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      Synergistic Effects of Bee Venom and Natural Killer Cells on B16F10 Melanoma Cell Growth Inhibition through IL-4-mediated Apoptosis

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      https://www.riss.kr/link?id=A104611158

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      다국어 초록 (Multilingual Abstract)

      Objectives : We investigated the synergistic effects of bee venom (BV) and natural killer (NK) cells on B16F10 melanoma cell apoptosis mediated by IL-4.
      Methods : We performed a cell viability assay to determine whether BV can enhance the inhibitory effect of NK-92MI cells on the growth of B16F10 melanoma cells, and western blot analysis to detect changes in the expression of IL-4, IL-4Rα, and other apoptosis-related proteins. EMSA was performed to observe the activity of STAT6. To confirm that the inhibitory effect of BV and NK cells was mediated by IL-4, the above tests were repeated after IL-4 silencing by siRNA (50 nM).
      Results : B16F10 melanoma cells co-cultured with NK-92MI cells and simultaneously treated by BV (5 μg/ml) showed a higher degree of proliferation inhibition than when treated by BV (5 μg/ml) alone or co-cultured with NK-92MI cells alone. Expression of IL-4, IL-4Rα, and that of other pro-apoptotic proteins was also enhanced after co-culture with NK-92MI cells and simultaneous treatment with BV (5 μg/ml). Furthermore, the expression of anti-apoptotic bcl- 2 decreased, and the activity of STAT6, as well as the expression of STAT6 and p-STAT6 were enhanced. IL-4 silencing siRNA (50 nM) in B16F10 cells, the effects of BV treatment and NK-92MI co-culture were reversed.
      Conclusion : These results suggest that BV could be an effective alternative therapy for malignant melanoma by enhancing the cytotoxic and apoptotic effect of NK cells through an IL-4-mediated pathway.
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      Objectives : We investigated the synergistic effects of bee venom (BV) and natural killer (NK) cells on B16F10 melanoma cell apoptosis mediated by IL-4. Methods : We performed a cell viability assay to determine whether BV can enhance the inhibitory e...

      Objectives : We investigated the synergistic effects of bee venom (BV) and natural killer (NK) cells on B16F10 melanoma cell apoptosis mediated by IL-4.
      Methods : We performed a cell viability assay to determine whether BV can enhance the inhibitory effect of NK-92MI cells on the growth of B16F10 melanoma cells, and western blot analysis to detect changes in the expression of IL-4, IL-4Rα, and other apoptosis-related proteins. EMSA was performed to observe the activity of STAT6. To confirm that the inhibitory effect of BV and NK cells was mediated by IL-4, the above tests were repeated after IL-4 silencing by siRNA (50 nM).
      Results : B16F10 melanoma cells co-cultured with NK-92MI cells and simultaneously treated by BV (5 μg/ml) showed a higher degree of proliferation inhibition than when treated by BV (5 μg/ml) alone or co-cultured with NK-92MI cells alone. Expression of IL-4, IL-4Rα, and that of other pro-apoptotic proteins was also enhanced after co-culture with NK-92MI cells and simultaneous treatment with BV (5 μg/ml). Furthermore, the expression of anti-apoptotic bcl- 2 decreased, and the activity of STAT6, as well as the expression of STAT6 and p-STAT6 were enhanced. IL-4 silencing siRNA (50 nM) in B16F10 cells, the effects of BV treatment and NK-92MI co-culture were reversed.
      Conclusion : These results suggest that BV could be an effective alternative therapy for malignant melanoma by enhancing the cytotoxic and apoptotic effect of NK cells through an IL-4-mediated pathway.

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      참고문헌 (Reference)

      1 Peter ME, "The CD95(APO1/Fas)DISC and beyond" 10 : 26-35, 2003

      2 The Korean society of Pathologists, "Textbook of Pathology" KMS 22-27, 2010

      3 AshkenaziA, "Targetingdeathanddecoyreceptors of the tumor necrosis factor superfamily" 2 : 420-430, 2002

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

      5 성희진, "Synergistic Effect of Natural Killer Cells and Bee Venom on Inhibition of NCI-H157 Cell Growth" 대한침구의학회 33 (33): 47-56, 2016

