• 제목/요약/키워드: SK-Hep1

검색결과 82건 처리시간 0.036초

젖소 초유 중 Insulin-like Growth Factor-I 분획이 암세포에 미치는 영향

  • 황경아;양희진;이수원
    • 한국축산식품학회:학술대회논문집
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    • 한국축산식품학회 2004년도 정기총회 및 제33차 춘계 학술대회
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    • pp.314-317
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    • 2004
  • IGF-I rich fraction 분리는 분만 후 24시간이내에 착유한 젖소 초유를 30kDa과 1kDa Ultrafiltra-tion(UF) membrane을 이용하여 분리하였다. 분리한 IGF-I rich fraction은 sandwich ELISA로 정량한 결과 1mg/ml 각 암세포에 미치는 영향을 실험하였다. 그 결과IGF-I rich fraction $1mg/m{\ell}$의 농도로 처리하였을 때 A-427ce11은 33%, SK-HEP-1 cell은 약 2%, A498 cell은 약 22%의 암세포 성장저해 효과를 보였고 HeLa는 약 5% 이하의 세포 증식 저해율과 WiDr cell은 약 30%의 세포성장 저해율을 나타내었으며, 유일하게 위암 세포주인 SNU 16에 대해서는 $1mg/m{\ell}$$100{\mu}g/m{\ell}$$10{\sim}1{\mu}g/m{\ell}$의 농도에서 약 15%와 10% 및 약 5% 이하의 세포 증식율을 나타내었다.

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Aloe vera가 항암제의 세포독성에 미치는 영향 (Effects of Aloe vera on the Cytotoxicity of Anticancer Drugs in Vitro)

  • 표명윤;윤지현
    • 약학회지
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    • 제43권1호
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    • pp.104-110
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    • 1999
  • We investigated effects of methanol extract of Aloe vera on anticancer drugs(cisplatin, mitomycin C, 5-fluorouracil)-induced growth inhibition in p388, L1210, HCT-15, SK-HepG-1 as cancer cell lines and mouse splenocytes as a normal cell by MTT assay, respectively. We also examined the effects of aloe extract and mitomycin C on the mitogen(Con, A, LPS)-induced splenocyte proliferation. Aloe extract(0.25 mg/m , 1.25 mg/m , 2.5 mg/m , 5.0 mg/m ) showed dose-dependently selective cytotoxicity against the cancer cell lines. In contrast, Aloe extract increased the growth and proliferation of the normal mouse splenocytes. The combination of aloe extract with anticancer drugs showed an additive effect for the cytotoxicity against cancer cell lines. However, that combination reduced clealy the anticancer drugs-induced toxicity against the normal mouse splenocytes.

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Caspase-3-mediated cleavage of Cdc6 induces nuclear localization of truncated Cdc6 and apoptosis

  • Yim, Hyung-Shin;Jin, Ying-Hua;Park, Byoung-Duck;Lee, Seung-Ki
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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    • pp.71.1-71.1
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    • 2003
  • We show that Cdc6, an essential initiation factor for DNA replication, undergoes caspase-3-mediated cleavage in the early stages of apoptosis in HeLa cells and SK-HEP-1 cells induced by etoposide, paclitaxel, ginsenoside Rh2, or TRAIL. The cleavage occurs at the SEVD$\^$442//G motif and generates an N-terminal truncated Cdc6 fragment (p49-tCdc6) that lacks the carboxy-terminal nuclear export sequence (NES). Cdc6 is known to be phosphorylated by cyclin A-Cyclin A-dependent kinase 2 (Cdk2), an event that promotes its exit from the nucleus and probably blocks it from initiating inappropriate DNA replication. (omitted)

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찔레 영지버섯(Phellinus ribis) 추출물의 생리활성 (Physiological Activities of Phellinus ribis Extracts)

