• 제목/요약/키워드: HT29 cells

검색결과 419건 처리시간 0.03초

전복 용매 추출물의 세포독성과 항산화 활성 (Cytotoxic and Antioxidant Activities of Abalone (Haliotis discus hannai) Extracts)

  • 임선영
    • 생명과학회지
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    • 제24권7호
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    • pp.737-742
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    • 2014
  • 본 연구에서는 전복을 동결 건조시킨 후 전복의 지방산을 비교 분석하였고 세포독성 활성 및 세포 내 활성산소종 생성 억제 효과를 측정하여 전복의 생리활성을 알아보고자 하였다. 지방산 조성 변화를 살펴보면 포화지방산들 내에서는 16:0의 함량이 건조 전복에서 높았고 불포화지방산들 내에서는 건조 전복의 경우 낮은 함량의 20:4n-6와 높은 함량의 22:6n-3를 나타내었다. 전복 A+M 추출물을 0.05 및 0.1 mg/ml 첨가농도로 HT-29 암세포에 처리했을 때 24%의 세포독성 효과를 나타내었다(p<0.05). MeOH 추출물의 경우 A+M 추출물과 비교했을 때 세포독성 효과가 낮았다. 건조 전복의 각 분획물을 농도별로 처리하였을 때, 농도의존적으로 세포독성 활성을 나타내었고, 특히 85% aq. MeOH 분획물에 의한 세포독성 활성이 가장 높았다(p<0.05). 세포 내 활성산소종 생성 억제효과에서 낮은 농도에서는 MeOH 추출물보다는 A+M 추출물에 의한 저해효과가 높았으며 분획물들 간 큰 차이는 없으나 85% aq. MeOH 분획물에 의한 생성 억제효과가 다소 높아 36%의 활성산소종 억제효과를 나타내었다.

Physicochemical Analysis of Yogurt Produced by Leuconostoc mesenteroides H40 and Its Effects on Oxidative Stress in Neuronal Cells

  • Lee, Na-Kyoung;Lim, Sung-Min;Cheon, Min-Jeong;Paik, Hyun-Dong
    • 한국축산식품학회지
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    • 제41권2호
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    • pp.261-273
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    • 2021
  • Leuconostoc mesenteroides H40 (H40) was isolated from kimchi, and its probiotic properties and neuroprotective effect was evaluated in oxidatively stressed SH-SY5Y cells. H40 was stable in artificial gastric conditions and can be attached in HT-29 cells. In addition, H40 did not produce β-glucuronidase and showed resistant to several antibiotics. The conditioned medium (CM) was made using HT-29 cells refined with heat-killed probiotics (Probiotics-CM) and heated yogurts (Y-CM) to investigate the neuroprotective effect. Treatment with H40-CM not only increased cell viability but also significantly improved brain derived neurotropic factor (BDNF) expression and reduced the Bax/Bcl-2 ratio in oxidatively stress-induced SH-SY5Y cells. Besides, probiotic Y-CM significantly increased BDNF mRNA expression and decreased Bax/Bcl-2 ratio. The physicochemical properties of probiotic yogurt with H40 was not significantly different from the control yogurt. The viable cell counts of lactic acid bacteria in control and probiotic yogurt with H40 was 8.66 Log CFU/mL and 8.96 Log CFU/mL, respectively. Therefore, these results indicate that H40 can be used as prophylactic functional dairy food having neuroprotective effects.

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.

Effect of Purified Green Tea Catechins on Cytosolic Phospholipase $A_2$ and Arachidonic Acid Release in Human Gastrointestinal Cancer Cell Lines

  • Hong, Jung-Il;Yang, Chung-S.
    • Food Science and Biotechnology
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    • 제15권5호
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    • pp.799-804
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    • 2006
  • Ingestion of green tea has been shown to decrease prostaglandin $E_2$ levels in human colorectum, suggesting that tea constituents modulate arachidonic acid metabolism. In the present study, we investigated the effects of four purified green tea catechins, (-)-epicatechin (EC), (-)-epigallocatechin (EGC), (-)-epigallocatechin-3-gallate (EGCG), and (-)-epicatechin-3-gallate (ECG), on the catalytic activity of cytosolic phospholipase $A_2$ ($cPLA_2$) and release of arachidonic acid and its metabolites from intact cells. At $50\;{\mu}M$, EGCG and ECG inhibited $cPLA_2$ activity by 19 and 37%, respectively, whereas EC and EGC were less effective. The inhibitory effects of these catechins on arachidonic acid metabolism in intact cells were much more pronounced. At $10\;{\mu}M$, EGCG and ECG inhibited the release of arachidonic acid and its metabolites by 50-70% in human colon adenocarcinoma cells (HT-29) and human esophageal squamous carcinoma cells (KYSE-190 and 450). EGCG and ECG also inhibited arachidonic acid release induced by A23187, a calcium ionophore, in both HT-29 and KYSE-450 cell lines by 30-50%. The inhibitory effects of green tea catechins on $cPLA_2$ and arachidonic acid release may provide a possible mechanism for the prevention of human gastrointestinal inflammation and cancers.

