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두경부편평세포암종에서 니코틴의 약제내성 유발과 대책 : KB 세포주 및 betulinic acid를 중심으로

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Author(s)
허준
Issued Date
2006
Abstract
The aim of this study was to investigate the role of smoking on cancer chemotherapy and also clarify the effect of betulinic acid as a chemosensitizer. The author checked the apoptotic pathway after treatment of nicotine, and compared the effect of anticancer drugs such as cisplatin and etoposide in the presence or absence of nicotine in oral squamous cell carcinoma (SCC) KB cell line. Moreover, the author assessed the combination chemotherapeutic effect of betulinic acid with well-known chemotherapeutics in the presence or absence of nicotine. Nicotine induces Bad phosphorylation in association with suppression of apoptosis in KB cells. The inhibition rate of KB cells co-treated with anticancer drugs and nicotine was significantly decreased compared to anticancer drug only treated group. However, chemoresistance caused by nicotine was subjugated by combination of betulinic acid and chemotherapeutics. To sum up these results, the author could expect that nicotine may involved the chemoresistance and carcinogenesis via anti-apoptotic pathway in SCC, and chemotherapy for the SCC should be done in the absence of nicotine in the patients' blood. Moreover, betulinic acid could be an useful chemosensitizer to treat SCC or to overcome nicotine-induced chemoresistance in SCC.
Alternative Title
Nicotine-induced Chemoresistance in Head and Neck Squamous Cell Carcinoma and Strategy for Overcoming Resistance : on the basis of KB cell line and betulinic acid
Alternative Author(s)
Heo, Joon
Affiliation
조선대학교 대학원
Department
일반대학원 의학과
Advisor
남용
Awarded Date
2006-02
Table Of Contents
도목차 = i
Abstract = 1
서론 = 3
재료 및 방법 = 6
결과 = 10
고찰 = 13
결론 = 18
참고문헌 = 19
그림설명 = 23
그림 = 25
Degree
Doctor
Publisher
조선대학교 대학원
Citation
허준. (2006). 두경부편평세포암종에서 니코틴의 약제내성 유발과 대책 : KB 세포주 및 betulinic acid를 중심으로.
Type
Dissertation
URI
https://oak.chosun.ac.kr/handle/2020.oak/6138
http://chosun.dcollection.net/common/orgView/200000232886
Appears in Collections:
General Graduate School > 4. Theses(Ph.D)
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