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자료유형
학술저널
저자정보
Mitupatum, Thantip (Faculty of Medicine, Thammasat University [Rangsit Campus]) Aree, Kalaya (Faculty of Medicine, Thammasat University [Rangsit Campus]) Kittisenachai, Suthathip (Thailand National Center for Genetic Engineering and Biotechnology [BIOTEC], Thailand Science Park) Roytrakul, Sittiruk (Thailand National Center for Genetic Engineering and Biotechnology [BIOTEC], Thailand Science Park) Puthong, Songchan (Antibody Production Research Unit, Institute of Biotechnology and Genetic Engineering, Chulalongkorn University) Kangsadalampai, Sasichai (Faculty of Medicine, Thammasat University [Rangsit Campus]) Rojpibulstit, Panadda (Faculty of Medicine, Thammasat University [Rangsit Campus])
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제16권 제5호
발행연도
2015.1
수록면
1,771 - 1,779 (9page)

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Hepatocellular carcinoma (HCC) is a leading cause of cancer death worldwide. Presently, targeted therapy via monoclonal antibodies to specific tumor-associated antigens is being continuously developed. Hep88 mAb has proven to exert tumoricidal effects on the HepG2 cell via a paraptosis-like morphology. To verify the pathway, we then demonstrated downstream up-regulation of caspase-3, caspase-8 and caspase-9, assessingmRNA expression by real-time PCR and associated enzyme activity by colorimetric assay. Active caspase-3 determination was also accomplished by flow cytometry. Active caspase-3 expression was increased by Hep88 mAb treatment in a dose-and time-dependent manner. All of the results indicated that Hep88 mAb induced programmed cell death in the HepG2 cell line from paraptosis-like to apoptosis by downstream induction of caspases. These conclusions imply that Hep88mAb might be a promising tool for the effective treatment of HCC in the future.

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