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      Induced Apoptosis in HeLa Human Cervical Adenocarcinoma by the Extract of the Marine Algae Symbiotic Fungus Chaetomium sp.

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      https://www.riss.kr/link?id=A103908173

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      다국어 초록 (Multilingual Abstract)

      Natural compounds from marine organisms have been reported to possess several biological activities for the anti-oxidation, anti-diabetes, anti-inflammation and chemo-prevention against several vascular diseases. In this study, the anti-cancer effects...

      Natural compounds from marine organisms have been reported to possess several biological activities for the anti-oxidation, anti-diabetes, anti-inflammation and chemo-prevention against several vascular diseases. In this study, the anti-cancer effects of the extract of marine algae symbiotic fungus Chaetomium sp. on human cervical adenocarcinoma (HeLa) cells were investigated. Treatment of the extract on HeLa cells inhibited the cell proliferation and viability (IC50: 0.5μM) in a dose-dependent manner. Morphological observation revealed round-up shape and cells were finally floating. Also, the extract induced the activation of caspase-3, -6, -7, –8 and the cleavage of poly (ADP-ribose) polymerase (PARP). The substantial increase in positively stained cleaved caspase-3 and PARP with nuclear condensation (detected by DAPI staining) indicated the induction of apoptotic cell death with the involvement of activated caspase-8. The extract also induced cell cycle arrest with the up and down-regulation of p21waf1/cip1 and phospho-Cdc2 (Tyr15), respectively. The results suggested that the marine microbial extract has a potential in cancer prevention by the inhibition of cell proliferation and the induction of apoptotic cell death.
      (Cancer Prev Res 16, 302-310, 2011)

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      참고문헌 (Reference)

      1 Ghobrial IM, "Targeting apoptosis pathways in cancer therapy" 55 : 178-194, 2005

      2 Kalimutho M, "Platinum-(IV)-derivative satraplatin induced G2/M cell cycle perturbation via p53-p21waf1/cip1-independent pathway in human colorectal cancer cells" 32 : 1387-1396, 2011

      3 Shimada K, "Phosphorylation of FADD is critical for sensitivity to anticancer drug-induced apoptosis" 25 : 1089-1097, 2004

      4 Osamu T, "Novel histone deacetylase inhibitor exhibits antitumor activity via apoptosis induction in oral squamous cell carcinoma" 2 : 215-221, 2011

      5 Zhang J, "MiR-145, a new regulator of the DNA fragmentation factor-45 (DFF45)-mediated apoptotic network" 9 : 211-220, 2010

      6 Gurib-Fakim A, "Medicinal plants: traditions of yesterday and drugs of tomorrow" 27 : 1-93, 2006

      7 Yu SW, "Mediation of poly (ADP-ribose) polymerase 1-dependent cell death by apoptosis-inducing factor" 297 : 259-263, 2002

      8 Boldin MP, "Involvement of MACH, a novel MORT1/FADD-interacting protease, in Fas/APO-1- and TNF receptor-induced cell death" 85 : 803-815, 1996

      9 Jensen PR, "High recovery of culturable bacteria from the surfaces of marine algae" 126 : 1-7, 1996

      10 Chinnaiyan AM, "FADD, a novel death domain-containing protein, interacts with the death domain of Fas and initiates apoptosis" 81 : 505-512, 1995

      1 Ghobrial IM, "Targeting apoptosis pathways in cancer therapy" 55 : 178-194, 2005

      2 Kalimutho M, "Platinum-(IV)-derivative satraplatin induced G2/M cell cycle perturbation via p53-p21waf1/cip1-independent pathway in human colorectal cancer cells" 32 : 1387-1396, 2011

      3 Shimada K, "Phosphorylation of FADD is critical for sensitivity to anticancer drug-induced apoptosis" 25 : 1089-1097, 2004

      4 Osamu T, "Novel histone deacetylase inhibitor exhibits antitumor activity via apoptosis induction in oral squamous cell carcinoma" 2 : 215-221, 2011

      5 Zhang J, "MiR-145, a new regulator of the DNA fragmentation factor-45 (DFF45)-mediated apoptotic network" 9 : 211-220, 2010

      6 Gurib-Fakim A, "Medicinal plants: traditions of yesterday and drugs of tomorrow" 27 : 1-93, 2006

      7 Yu SW, "Mediation of poly (ADP-ribose) polymerase 1-dependent cell death by apoptosis-inducing factor" 297 : 259-263, 2002

      8 Boldin MP, "Involvement of MACH, a novel MORT1/FADD-interacting protease, in Fas/APO-1- and TNF receptor-induced cell death" 85 : 803-815, 1996

      9 Jensen PR, "High recovery of culturable bacteria from the surfaces of marine algae" 126 : 1-7, 1996

      10 Chinnaiyan AM, "FADD, a novel death domain-containing protein, interacts with the death domain of Fas and initiates apoptosis" 81 : 505-512, 1995

      11 Cho JH, "Eupatilin, a dietary flavonoid, induces G2/M cell cycle arrest in human endometrial cancer cells" 49 : 1737-1744, 2011

      12 Niculescu AB 3rd, "Effects of p21waf1/cip1 at both the G1/S and the G2/M cell cycle transition: pRb is a critical determinant in blocking DNA replication and in preventing endore duplication" 18 : 629-643, 1998

      13 Pines J, "Cyclins and cyclin-dependent kinases: a biochemical view" 308 : 697-711, 1995

      14 Cho SH, "Compound K, a metabolite of ginseng saponin, induces apoptosis via caspase-8-dependent pathway in HL-60 human leukemia cells" 9 : 448-461, 2009

      15 Ozören N, "Cell surface death receptor signaling in normal and cancer cells" 13 : 135-147, 2003

      16 Järvinen K, "Caspase-8, c-FLIP, and caspase-9 in c-Myc-induced apoptosis of fibroblasts" 317 : 2602-2615, 2011

      17 Díaz GD, "Caspase -8 and apoptosisinducing factor mediate a cytochrome c-independent pathway of apoptosis in human colon cancer cells induced by the dietary phytochemical chlorophyllin" 63 : 1254-1261, 2003

      18 Schneider P, "Apoptosis induced by death receptors" 74 : 281-286, 2000

      19 Sithranga Boopathy N, "Anticancer drugs from marine flora: an overview" 214186-214204, 2010

      20 Zhang X, "Alpha-santalol, a chemopreventive agent against skin cancer, causes G2/M cell cycle arrest in both p53-mutated human epidermoid carcinoma A431 cells and p53 wild-type human melanoma UACC-62 cells" 3 : 220-234, 2010

      21 Los M, "Acitvation and caspase-mediated inhibition of PARP: a molecular switch between fibroblast necrosis and apoptosis in death receptor signaling" 13 : 978-988, 2002

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2022 평가예정 재인증평가 신청대상 (재인증)
      2019-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2018-12-01 평가 등재후보로 하락 (계속평가) KCI등재후보
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2013-10-14 학술지명변경 외국어명 : Cancer Prevention Research -> Journal of Cancer Prevention KCI등재
      2012-10-15 학회명변경 영문명 : Korean Association of Cancer Prevention -> Korean Society of Cancer Preveniton KCI등재
      2011-04-04 학술지명변경 외국어명 : Journal of Korean Association of Cancer Prevention -> Cancer Prevention Research KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2007-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2005-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.22 0.22 0.18
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.15 0.12 0.405 0.13
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