지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2024.6
- 수록면
- 81 - 87 (7page)
- DOI
- 10.33615/jkohs.2024.12.2.81
이용수
초록· 키워드
오류제보하기
Objectives: This study explored the effects of CGM treatment on malignant melanoma cells, specifically by focusing on its ability to induce apoptosis and alter the expression of proteins involved in epithelial-mesenchymal transition (EMT), a critical process in cancer metastasis.
Methods: To assess cell viability and proliferation rates, at MTT assay and colony formation assay were performed. FACS analysis was conducted to confirm cell apoptosis, and JC-1 fluorescent staining was executed. An invasion assay was performed to observe cell invasiveness, and protein expression was validated by western blot analysis.
Results: Our findings demonstrated that CGM treatment significantly induced apoptosis in malignant melanoma cells. Additionally, CGM treatment markedly reduced the invasiveness of melanoma cells, as observed in the invasion assays. Western blot analysis revealed that CGM modulated the expression of several critical proteins involved in EMT, thereby disrupting the EMT process which is essential for cancer metastasis.
Conclusions: The research findings indicate that CGM inhibits the growth of melanoma effectively induces apoptosis of cancer cells, and suppresses metastasis through EMT inhibition. Therefore, CGM demonstrates significant value as a potential cancer therapeutic agent.
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