Antitumor Effects of Fucoidan on Human Colon Cancer Cells via Activation of Akt Signaling

  • Han, Yong-Seok;Lee, Jun Hee;Lee, Sang Hun
    • Biomolecules & Therapeutics
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    • 제23권3호
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    • pp.225-232
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    • 2015
  • We identified a novel Akt signaling mechanism that mediates fucoidan-induced suppression of human colon cancer cell (HT29) proliferation and anticancer effects. Fucoidan treatment significantly inhibited growth, induced G1-phase-associated upregulation of p21WAF1 expression, and suppressed cyclin and cyclin-dependent kinase expression in HT29 colon cancer cells. Additionally, fucoidan treatment activated the Akt signaling pathway, which was inhibited by treatment with an Akt inhibitor. The inhibition of Akt activation reversed the fucoidan-induced decrease in cell proliferation, the induction of G1-phase-associated p21WAF1 expression, and the reduction in cell cycle regulatory protein expression. Intraperitoneal injection of fucoidan reduced tumor volume; this enhanced antitumor efficacy was associated with induction of apoptosis and decreased angiogenesis. These data suggest that the activation of Akt signaling is involved in the growth inhibition of colon cancer cells treated with fucoidan. Thus, fucoidan may serve as a potential therapeutic agent for colon cancer.

Inhibitory Effect of Lactobacillus plantarum Extracts on HT-29 Colon Cancer Cell Apoptosis Induced by Staphylococcus aureus and Its Alpha-Toxin

  • Kim, Hangeun;Kim, Hye Sun;Park, Woo Jung;Chung, Dae Kyun
    • Journal of Microbiology and Biotechnology
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    • 제25권11호
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    • pp.1849-1855
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    • 2015
  • Staphylococcus aureus plays an important role in sepsis, septic shock, pneumonia, and wound infections. Here, we demonstrate that Lactobacillus plantarum extracts inhibited S. aureus-induced cell death of a human epithelial cell line, HT-29. In particular, we have shown that S. aureus-induced cell death was abolished by neutralization of α-toxin, indicating that α-toxin is the major mediator of S. aureus-induced cell death. DNA fragmentation experiment and caspase assay revealed that the S. aureus-induced cell death was apoptosis. L. plantarum extracts inhibited the generation of effector caspase-3 and the initiator caspase-9 in S. aureus- or α-toxin-induced cell death. Moreover, expression of Bcl-2, an anti-apoptotic protein, was activated in L. plantarum extract-treated cells as compared with the S. aureus- or α-toxin-treated only cells. Furthermore, S. aureus-induced apoptosis was efficiently inhibited by lipoteichoic acid and peptidoglycan of L. plantarum. Together, our results suggest that L. plantarum extracts can inhibit the S. aureus-mediated apoptosis, which is associated with S. aureus spreading, in intestinal epithelial cells, and may provide a new therapeutic reagent to treat bacterial infections.

Heptaphylline Induces Apoptosis in Human Colon Adenocarcinoma Cells through Bid and Akt/NF-κB (p65) Pathways

  • Boonyarat, Chantana;Yenjai, Chavi;Vajragupta, Opa;Waiwut, Pornthip
    • Asian Pacific Journal of Cancer Prevention
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    • 제15권23호
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    • pp.10483-10487
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    • 2015
  • Heptaphylline derivatives are carbazoles in Clausena harmandiana, a medicinal plant that is utilized for headache, stomach ache, and other treatments of illness. The present study examined the effects of heptaphylline and 7-methoxyheptaphylline on apoptosis of human colon adenocarcinoma cells (HT-29 cell line). Quantification of cell viability was performed using cell proliferation assay (MTT assay) and of protein expression through immunoblotting. The results showed that only heptaphylline, but not 7-methoxyheptaphylline, significantly significantly activated cleaved of caspase-3 and poly (ADP-ribose) polymerase (PARP-1) which resulted in HT-29 cell death. We found that heptaphylline activated BH3 interacting-domain death agonist (Bid) and Bak, proapoptotic proteins. In contrast, it suppressed X-linked inhibitor-of-apoptosis protein (XIAP), Bcl-xL and survivin, inhibitors of apoptosis. In addition, heptaphylline inhibited activation of NF-${\kappa}B$/p65 (rel), a regulator of apoptotic regulating proteins by suppressing the activation of Akt and $IKK{\alpha}$, upstream regulators of p65. The findings suggested that heptaphylline induces apoptosis in human colon adenocarcinoma cells.

