• 제목/요약/키워드: HT-29

검색결과 575건 처리시간 0.028초

천일염으로 제조한 된장의 암세포 성장 억제효과 (Growth-inhibitory Effect of the Solar Salt-Doenjang on Cancer Cells, AGS and HT-29)

  • 이선미;장해춘
    • 한국식품영양과학회지
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    • 제38권12호
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    • pp.1664-1671
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    • 2009
  • 된장제조 시 사용되는 소금의 종류(천일염, 정제염)를 달리하여 제조한 된장을 각각 2개월, 16개월 동안 숙성시켜 소금의 종류 및 발효기간에 따른 된장의 항암활성을 조사하였다. 소금의 종류를 달리한 2개월 숙성 된장의 물 추출물과 메탄올 추출물은 모두 정상세포 BJ에 대해 세포독성을 보이지 않고 오히려 세포성장효과를 지니는 반면 2종의 암세포에 대해서는 높은 성장억제효과를 나타내었다. 최대 처리농도인 1 mg/mL에서 AGS의 경우 천일염된장의 물 추출물은 41%, 메탄올 추출물은 29%의 억제율을 보였고, 정제염된장은 물 추출물에서 29%, 메탄올 추출물은 32%의 억제율을 보였다. 동일 농도에서 HT-29의 경우 천일염된장의 물 추출물은 40%, 메탄올 추출물은 26%의 억제율을 보였고, 정제염된장의 물, 메탄올 추출물은 각각 24%, 27%의 억제율을 보여 AGS와 HT-29에 대해 천일염된장의 물 추출물은 억제효과가 매우 뛰어남을 확인하였다. 천일염과 정제염을 첨가하여 제조한 16개월 숙성 된장의 각각의 추출물의 경우도 모두 정상세포 BJ에 대해 세포성장효과를 보였으며 특이적으로 암세포 AGS와 HT-29에 대해서는 성장억제효과가 높음을 확인하였다. 소금의 종류에 따른 된장추출물의 암세포 성장억제효과를 비교해 보기 위하여 최대 처리 농도인 1 mg/mL로 비교해 보면 AGS의 경우 천일염된장의 물 추출물은 50%, 메탄올 추출물은 36%의 억제율을 보였고, 정제염된장의 물 추출물은 32%, 메탄올 추출물은 42%의 억제율을 보였다. 동일 농도에서 HT-29의 경우 천일염된장의 물, 메탄올추출물은 각각 44%, 30%의 억제율을 보였고, 정제염된장의 물, 메탄올 추출물은 각각 32%, 35%의 억제율을 보여 16개월 숙성 된장의 경우 천일염된장의 물 추출물이 암세포 성장억제효과가 더 높게 나타났으며, 2개월 숙성 된장에 비교해 16개월 숙성 된장의 추출물이 항암효과가 더 우수함을 확인하였다. 더 나아가 AGS에 각 된장의 물 추출물을 최대 1mg/mL의 농도로 처리하여 apoptosis 유발 여부를 측정한 결과 대조구에 비교해 모든 실험구에서 apoptosis를 유발함을 확인하였다. 특히 천일염된장의 물 추출물(7.00${\pm}$1.15cells)이 정제염된장의 물 추출물(3.00${\pm}$1.15 cells)보다 AGS에 대한 억제효과 및 apoptosis 유발이 더 높게 나타나 위결과로 볼 때 천일염된장이 매우 뛰어난 항암효과를 지님을 알 수 있었다.

Chemopreventive Effect of Protein Extract of Asterina pectinifera in HT-29 Human Colon Adenocarcinoma Cells

  • Shon Yun-Hee;Nam Kyung-Soo
    • Archives of Pharmacal Research
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    • 제29권3호
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    • pp.209-212
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    • 2006
  • We investigated the effect of protein extract of Asterina pectinifera on the activity of 4 enzymes that may playa role in adenocarcinoma of the colon: quinone reductase (QR), glutathione Stransferase (GST), ornithine decarboxylase (ODC), and cyclooxygenase (COX)-2. QR and GST activity increased in HT-29 human colon adenocarcinoma cells increased that had been exposed to 4 concentrations of the protein extract (80, 160, 200, and $240{\mu}g/mL$). Additionally, 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced ODC activity decreased significantly in cells exposed to the extract in concentrations of $160{\mu}g/mL$ (p<0.05), $200{\mu}g/mL$ (p<0.005), and $240{\mu}g/mL$ (p<0.005). TPA-induced COX-2 activity also decreased in cells exposed to extract concentrations of 10, 20, 40, and $60{\mu}g/mL$. COX-2 expression was also inhibited in cells exposed to this extract. These results suggest that this protein extract of A pectinifera has chemopreventive activity in HT-29 human colon adenocarcinoma cells, and therefore, may have the potential to function as a chemopreventive agent in human colorectal cancer.

