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6-gingerol이 소포체 스트레스에 의한 인간 전립선암 세포사멸에 미치는 효과

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Author(s)
조희영
Issued Date
2010
Keyword
6-gingerol
Abstract
Six-gingerol, one of the ginger (Zingiber officinale) compounds, has been shown to cause anti-tumor effects in a variety cancer cells including non-small cell lung cancer cells. Also, it previously reported that 6-gingerol inhibits cell proliferation in human breast cancer cells. Apoptosis is a major mechanism to eliminate cancer cells. The activation of caspase family and endoplasmic reticulum (ER) stress-mediated apoptotic pathway in the key step in apoptosis. The accumulation of unfolded or misfolded protein in ER can induce ER stress. To combat the deleterious effects of ER stress, cells have evolved various protective strategies, activate signal transduction pathways that trigger a complex transcriptional and translational response known as the unfolded protein response (UPR).
In this study, cells were treated with the doses of 6-gingerol for a variety time. 6-gingerol induced time -dependent reduced of cell viability in DU145 cells. Expression of cleaved caspase-3, capspase-4, and PARP protein involved in apoptotic cell death were increased in cell treated with 10μM 6-gingerol and shown to the typical apoptotic morphology of fragmentation and condensation after staining with Hoechst 33342. Also, GRP78, p-eIF2α, and CHOP expression were increased in DU145 cells. caspase-3 and NF-κB activity was significantly increased time-dependent in cell treated with 6-gingerol. Apoptosis-related protein, ER stress-related protein, caspase-3, and NF-κB activity were decreased expression in cell treated with PBA.
In conclusion, cells have shown that 6-gingerol induces apoptosis through ER stress in DU145 prostate cancer cells.
Alternative Title
6-Gingerol induces Apoptosis through increase of Endoplasmic Retuculum Stress in the Prostate cancer cells
Alternative Author(s)
Hee-young Cho
Affiliation
조선대학교 교육대학원 영양교육전공
Department
교육대학원 영양교육
Advisor
이명렬
Awarded Date
2011-02
Table Of Contents
목 차 1

도목차 3

ABSTRACT 5

Ⅰ. 서 론 7

Ⅱ. 재료 및 방법 11

1. 재료 11
2. 방법 12
1) 세포배양 12
2) 세포독성 실험 12
3) 세포사멸과 관련된 단백질 발현 검증 12
4) Caspase-3 활성 측정 13
5) Hoechst 33342 및 Immunofluorescent 염색 13
6) 소포체만 선택적 염색 14
7) 프로모터 활성 측정 14
8) mRNA 분리 및 RT-PCR 14
9) 통계처리 15

Ⅲ. 결 과 16

1. 세포사멸 측정 16
1-1. 전립선암 세포의 생존율 측정 16
1-2. 세포사멸에 관련된 단백질 발현 측정 17
1-3. 세포사멸에 관련된 Caspase-3 활성 측정 18
1-4. 세포사멸에 관련된 Hoechst 33342 염색 19

2. 소포체 스트레스 측정 20
2-1. 소포체 스트레스에 관련된 단백질과 mRNA 발현 측정 20
2-2. 소포체만 선택적 염색 21
2-3. XBP-1 mRNA 분할 측정 22

3. 소포체 스트레스 경로 차단 후 6-gingerol 효과 측정 23
3-1. 소포체 스트레스 차단 후 세포사멸에 관련된 단백질 발현 측정 23
3-2. 소포체 스트레스 차단 후 Caspase-3 활성 측정 24
3-3. 소포체 스트레스 차단 후 전립선암 세포의 생존율 25

4. NF-κB 신호전달 측정 26
4-1. NF-κB 프로모터 측정 26
4-2. 소포체 스트레스에 의한 NF-κB 프로모터 측정 27

Ⅳ. 고 찰 28

Ⅴ. 결 론 31

Ⅵ. 참고문헌 32
Degree
Master
Publisher
조선대학교 교육대학원
Citation
조희영. (2010). 6-gingerol이 소포체 스트레스에 의한 인간 전립선암 세포사멸에 미치는 효과.
Type
Dissertation
URI
https://oak.chosun.ac.kr/handle/2020.oak/15315
http://chosun.dcollection.net/common/orgView/200000240998
Appears in Collections:
Education > 3. Theses(Master)
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