• 한국식품영양과학회지
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• 제37권3호
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• pp.288-293
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• 2008

막걸리의 암 예방효과를 알아보기 위하여 막걸리 농축물을 핵산, 메탄올, 부탄올 및 물로 순차적으로 분획하여 각 분획별로 암세포에 대한 성장 억제효과와 암 예방 지표인 QR활성 증가 효과를 측정하였다. 그 결과 메탄올 분획물의 경우 낮은 농도의 시료첨가에도 불구하고 괄목할 만한 높은 암세포 성장 억제효과를 나타내었으며 4종의 모든 암세포주 HepG2, B16-F10, HT29 및 MCF-7에서 농도 의존적인 암세포 성장 억제효과를 나타내었다. 또한 HepG2에서 측정한 QR활성 증가 효과에 있어서도 메탄올 분획물이 가장 높은 QR활성 증가 효과를 보여 암에 대한 예방효과가 기대된다. 따라서 앞으로 막걸리를 이용하여 항암관련 기능성식품을 개발할 수 있는 가능성이 보이며, 이를 위하여 특히 메탄올 분획물에 대한 집중적인 연구가 요구된다.

• 한국식품영양과학회지
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• 제36권9호
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• pp.1099-1105
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• 2007

오만둥이의 세포독성 효과를 알아보기 위해 신선한 오만둥이를 분쇄하고 동결건조하여 분말 형태로 제조한 후 시료 5 g당 메탄올, 에탄올, 아세톤, 물을 각각 100 mL씩 첨가하여 용매별 추출물을 제조하였다. 이 용매별 추출물을 대장암 세포주인 HT-29 cell에 250 ${\mu}g/mL$ 농도로 각각 처리하여 형태학적인 변화를 관찰한 결과 대조군에 비해 아세톤 추출물에서 세포의 수가 감소하고 그 형태가 응축되는 현상을 관찰할 수 있었고, 이 결과를 바탕으로 100, 250, 500 ${\mu}g/mL$ 농도로 MTT reduction assay를 실시한 결과 아세톤 추출물을 500 ${\mu}g/mL$ 농도로 처리했을 때 6%의 암세포만이 생존하는 것으로 나타나 형태학적인 실험결과와 동일한 결과를 얻을 수 있었다. 아세톤 추출물을 헥산, 디에틸 에테르, 에틸 아세테이트 그리고 물로 분획물을 조제하여 대장암 세포주인 HT-29 cell에 250 ${\mu}g/mL$ 농도로 각각 처리하여 형태학적인 변화를 관찰한 결과 헥산 분획물에서 세포의 형태변화가 가장 크게 나타났으며 250 ${\mu}g/mL$ 농도로 MTT reduction assay를 실시한 결과에서도 5.1%의 암세포만이 존재하는 것으로 나타나 헥산 분획물이 가장 높은 세포독성 효과를 보이는 것을 확인할 수 있었다. 다른 암세포주에 대한 영향을 알아보기 위해 헥산 분획물을 SW620, HeLa 및 MCF-7 세포주에 농도별로 처리한 결과, 250 ${\mu}g/mL$ 농도에서 10% 내외의 암세포 생존율을 보여 높은 세포독성 효과를 나타내었으며 특히, HeLa 세포주에서는 생존율이 5.8%로 나타나 매우 높은 활성을 보였다. 이상의 결과를 종합하여 미루어 짐작해 볼 때 오만둥이에 함유된 불포화 지방산 등의 지용성 물질이 암세포주의 성장 억제에 중요한 역할을 하리라 생각된다. 따라서 오만둥이 추출물은 다양한 암세포주에 대해 활성을 가지는 해양생물로서의 잠재적인 가능성을 가진다는 것을 확인할 수 있었다.

• Journal of Microbiology and Biotechnology
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• 제31권4호
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• pp.540-549
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• 2021

The Wnt/β-catenin signaling pathway is involved in breast cancer and Myxococcus fulvus KYC4048 is a myxobacterial strain that can produce a variety of bioactive secondary metabolites. Although a previous study revealed that KYC4048 metabolites exhibit anti-proliferative effects on breast cancer, the biochemical mechanism involved in their effects remains unclear. In the present study, KYC4048 metabolites were separated into polar and non-polar (ethyl acetate and n-hexane) fractions via liquid-liquid extraction. The effects of these polar and non-polar KYC4048 metabolites on the viability of breast cancer cells were then determined by MTT assay. Expression levels of Wnt/β-catenin pathway proteins were determined by Western blot analysis. Cell cycle and apoptosis were measured via fluorescence-activated cell sorting (FACS). The results revealed that non-polar KYC4048 metabolites induced cell death of breast cancer cells and decreased expression levels of WNT2B, β-catenin, and Wnt target genes (c-Myc and cyclin D1). Moreover, the n-hexane fraction of non-polar KYC4048 metabolites was found most effective in inducing apoptosis, necrosis, and cell cycle arrest, leading us to conclude that it can induce apoptosis of breast cancer cells through the Wnt/β-catenin pathway. These findings provide evidence that the n-hexane fraction of non-polar KYC4048 metabolites can be developed as a potential therapeutic agent for breast cancer via inhibition of the Wnt/β-catenin pathway.