Arctigenin Inhibits Etoposide Resistance in HT-29 Colon Cancer Cells during Microenvironmental Stress

  • Yoon, Sae-Bom;Park, Hae-Ryong
    • Journal of Microbiology and Biotechnology
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    • 제29권4호
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    • pp.571-576
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    • 2019
  • Microenvironmental stress, which is naturally observed in solid tumors, has been implicated in anticancer drug resistance. This tumor-specific stress causes the degradation of topoisomerase $II{\alpha}$, rendering cells resistant to topoisomerase $II{\alpha}$-targeted anticancer agents. In addition, microenvironmental stress can induce the overexpression of 78kDa glucose regulated protein (GRP78), which can subsequently block the activation of apoptosis induced by treatment with anticancer agents. Therefore, inhibition of topoisomerase $II{\alpha}$ degradation and reduction in GRP78 expression may be effective strategies for inhibiting anticancer drug resistance. In this study, we investigated the active compound arctigenin, which inhibited microenvironmental stress-induced etoposide resistance in HT-29 cells. Arctigenin was also highly toxic to etoposide-resistant HT-29 cells, with an $IC_{50}$ value of $10{\mu}M$ for colony formation. We further showed that arctigenin inhibited the degradation of topoisomerase $II{\alpha}$ and reduced the expression of GRP78. Thus, these results suggest that arctigenin is a novel therapeutic agent that inhibits resistance to etoposide associated with microenvironmental stress conditions.

붉은 양파 분말의 화학성분 및 생리활성 (Chemical Components and Biological Activities of Red Onion Powder)

  • 장주리;권선진;임선영
    • 한국식생활문화학회지
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    • 제24권6호
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    • pp.749-755
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    • 2009
  • We investigated the chemical components of red onion powder dried using the low temperature vacuum method and the inhibitory effects of solvent extracts of the dried red onion powder on the growth of HT-1080 human fibrosarcoma and HT-29 human colon cancer cells and $H_2O_2$-induced oxidative stress. The moisture content of the dried red onion powder was 17.95%, while the vitamin C content was 96 mg/100 g and the total phenols content was 39.1 mg/mL. The inhibitory effects of acetone with methylene chloride (A+M) and methanol (MeOH) extracts of the red onion powder on the growth of HT-1080 and HT-29 cancer cells increased in a dose dependent manner (p<0.05). The inhibitory effect was greater on the growth of HT-29 cells, while the A+M extracts had a higher inhibitory effect than the MeOH extracts. Treatment with the hexane, 85% aq. methanol, butanol and water fractions of the extract led to significant inhibition of the growth of both cancer cell lines (p<0.05). Among the fractions, the hexane and 85% aq. methanol fractions showed a greater inhibitory effect. To determine the protective effect on $H_2O_2$-induced oxidative stress, a DCFH-DA (dichlorodihydrofluorescin diacetate) assay was conducted. All fractions, including the crude extracts of dried red onion, appeared to lead to a significant reduction in the levels of intracellular reactive oxygen species (ROS), and these reductions occurred in a dose dependent fashion (p<0.05). Among the fractions, the 85% methanol fraction showed the greatest protective effect on the production of lipid peroxides.

The Inhibitory Effects of Korean Red Ginseng Saponins on 5- HT3A Receptor Channel Activity Are Coupled to Anti-Nausea and Anti-Vomiting Action

  • Kim Jong-Hoon;Lee Byung-Hwan;Jeong Sang Min;Nah Seung-Yeol
    • Journal of Ginseng Research
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    • 제29권1호
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    • pp.37-43
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    • 2005
  • We performed in vitro and in vivo studies to know whether the inhibitory effects of ginsenosides on $5-HT_{3A}$ receptor channel acctivity are coupled to anti-nausea and anti-vomiting action. In vitro study, we investigated the effect of compound K (CK) and M4, which are ginsenoside metabolites, on human $5-HT_{3A}$ receptor channel activity expressed in Xenopus oocytes using two-electrode voltage clamp technique. Treatment of CK or M4 themselves had no effect in both oocytes injected with $H_2O\;and\;5-HT_{3A}$ receptor cRNA. In oocytes injected with $5- HT_{3A}$ receptor cRNA, M4 treatment inhibited more potently 5-HT-induced inward peak current $(I_{5-HT})$ than CK with dose-dependent and reversible manner. The half-inhibitory concentrations $(IC_{50})$ of CK and M4 were $36.9\;\pm\;10.1\;and\;7.3\;\pm\;2.2\;{\mu}M$, respectively. The inhibition of $I_{5-HT}$ by M4 was non-competitive and voltage-independent. These results indicate that M4 might regulate $5-HT_{3A}$ receptors. In vivo experiments, injection of cisplatin (7.5 mg/kg, i.v.) induced both nausea and vomiting with 1 h latency. These episodes reached to peak after 2 h and persisted for 4 h. Pre-treatment of GTS (500 mg/kg, p.o.) significantly reduced cisplatin-induced nausea and vomiting by $51\;\pm\;8.4\;and\;48.8\;\pm\;6.4\%$ during 4 h compared to GIS­untreated group, respectively. These results show the possibility that in vitro inhibition of $5-HT_{3A}$ receptor channel activity by ginsenosides might be coupled to in vivo anti-emetic activity.

