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논문 기본 정보

자료유형
학술저널
저자정보
Kollipara, Pushpa Saranya (College of Pharmacy and Medical Research Center, Chungbuk National University) Kim, Jung Hyun (College of Korean Medicine, Gachon University) Won, Dohee (College of Pharmacy and Medical Research Center, Chungbuk National University) Lee, Sang Min (College of Pharmacy and Medical Research Center, Chungbuk National University) Sung, Ha Chang (College of Pharmacy and Medical Research Center, Chungbuk National University) Chang, Hyun Sok (College of Pharmacy and Medical Research Center, Chungbuk National University) Lee, Kang Tae (College of Pharmacy and Medical Research Center, Chungbuk National University) Lee, Kang Sik (College of Pharmacy and Medical Research Center, Chungbuk National University) Park, Mi Hee (College of Pharmacy and Medical Research Center, Chungbuk National University) Song, Min Jong (Department of Obstetrics and Gynecology, Daejeon St. Mary's Hospital, College of Medicine, The Catholic University of Korea) Song, Ho Sueb (College of Korean Medicine, Gachon University) Hong, Jin Tae (College of Pharmacy and Medical Research Center, Chungbuk National University)
저널정보
대한약학회 Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea 제37권 제3호
발행연도
2014.1
수록면
379 - 389 (11page)

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In the present study we experimented on a multimodal therapeutic approach, such as combining chemotherapy agent (Bee venom) with cellular (NK-92MI) immunotherapy. Previously bee venom has been found to show anti-cancer effect in various cancer cell lines. In lung cancer cells bee venom showed an $IC^{50}$ value of $3{\mu}g/ml$ in both cell lines. The co-culture of NK-92MI cell lines with lung cancer cells also show a decrease in viability upto 50 % at 48 h time point. Hence we used bee venom treated NK-92MI cells to co-culture with NSCLC cells and found that there is a further decrease in cell viability upto 70 and 75 % in A549 and NCI-H460 cell lines respectively. We further investigated the expression of various apoptotic and anti-apoptotic proteins and found that Bax, cleaved caspase-3 and -8 were increasing where as Bcl-2 and cIAP-2 was decreasing. The expression of various death receptor proteins like DR3, DR6 and Fas was also increasing. Concomitantly the expression of various death receptor ligands (TNFalpha, Apo3L and FasL) was also increasing of NK-92MI cells after co-culture. Further the DNA binding activity and luciferase activity of NF-${\kappa}B$ was also inhibited after co-culture with bee venom treated NK-92MI cell lines. The knock down of death receptors with si-RNA has reversed the decrease in cell viability and NF-${\kappa}B$ activity after co-culture with bee venom treated NK-92MI cells. Thus this new approach can enhance the anti-cancer effect of bee venom at a much lower concentration.

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