Therapy Induced Senescent Tumor Cells Increase Cancer Stemness

DC Field Value Language
dc.contributor.advisor박태준-
dc.contributor.author김영삼-
dc.date.accessioned2022-11-29T02:32:32Z-
dc.date.available2022-11-29T02:32:32Z-
dc.date.issued2021-02-
dc.identifier.other30546-
dc.identifier.urihttps://dspace.ajou.ac.kr/handle/2018.oak/20072-
dc.description학위논문(석사)--아주대학교 일반대학원 :의생명과학과,2021. 2-
dc.description.tableofcontentsⅠ. INTRODUCTION 1 Ⅱ. MATERIALS & METHODS 4 Ⅲ. RESULT 7 Ⅳ. DISCUSSION 19 Ⅴ. REFERENCES 21-
dc.language.isoeng-
dc.publisherThe Graduate School, Ajou University-
dc.rights아주대학교 논문은 저작권에 의해 보호받습니다.-
dc.titleTherapy Induced Senescent Tumor Cells Increase Cancer Stemness-
dc.title.alternative치료에 의해 유도 된 노화종양세포는 암 줄기세포능이 증가한다.-
dc.typeThesis-
dc.contributor.affiliation아주대학교 일반대학원-
dc.contributor.alternativeNameYoung Sam Kim-
dc.contributor.department일반대학원 의생명과학과-
dc.date.awarded2021. 2-
dc.description.degreeMaster-
dc.identifier.localId1203449-
dc.identifier.uciI804:41038-000000030546-
dc.identifier.urlhttp://dcoll.ajou.ac.kr:9080/dcollection/common/orgView/000000030546-
dc.subject.keywordCancer Stemness-
dc.subject.keywordSenescent Tumor cell-
dc.description.alternativeAbstractTherapy Induced Senescent Tumor Cells Increase Cancer Stemness. Cellular senescence is defined as permanent cell cycle arrest (Alessio et al., 2019). Under the stressful condition such as physical and chemical insult, cell eventually turns into senescence (Kong et al., 2019). Therapy induced senescence is a type of cellular senescence induced by irradiation or chemotherapy (Joyner et al., 2006). Several previous studies showed increased expression of stem cell related properties with cellular senescence (Tsolou et al., 2019). Here, we proceeded research to prove cellular senescence induced by doxorubicin increases cancer cell stemness in human breast cancer. Senescence associated β-galactosidase assay and quantitative polymerase chain reaction analysis revealed BT474, a breast cancer cell line, showed senescence phenotype after treatment of doxorubicin expressing p16INK4A (Loh et al.). Following qPCR and western blot analysis also revealed a stem cell marker CD133 was increased with the senescence marker p16INK4A after treatment of doxorubicin (Dai et al., 2018) Flow cytometry showed the proportion of CD133 and p16INK4A doublepositive cells was increased after doxorubicin treatment. In this regard, senescent tumor cells caused by chemotherapy increase cancer cell stemness which is closely related to cancer relapse (Dou and Berger, 2018). It is anticipated that targeting senescent tumor cells is a new target to prevent cancer relapse.-
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Graduate School of Ajou University > Department of Biomedical Sciences > 3. Theses(Master)
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