강유전 고분자를 첨가한 유기태양전지의 효율 특성 (The Efficiency Characteristics of the Ferroelectric Polymer Added Organic Solar-cells)

  • 박자영;정치섭
    • 한국전기전자재료학회논문지
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    • 제29권9호
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    • pp.589-594
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    • 2016
  • P3HT:PCBM bulk heterojunction solar cells added with ferroelectric polymer were fabricated and characterized. By incorporating P3HT:PCBM solar cell with P(VDF-TrFE) ferroelectric additive, the power conversion efficiency was increased up to nearly 50%. Photoacoustic analysis on this phenomena was carried out for the first time. Through this study, we find that the ferroelectricity of the polymer additive plays the key role in the enhancement of the power conversion efficiency of the organic solar cell by suppressing the non-radiative recombination of charge transfer exciton more effectively.

Flexural Properties of Heat-Treatment Samama (Anthocephalus macrophyllus) Wood Impregnated by Boron and Methyl Metacrylate

  • CAHYONO, Tekat Dwi;DARMAWAN, Wayan;PRIADI, Trisna;ISWANTO, Apri Heri
    • Journal of the Korean Wood Science and Technology
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    • 제48권1호
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    • pp.76-85
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    • 2020
  • This study was conducted to analyze the application of boron compounds, methyl methacrylate (MMA), and heat treatment (HT) on changes in the density, moisture content, and flexural properties of samama (Anthocephalus macrophyllus) wood. Samama wood was impregnated with borax (BX) and boric acid (BA) using a pressure method at 5 atm for 4 h. Afterwards, the wood was impregnated with MMA at the same pressure and duration. Finally, the samama wood was given HT at 90 ℃ and 180 ℃. The results indicate that there was a weight gain of 93.4% in the wood impregnated using BA and MMA monomer and HT at 90 ℃. Consequently, the wood's density increased by 82.3%. Increased MOE and MOR percentages of 32.2% and 29.4%, respectively, were also found. HT at 180 ℃ degraded the wood components and MMA, and consequently, the density, MOE, and MOR also decreased. The wood impregnated by BX, BA, and MMA, and subjected to HT also had decreased moisture content (MC). This research recommends that the application of boron (BX, BA) should be combined with an MMA monomer and HT at 90 ℃ as an alternative method to improve samama wood quality. If darker color is preferable, HT should be conducted at 180 ℃.

고려인삼중 지용성 성분이 인체암 세포의 수종 효소활성에 미치는 영향. (Effects of Petroleum Ether Extract of Ginseng Root on Some Enzyme Activity in Human Colon Cancer Cells)

  • 황우익;오수경
    • Journal of Ginseng Research
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    • 제10권1호
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    • pp.27-35
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    • 1986
  • 본 연구는 인삼중 지용성 성분이 인체암 세포의 증식억제와 암세포내 효소 활성에 미치는 영향을 구명하고자 실시하였다. 인체 장암 세포인 HRT-18, HCT-48 및 HT-29등을 대상으로 인삼추출물 처리시 각 암세포의 증식율과 암세포내 효소 즉, sucrase, lactase, maltase 및 trehalase등 disaccharidas 활성을 측정한 바 다음과 같은 결과를 얻었다. 1. HTR-18, HT-29 및 HCT-48의 doubling time은 각각 약 20, 22, 24시간이 및 되었다. 2. 각 암세포의 증식율은 배양액 중 CX 함량의 증가와 연장에 따라 점차 더 억제되었다. 3. 인삼 extract를 함유하는 배양액에서 배양된 HRT-18 및 HCT-48 암세포의 sucarse활성은 각각 362% 및 577% 증가하였고, lactase(317%, 334%), maltase(134% 및 153%) 및 trehalase(311% 및 203%) 활성도 다 같이 유의성있게 증가하였다.

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