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      Chemoresistance of oxaliplatin through AKT-mTOR pathway in colon cancers = 대장암에서 AKT/mTOR 경로를 통한 옥살리플라틴 내성 발현에 관한 연구

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      https://www.riss.kr/link?id=T15530229

      • 저자
      • 발행사항

        Suwon : 아주대학교, 2020

      • 학위논문사항

        Thesis(M.A.) -- 아주대학교 대학원 , 약학과 , 2020

      • 발행연도

        2020

      • 작성언어

        영어

      • KDC

        518 판사항(6)

      • DDC

        615.1 판사항(23)

      • 발행국(도시)

        경기도

      • 형태사항

        ix, 34 leaves : illustrations (some color) ; 26 cm

      • 일반주기명

        Adviser: 김소희
        Includes bibliographies

      • UCI식별코드

        I804:41038-000000029688

      • 소장기관
        • 국립중앙도서관 국립중앙도서관 우편복사 서비스
        • 아주대학교 도서관 소장기관정보
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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Oxaliplatin is a third-generation platinum analog that can interfere with DNA replication and transcription by DNA damage. Continuous exposure of oxaliplatin resulted in resistance to oxaliplatin but no mechanisms of oxaliplatin-resistance were reported. In this study, oxaliplatin resistant cells were established using HCT116, HT29, SW480 and SW620 colon cancer cells by gradually increasing drug concentration up to a maximum of 2 µM at least for 3 month. The 50% inhibitory concentrations of cell growth (IC50) of oxaliplatin were 5.34, 9.88, 10.1 and 9.49-fold higher in oxaliplatin resistant HCT116, HT29, SW480, and SW620 cells, respectively, compared to their respective parental cells. One mechanism is that the expression of AKT and mTOR proteins were overexpressed in the oxaliplatin-resistant colon cancer cells. In addition, the expression of LC3B, an autophagy marker, decreased along with increasing AKT/mTOR signals, which caused the increase in glucose metabolism to produce energy for cell survival in oxaliplatin-resistant cancer cells. Taken together, oxaliplatin-resistance might be mediated through the activation of AKT/mTOR pathway in colon cancer cells, and AKT/mTOR might be a potential targets for oxaliplatin-resistance in human colon cancers.
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      Oxaliplatin is a third-generation platinum analog that can interfere with DNA replication and transcription by DNA damage. Continuous exposure of oxaliplatin resulted in resistance to oxaliplatin but no mechanisms of oxaliplatin-resistance were report...

      Oxaliplatin is a third-generation platinum analog that can interfere with DNA replication and transcription by DNA damage. Continuous exposure of oxaliplatin resulted in resistance to oxaliplatin but no mechanisms of oxaliplatin-resistance were reported. In this study, oxaliplatin resistant cells were established using HCT116, HT29, SW480 and SW620 colon cancer cells by gradually increasing drug concentration up to a maximum of 2 µM at least for 3 month. The 50% inhibitory concentrations of cell growth (IC50) of oxaliplatin were 5.34, 9.88, 10.1 and 9.49-fold higher in oxaliplatin resistant HCT116, HT29, SW480, and SW620 cells, respectively, compared to their respective parental cells. One mechanism is that the expression of AKT and mTOR proteins were overexpressed in the oxaliplatin-resistant colon cancer cells. In addition, the expression of LC3B, an autophagy marker, decreased along with increasing AKT/mTOR signals, which caused the increase in glucose metabolism to produce energy for cell survival in oxaliplatin-resistant cancer cells. Taken together, oxaliplatin-resistance might be mediated through the activation of AKT/mTOR pathway in colon cancer cells, and AKT/mTOR might be a potential targets for oxaliplatin-resistance in human colon cancers.

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      목차 (Table of Contents)

      • ABSTRACT i
      • TABLE OF CONTENTS ii
      • LIST OF FIGURES iv
      • LIST OF TABLES vi
      • ABBREVIATIONS vii
      • ABSTRACT i
      • TABLE OF CONTENTS ii
      • LIST OF FIGURES iv
      • LIST OF TABLES vi
      • ABBREVIATIONS vii
      • I. INTRODUCTION 1
      • II. MATERIALS AND METHOD 3
      • A. Chemicals 3
      • B. Cell culture and establishment of oxaliplatin-resistant cells 3
      • C. Cell proliferation assay 4
      • D. Flow cytometry analysis 4
      • E. Immunofluorescence analysis 5
      • F. Immunoblot analysis 5
      • G. Statistical analysis 6
      • III. RESULTS 7
      • A. Oxaliplatin-resistance of colon cancer cells 7
      • B. Drug efflux pump protein expression 10
      • C. Induction of cell cycle arrest by oxaliplatin 12
      • D. Protein expression on apoptosis and cell cycle 15
      • E. Induction of autophagy by oxaliplatin 17
      • F. Effect of oxaliplatin-resistance on AKT/mTOR pathway 19
      • G. Effect of oxaliplatin-resistance on glucose metabolism 21
      • IV. DISCUSSION 23
      • V. CONCLUSIONS 26
      • REFFERENCES 28
      • KOREAN ABSTRACT 33
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