single LF-c-erbB(2) AS-ODNs; group B with single LF-c-myc AS-ODNs; group C with combination LF-c-erbB(2)/c-myc AS-ODNs; and group D as untreated control. Cell proliferation was studied by MTT assay and clonal cultures. RT-PCR was used to measure gene expression of c-erbB(2) and c-myc before and after transfection. Morphologic changes in the COC(1) cells were observed with the electron microscope.
Results:
Single antigene therapy targeting c-erbB(2) or c-myc could reduce target gene expression and inhibit COC(1) cell growth by 61.9 +/- 9.3 and 64.5 +/- 11.2%, respectively. However, combination antigene therapy could not only suppress expression of c-erbB(2) and c-myc simultaneously, but also inhibit COC(1) cell proliferation with a higher inhibitory rate of 82.6 +/- 12.1%. Apart from that, the combination agents could induce COC(1) cell apoptosis.
Conclusions:
Our study suggests that combination antigene therapy targeting c-erbB(2) and c-myc can inhibit COC(1) cell proliferation and gene expression of c-erbB(2) and c-myc. Furthermore, its effectiveness is much higher than that of individual antigene therapy.
Insights
Combination antigene therapy using liposomal antisense oligonucleotides targeting both c-erbB(2) and c-myc significantly inhibits ovarian cancer cell growth. This combined approach is more effective than single-target therapies, offering a promising strategy for ovarian cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Gene Therapy
Background:
- Antigene therapy shows promise for ovarian cancer but faces limitations with single-target approaches.
- Targeting oncogenes like c-erbB(2) and c-myc is a key strategy in cancer research.
Purpose of the Study:
- To investigate the in vitro efficacy of combination antigene therapy using liposomal antisense phosphorothioate oligodeoxynucleotides (LF-c-erbB(2)/c-myc AS-ODNs) in human ovarian cancer cells.
- To compare the effects of combined versus single-target antigene therapy on ovarian cancer cell proliferation and gene expression.
Main Methods:
- Human ovarian cancer COC(1) cells were treated with single LF-c-erbB(2) AS-ODNs, single LF-c-myc AS-ODNs, or combination LF-c-erbB(2)/c-myc AS-ODNs.
- Cell proliferation was assessed using MTT assay and clonal cultures.
- Gene expression of c-erbB(2) and c-myc was measured by RT-PCR, and morphologic changes were observed via electron microscopy.
Main Results:
- Single antigene therapies targeting c-erbB(2) or c-myc inhibited COC(1) cell growth by approximately 61.9% and 64.5%, respectively.
- Combination therapy demonstrated a higher inhibitory rate of 82.6% and simultaneously suppressed both c-erbB(2) and c-myc expression.
- Combination antigene therapy also induced apoptosis in COC(1) cells.
Conclusions:
- Combination antigene therapy targeting c-erbB(2) and c-myc effectively inhibits ovarian cancer cell proliferation and reduces target gene expression.
- The combined approach shows significantly greater efficacy compared to individual antigene therapies.
- This study supports combination antigene therapy as a potent strategy for ovarian cancer.
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