      6 Hilary S Warren, "NK cells and apoptosis" 77 : 64-75, 1999

      7 Zhenjian C, "NF-kappaB in Lung Tumorigenesis" 3 (3): 4258-4268, 2011

      8 Robert L. Tepper, "Murine Interleukin-4 display potent anti-tumor activity in vivo" 57 (57): 503-512, 1989

      9 Dave S. B. Hoon, "Modulation of Human Melanoma Cells by Interleukin-4 and in combination with γ-Interferon or α-Tumor Necrosis Factor" 51 (51): 2002-2008, 1991

      10 Liu S, "Melittin prevents liver cancercellmetastasisthroughinhibitionof the Rac1-dependent pathway" 47 : 1964-1973, 2008

      1 Peter ME, "The CD95(APO1/Fas)DISC and beyond" 10 : 26-35, 2003

      2 The Korean society of Pathologists, "Textbook of Pathology" KMS 22-27, 2010

      3 AshkenaziA, "Targetingdeathanddecoyreceptors of the tumor necrosis factor superfamily" 2 : 420-430, 2002

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

      5 성희진, "Synergistic Effect of Natural Killer Cells and Bee Venom on Inhibition of NCI-H157 Cell Growth" 대한침구의학회 33 (33): 47-56, 2016

      6 Hilary S Warren, "NK cells and apoptosis" 77 : 64-75, 1999

      7 Zhenjian C, "NF-kappaB in Lung Tumorigenesis" 3 (3): 4258-4268, 2011

      8 Robert L. Tepper, "Murine Interleukin-4 display potent anti-tumor activity in vivo" 57 (57): 503-512, 1989

      9 Dave S. B. Hoon, "Modulation of Human Melanoma Cells by Interleukin-4 and in combination with γ-Interferon or α-Tumor Necrosis Factor" 51 (51): 2002-2008, 1991

      10 Liu S, "Melittin prevents liver cancercellmetastasisthroughinhibitionof the Rac1-dependent pathway" 47 : 1964-1973, 2008

      11 Jung Hyun Park, "Melittin Suppresses PMA-Induced Tumor Cell Invasion by Inhibiting NF-κB and AP-1-Dependent MMP-9 Expression" 한국분자세포생물학회 29 (29): 209-215, 2010

      12 McCourt C, "Malignant melanoma : a pictorial review" 83 (83): 103-110, 2014

      13 Véronique B, "Is NF-κB a good target for cancer therapy? Hopes and pitfalls" 8 (8): 33-40, 2009

      14 Pattabhiraman S, "IL-4 Induces Apoptosis inA549 LungAdenocarcinoma Cells : Evidence for the Pivotal Role of 15-Hydroxyeicosatetraenoic Acid Binding to Activated Peroxisome Proliferator-Activated Receptor γTranscription Factor" 170 (170): 887-894, 2003

      15 Timmer T, "Fas receptor-mediated apoptosis. A clinical application" 196 : 125-134, 2002

      16 Obiri NI, "Expression of high-affinity IL-4 receptors on human melanoma, ovarian and breast carcinoma cells" 95 (95): 148-155, 1994

      17 Takeda K, "Essential role of Stat6 in IL-4 signalling" 380 : 627-630, 1996

      18 KischkelFC, "Cytotoxicity-dependent APO-1(Fas/CD95)-associated proteins form a death-inducing signaling complex(DISC)with the receptor" 14 : 5579-5588, 1995

      19 Pushpa Saranya Kollipara, "Co-culture with NK-92MI cells enhanced the anti-cancer effect of bee venom on NSCLC cells by inactivation of NF-jB" 대한약학회 37 (37): 379-389, 2014

      20 JemalA, "Cancer statistics, 2010" 60 (60): 277-300, 2010

      21 Choi KE, "Cancer Cell Growth Inhibitory Effect of Bee Venom via Increase of Death Receptor 3 Expression and Inactivation of NF-kappa B in NSCLC Cells" 6 : 2210-2228, 2014

      22 S Bogdanov, "Bee Venom: Composition, Health, Medicine: A Review" Bee product Science 1-11, 2016

      23 Jung Hyun Kim, "Bee Venom Enhanced Cytotoxic Effect of Natural Killer Cells on Human Lung Cancer Through Inducing Extrinsic Apoptosis" 대한침구의학회 31 (31): 111-119, 2014

      24 Park MH, "Anticancer effect of bee venom in prostate cancer cells through activation of caspase pathway via inactivation of NF-κB" 61 : 801-812, 2010

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      학술지 이력

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      연월일 이력구분 이력상세 등재구분
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      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.56 0.56 0.61
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.58 0.58 0.636 0.12
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