사람 구강암세포에서 쿼세틴에 의한 항암 및 항전이 효과에 관한 융합연구
Convergence study on anticancer and antimetastasis effect by quercetin in human oral cancer cells
0
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
본 연구는 천연 플라보노이드계 물질인 쿼세틴을 사람 구강암세포주인 HSC-2 세포에 처리한 후 나타나는 항암 및 항전이 효과를 보기 위함이다. 연구 결과를 통하여 쿼세틴은 HSC-2 세포의 세포생존율 과 세포증식율이 감소하였으며, 이 세포 사멸의 경로는 세포 자살 프로그램인 세포자멸사의 경로를 통하여 일어나는 것임을 확인하였다. 또한 세포사멸에 큰 영향을 주지 않았던 농도인 쿼세틴 100 μM 처리군부터 HSC-2 세포의 이동력 과 침습력을 억제하는 효과가 있음을 확인하였다. 따라서 본 연구자는 종합적인 실험 결과를 통하여 구강암 세포에 있어서 200 μM이상의 쿼세틴 처리는 세포자살 프로그램을 가동하여 세포사멸을 유도하고, 100 μM 이상의 쿼세틴 처리는 세포의 이동과 침습을 억제하여 항암, 항전이 활성을 일으키는 것을 밝혔다. 그러므로 쿼세틴은 구강암에 있어 전이를 억제하고 암을 치료하기 위한 항암제로서 충분한 가치가 있음을 시사한다.
Abstract
This study was conducted to investigate the anticancer and antitumor effects of quercetin, which is a natural flavonoid substance in human oral cancer cell line HSC-2 cells. The results of this study showed that quercetin reduses the cell viability and the cell proliferation rate, and it led to the evidences of cell death through apoptosis pathway. Also, lower concetration quercetin over 100 μM were inhibited the cell migration and invasion. In the present study, we conclude that quercetin treatment of more than 200 μM induces apoptosis by activating programed cell death and quercetin treatment of 100 μM or more inhibits the cell migration and invasion rate in oral cancer cells. Therefore, this study suggests that quercetin is of sufficient value as an anticancer drug to inhibit metastasis and to treat cancer.
참고문헌 (24)
- S Franceschi, "Comparison of cancers of the oral cavity and pharynx worldwide: etiological clues", Oral Oncology, 36(1), pp.106~115 (2000), Elsevier BV[DOI]
- 한지형, "구강암의 발생현황과 원인", 치위생과학회지, 12(5), pp.451~458 (2012), 한국치위생과학회
- A. Jemal, "Cancer Statistics, 2010", CA: A Cancer Journal for Clinicians, 60(5), pp.277~300 (2010), Wiley[DOI]
- R. C. Budd, "An overview of apoptosis", Coron Artery Dis, 8(10), pp.593~597 (1997)
- Masaya Okura, "Decision analysis and treatment threshold in a management for the N0 neck of the oral cavity carcinoma", Oral Oncology, 45(10), pp.908~911 (2009), Elsevier BV[DOI]
- L. J. Talbot, "Epithelial-mesenchymal transition, the tumor microenvironment, and metastatic behavior of epithelial malignancies", Int J Biochem Mol Biol, 3(2), pp.117~136 (2012)
- 김영욱, "기저세포암과 편평세포암에서 E-cadherin 및Vimentin 발현에 의한 상피-간엽 전환", 대한피부과학회지, 53(2), pp.96~105 (2015), 대한피부과학회
- Jean-Jacques Monsuez, "Cardiac side-effects of cancer chemotherapy", International Journal of Cardiology, 144(1), pp.3~15 (2010), Elsevier BV[DOI]
- 노종현, "천초근 에탄올 추출물의 항산화 효능 및 대장암 세포 억제 효과", 한국자원식물학회지, 31(2), pp.102~108 (2018), 한국자원식물학회[DOI]
- 김은정, "삼백초 물 추출물과 유기용매 분획물의 항산화, 항염증 및 PMA에 의해 유도된 MMP-2 및 MMP-9활성 침윤 억제 효과", 생명과학회지, 26(5), pp.584~591 (2016), 한국생명과학회
- Giulia Di Carlo, "Flavonoids: Old and new aspects of a class of natural therapeutic drugs", Life Sciences, 65(4), pp.337~353 (1999), Elsevier BV[DOI]
- H. Michael Kubisch, "Targeted Overexpression of Cu", Zn Superoxide Dismutase Protects Pancreatic -Cells Against Oxidative Stress, 1997, pp.46(10), 1563~1566[DOI]
- 박봉수, "Luteolin Induces Apoptosis via Mitochondrial Pathway and Inhibits Invasion and Migration of Oral Squamous Cell Carcinoma by Suppressing Epithelial-Mesenchymal Transition Induced Transcription Factors", International Journal of Oral Biology, 43(2), pp.69~76 (2018), 대한구강생물학회
- 홍지영, "Induction of Cell Cycle Arrest and Apoptosis by Physcion, an Anthraquinone Isolated From Rhubarb (Rhizomes of Rheum tanguticum), in MDA-MB-231 Human Breast Cancer Cells", 대한암예방학회지, 19(4), pp.273~278 (2014), 대한암예방학회[DOI]
- J.-H. Yang, "INHIBITION OF LUNG CANCER CELL GROWTH BY QUERCETIN GLUCURONIDES VIA G2", M ARREST AND INDUCTION OF APOPTOSIS, 2005, pp.34(2), 296~304[DOI]
- M. Yoshizumi, "Quercetin inhibits Shc-and phosphatidylinositol 3-kinase-mediated c-Jun N-terminal kinase activation by angiotensin II in cultured rat aortic smooth muscle cells", Mol Pharmacol, 60(4), pp.656~665 (2001)
- J. L. Fernández-Luna, "Apoptosis regulators as targets for cancer therapy", Clinical and Translational Oncology, 9(9), pp.555~562 (2007), Springer Nature[DOI]
- S. Elmore, "Apoptosis: a review of programmed cell death", Toxicol Pathol, 35(4), pp.495~516 (2007)[DOI]
- L. Ouyang, "Programmed cell death pathways in cancer: a review of apoptosis, autophagy and programmed necrosis", Cell Proliferation, 45(6), pp.487~498 (2012), Wiley[DOI]
- J. K. Brunelle, "Control of mitochondrial apoptosis by the Bcl-2 family", Journal of Cell Science, 122(4), pp.437~441 (2009), The Company of Biologists[DOI]
- C Garrido, "Mechanisms of cytochrome c release from mitochondria", Cell Death and Differentiation, 13(9), pp.1423~1433 (2006), Springer Nature[DOI]
- Angeliki Voulgari, "Epithelial–mesenchymal transition in cancer metastasis: Mechanisms, markers and strategies to overcome drug resistance in the clinic", Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, 1796(2), pp.75~90 (2009), Elsevier BV[DOI]
- Raghu Kalluri, "The basics of epithelial-mesenchymal transition", Journal of Clinical Investigation, 119(6), pp.1420~1428 (2009), American Society for Clinical Investigation[DOI]
- Xiaoyu Li, "Pseudolaric Acid B Inhibits Proliferation, Invasion and Epithelial-to-Mesenchymal Transition in Human Pancreatic Cancer Cell", Yonsei Medical Journal, 59(1), pp.20~27 (2018), 연세대학교의과대학[DOI]