• Natural Product Sciences
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• 제18권2호
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• pp.97-101
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• 2012

Six lignan compounds, 1-(17,21-dihydroxyphenyl)-9-(12,13-dihydroxyphenyl)-1-nonanone (malabaricone C) (1), 7'-(3',4'-methylenedioxyphenyl)-8,8'-dimethyl-7-(3,4-dihydroxyphenyl)-butane (2), 7'-(3',4'-dimethoxyphenyl)-8,8'-dimethyl-7-(3-methoxy-4-hydroxyphenyl)-butane (3), 7-(4-hydroxy-3-methoxyphenyl)-7'-(3',4'-methylenedioxyphenyl)-8,8'-lignan-7-methyl ether (4), (+)-erythro-(7S,8R)-${\Delta}^{8^'}$-7-hydroxy-3,4,3',5'-tetramethoxy-8-O-4'-neolignan (5), and (+)-erythro-(7S,8R)-${\Delta}^{8^'}$-7-acetoxy-3,4,3',5'-tetramethoxy-8-O-4'-neolignan (6), were isolated from the seeds of Myristica fragrans. The chemical structures of these compounds were determined on the basis of spectroscopic analyses including 2D NMR. Compounds 1 - 6 were evaluated for their cytotoxic activity against the HL-60, MCF-7, and A549 cancer cell lines in in vitro.

• Bulletin of the Korean Chemical Society
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• 제22권9호
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• pp.963-968
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• 2001

New anthracycline analogues 2-9 as potential anticancer agents have been synthesized from daunomycin (1a) and doxorubicin (1b). Compounds 2 and 6 were prepared by the nucleophilic displacement type esterification of 14-bromodaunomycin (1c) with N-benzoyl-(2R,3S)-phenylisoserine and L-pyroglutamic acid in triethyl-amine, respectively. Compounds 3, 7 and 4, 8 were prepared by the reaction of either daunomycin (1a) or doxorubicin (1b) with one equivalent of the corresponding acids in the presence of EDCI/PP. Compounds 5, 9 were obtained from 1b by reaction with 2.2 equivalents of the corresponding acids in the same manner. The cytotoxic activities of the analogues in comparison with adrimycin on cultured SNU-16 and MCF7 cell were described.

• Asian Pacific Journal of Cancer Prevention
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• 제15권24호
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• pp.10613-10619
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• 2015

Background: Both alcohol and aqueous extracts of Sauromatum giganteum(Engl.) Cusimano and Hett, the dried root tuber of which is named Baifuzi in Chinese, have been used for folklore treatment of cancer in Northeast of China. However, little is known about which is most suitable to the cancer therapy. Materials and Methods: Serum pharmacology and MTT assays were adopted to detect the effects of ethanol and aqueous extracts of Sauromatum giganteum(Engl.) Cusimano and Hett, prepared by heat reflux methods, on proliferation of different cancer cells. Results: Cancer cells treated with medium supplemented with 10%, 20%, 40% serum(v/v) containing ethanol extract had a decline in viability, with inhibition rates of 7.69%, 21.8%, 41.9% in MCF-7 cells, 42.8%, 48.1%, 51.8% in SGC-7901 cells, 44.1%, 49.2%, 53.7% in SMMC-7721 cells, 6.8%, 15.2%, 39.8% in HepG2 cells, 7.57%, 16.3%, 36.2% in HeLa cells, 6.24%, 12.5%, 27.4% in A549 cells, and 7.20%, 17.5%, 31.3% in MDA-MB-231 cells, respectively. Viability in the aqueous extract groups was no different with that of controls. Conclusions: An ethanol extract of Sauromatum giganteum(Engl.) Cusimano and Hett inhibited the proliferation of SMMC-7721, SGC-7901 and MCF-7 cells, which supports the use of alcoholic but not aqueous extracts for control of sensive cancers, which might include hepatocarcinoma, gastric cancer and breast cancer.