Mithramycin Inhibits Etoposide Resistance in Glucose-deprived HT-29 Human Colon Carcinoma Cells

  • Lee, Eun-Mi;Park, Hae-Ryong;Hwang, Ji-Hwan;Park, Dong-Jin;Chang, Kyu-Seob;Kim, Chang-Jin
    • Journal of Microbiology and Biotechnology
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    • 제17권11호
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    • pp.1856-1861
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    • 2007
  • Physiological cell conditions such as glucose deprivation and hypoxia play roles in the development of drug resistance in solid tumors. These tumor-specific conditions cause decreased expression of DNA topoisomerase $II{\alpha}$, rendering cells resistant to topo II target drugs such as etoposide. Thus, targeting tumor-specific conditions such as a low glucose environment may be a novel strategy in the development of anticancer drugs. On this basis, we established a novel screening program for anticancer agents with preferential cytotoxic activity in cancer cells under glucose-deprived conditions. We recently isolated an active compound, AA-98, from Streptomyces sp. AA030098 that can prevent stress-induced etoposide resistance in vitro. Furthermore, LC-MS and various NMR spectroscopic methods identified AA-98 as mithramycin, which belongs to the aureolic acid group of antitumor compounds. We found that mithramycin prevents the etoposide resistance that is induced by glucose deprivation. The etoposide-chemosensitive action of mithramycin was just dependent on strict low glucose conditions, and resulted in the selective cell death of etoposide-resistant HT-29 human colon cancer cells.

단삼 추출물이 암세포주에 미치는 세포증식 억제 효과 (Antiproliferative Effect of the Salviae miltiorrhizae Radix Extracts on the Cancer Cell Lines)

  • 양의호;정태산;최창원
    • 대한한의학방제학회지
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    • 제22권2호
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    • pp.35-43
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    • 2014
  • Objectives : The purpose of this study was to identify antiproliferative effects of Salviae miltiorrhizae Radix(SM) extracts against cancer cell lines. Methods : We used 2 kinds of cancer cell lines such as colon cancer cells(HT-29), human oral epitheloid carcinoma cells(KB). MTT assay was performed to examine the efficacy of SM extracts on the cytostaticity of cancer cells in proportion to time and doses. Apoptosis was evaluated by DNA laddering and DAPI nuclei staining. Results : The MTT absorbances against HT-29 and KB of SM extracts were significantly decresed. DNA ladders could be identified in KB of SM extracts. The morphological change were observed and number of cells were decreased by SM extracts. Conclusions : SM extracts is considered to be effective to induce apoptosis and inhibit cancer cell proliferation.

Therapeutic Efficacy of Methanol Extract of Bidens tripartita in HT22 Cells by Neuroprotective Effect

  • Yerim Son;Choong Je Ma
    • Natural Product Sciences
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    • 제29권2호
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    • pp.67-73
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    • 2023
  • Oxidative stress brings about apoptosis through various mechanisms. In particular, oxidative stress in neuronal cells can causes a variety of brain diseases. This study was conducted to investigate the effect of Bidens tripartita on oxidative stress in neuronal cells. B. tripartita has traditionally been used in Russia as a medicine for diseases such as rhinitis, angina and colitis. Over-production of glutamate induces oxidative stress. When the oxidative stress occurs in the cells, reactive oxygen species (ROS) and Ca2+ increase. In addition, the abrupt decline of mitochondrial membrane potential and the decrease of glutathione related enzymes such as glutathione reductase (GR) and glutathione peroxidase (GPx) are also observed. The samples used in the experiment showed cytoprotective effect in the MTT assay. It also lowered the ROS and Ca2+ level, and increased degree of mitochondrial membrane potential, GR and GPx. As a result, B. tripartita had a positive effect against oxidative stress. Thus, it is expected to have potential for treatment and prevention of degenerative brain diseases such as Alzheimer's disease.