• 한국식품저장유통학회지
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• 제12권2호
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• pp.173-178
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• 2005

양파고추장에 대한 항암 및 면역활성을 조사한 결과는 다음과 같다. 고추장 메탄을 추출물은 aflatoxin $B_{1}$으로 돌연변이를 유도한 Salmonella typhimurium에 대하여 농도 의존적으로 항돌연변이 효과가 큰 것으로 나타났으며, 양파를 첨가하지 않은 대조구 고추장보다 양파고추장이 그 효과가 더욱 크게 나타났다. 양파고추장 메탄올추출물은 A549 및 MCF-7 암세포주에 처리한 결과 대조구에 비하여 $1,000\;{\mu}g/mL$농도에서 모두 $20\%$ 이상 그 성장을 억제하였다. 양파 고추장 메탄올추출물은 농도에 비례하여 비장세포의 증식을 유도하였고, 대조구 고추장 추출물보다 더 높은 증식을 유도하였다. 고추장 추출물을 처리한 대식세포주에서 NO의 생성이 농도 의존적으로 증가하였으며, 역시 양파고추장 추출물이 대조구 고추장 추출물보다 더 많은 NO을 생성량을 유도하였다.

• 한국환경성돌연변이발암원학회지
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• 제23권1호
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• pp.35-40
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• 2003

Polycyclic aromatic hydrocarbons (PAH) are frequently detected in food, water, soil, and sediment and are widespread environmental pollutants formed by the incomplete combustion of fossil fuels, woods and other organic matter. PAHs are considered to be probable human carcinogens. The mechanism of action of PAHs has been studied extensively, however it is not clear how PAHs turn on CYP1A1 in human breast cancer. Our laboratory have been studied the effect of PAHs in the human breast cancer cell MCF7. In this study, we examined the ZR-75-1 human breast cancer cells as a new system to evaluate bioactivity of PAHs. ZR-75-1 human breast cancer cell line responses to estrogen and progesteron. We have been able to estbilish long term culture system of this cells then used for the study to observe the effect of PAHs. We demonstrate that PAHs induced the CYP1A1 promoter and 7-ethoxyresolufin O-deethylase (EROD) activity in a concentration-dependant manner. RT-PCR analysis indicated that PAHs significantly up-regulate the level of CYP1A1 mRNA. Some of PAHs showed stronger stimulatory effect on CYP1 gene expression than TCDD. Apparently, ZR-75-1 cells have Aryl hydrocarbon receptors, therefore it would be good experimental tool to study the cross-talk between PAHs and steroid actions.

• 약학회지
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• 제42권5호
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• pp.507-512
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• 1998

In the course of developing novel antitumor intercalating agents. We synthesized 4-carbamoyloxymethyl-l-azaanthraquinones 7-12, incorporating the latent alkylating functi onality. These compounds were designed to explore the effect of substituent on the nitrogen of carbamate. The target compounds were prepared by hetero Diels-Alder reaction as a key step followed by functionalization of benzylic methyl to the desired substituents. Growth inhibitory studies of the azaanthraquinones were conducted in vitro against human cancer cell lines (SNU-354; liver and MCF7; breast) and human epidermoid carcinoma cells that are sensitive (KB-3-1) and multidrug-resistant (KB-V-1). The compounds were less potent than doxorubicin against sensitive cell lines. However, the most active compound 12 was not cross-resistant with doxorubicin against KB-V-1.

• Asian Pacific Journal of Cancer Prevention
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• 제13권12호
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• pp.6047-6053
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• 2012

Bracken fern [Pteridium aquilinem (L.) kuhn (Dennstaedtiaceae)] is one of the most common species on the planet. It has been consumed by humans and animals for centuries. Use by some human groups is because they believe bracken fern is good for health as plant medicine. However, it is also one of the few known plants that can cause tumors in farm animals. Many interested groups have focused their attention on bracken fern because of these interesting features. In order to evaluate the biological effects of exposure to this plant in cellular level, human cancer cell lines were treated with the fern dichloromethane extracts and the genotoxic and cytotoxic effects were studied. Anti-proliferative/cytotoxic effects were evaluated by cell count, MTT assay and flow cytometry methods with three different cancer cell lines, TCC, NTERA2, and MCF-7, and two normal cells, HDF1 and HFF3. Pro-apoptotic effects of the extracts were determined by DAPI staining and comet assay, on TCC cancer cells compared to the normal control cell lines. Cellular morphology was examined by light microscopy. Our present study showed that the extract caused DNA damage and apoptosis at high concentrations ($200{\mu}g/mL$) and also it may induce cell cycle arrest (G2/M phase) at mild concentrations (50 and $30{\mu}g/mL$) depending on the cell type and tumor origin. These results indicate that bracken fern extract is a potent source of anticancer compounds that could be utilized pharmaceutically.