  • 송재환;이현숙;황진국;정태영;홍성렬;박기문
    • 한국식품과학회지
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    • 제35권4호
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    • pp.690-695
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    • 2003
  • Phellinus ribis(찔레 영지버섯)는 약용버섯으로 일부 항암 및 관절염 치료에 사용되고 있으나 그 활성이 전혀 알려져 있지 않아 1차적으로 40% ethanol 추출물의 생리활성을 확인하였다. 항산화 활성에 있어 nitrosamine의 원인물질인 nitrite 제거활성은 pH 1.2에서 0.5 mg/mL 이하 농도에서는 50% 이하, 그리고 1 mg/mL 처리 시 $64.0{\pm}1.6%$의 제거활성을 나타냈으며, 농도 의존적으로 증가하였다. DNA 손상 및 암, 당뇨, 간경화증, 심혈관질환 등의 원인물질에 관련하여 DPPH radicals의 제거활성은 0.5 mg/mL에서 $62.5{\pm}0.3%$, 1 mg/mL 처리 시 $91.3{\pm}0.8%$로 높게 나타났다. 2.5% linoleic acid의 자동산화에 미치는 항산화 활성을 측정한 결과 0.01 mg/mL 처리 시 p<0.05 수준에서, 0.5 및 1 mg/mL에서는 p<0.001 수준에서 유의성 있게 산화를 억제하였으며, superoxide dismutase 유사활성은 $530{\pm}81\;unit/g$으로 나타났다. 그리고, 항고혈압에 관련된 angiotensin converting enzyme 저해 활성은 $12.0{\pm}1.5%$로 그 활성이 미약하였다. Human 유래 암세포에 대한 세포독성 실험결과 폐암세포인 A549의 경우 100 mg/mL 농도에서도 16%로 나타나 세포독성이 미약하였고, 자궁암 세포인 HeLa의 경우 50 mg/mL에서 45%의 효과를, 위암 세표인 AGS에서는 5 mg/mL 처리 시 24%, 50 mg/mL에서는 76%, 그리고 간암 세포주인 SK-Hep-1의 경우 50 mg/mL에서 42%의 세포독성을 나타내었다. Salmonella typhimurium TA98 및 TA100에 대한 돌연변이원성 시험결과 찔레 영지버섯 추출물은 자연복귀 집락보다 histidine revertant colony 수가 2배 이상 증가하지 않았고, 추출물의 첨가농도를 증가시켜도 histidine revertant colony 수가 증가하지 않아 돌연변이성이 없었다.

영지 균사체 분획이 일차배양 간세포 기능회복에 미치는 영향 (Effect of Ganoderma lucidum Mycelial Fractions on the Functional Recovery of Primary Cultured Hepatocytes.)

  • 박혜선;현진원;김하원;심미자;김병각
    • 한국미생물·생명공학회지
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    • 제28권4호
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    • pp.209-213
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    • 2000
  • The cultured mycelia of Ganoderma lucidum were extracted and the extract was separated into six fractions by organic solvent fractionation. The antihepatotoxic activity of all the fractions was evaluated by measuring activities of glutamic pyruvic transaminase (GPT) and glutamic oxaloacetic transaminase (GOT). Among the fractions tested, the high-polarity fractions such as aqueous and n-butanol fractions significantly reduced activities of GPT and GOT in CCl4- and galactosamine-intoxicated rat primary hepatocytes. When intracellular synthetic activities were measured by pulsing the rate primary cultured hepatocytes with [3H]-uridine and [3H]-leucine, activities of DNA, RNA and protein. When direct toxicities of the fractions were measured against human hepatoma(SK-Hep-1), the non-polarity fractions such as n-butanol and ethyl acetate fractions showed potent direct cytotoxicities even at the concentration of 1 $\mu\textrm{g}$/ml. These data showed that Ganoderma lucidum has hepatoprotective and hepatotoxic recovery principles in its mycelia.

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Protective effects of synthetic of 3-Alkoxy-6-allylthiopyridazine against aflatoxin $B_1$- induced hepatotoxicity

  • Soon, Shin-Hea;Kang, Joo-Yeon;Park, Myung-Sook;Kwon, Soon-Kyoung
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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    • pp.172.2-173
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    • 2003
  • 3-Alkoxy-6-allylthiopyridazine derivatives showed the strongest protective effect against oxidative stress and their anticancer effect determined on the growth of SK-Hep-l hepatocellular carcinomar cells. The allythio group as a pharmacologically active group was introduced into pyridazine nucleus and a substituent such as halogen or alkoxy was also introduced into paraposition of allylthio group. Five kinds of 3-alkoxy-6-allylthiopyridazine derivatives were synthesized and their chemoprotective activities examined in rats exposed to aflatoxin $B_1$-toxicant. (omitted)

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활락효영단합인삼양위탕(活絡效靈丹合人蔘養胃湯)이 혈관신생(血管新生) 억제(抑制)에 미치는 영향(影響) (Effect of Whalakyuoleyng-dan plus Yinsamyangwui-tang on Anti-angionesis)

  • 고기완;박준혁;강희;김성훈;유영법;심범상;최승훈;안규석
    • 대한한방종양학회지
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    • 제7권1호
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    • pp.77-97
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    • 2001
  • Anti-angiogenesis is one of therapies which have been high-lightened on the research of cancer treatment. Anti-angiogenesis means that new blood vessels are created from a existing capillary tube and it is a important process on metastasis and permeation when cancer is created or formed. Since angiogenesis have been under research, a complete recovery oriented treatment against cancer have been suggested blocking metastasis, delaying the growth of cancer cell, and blocking the supply of oxygen and nutritive substance through the web of blood vessels. Until now, there are several anti-angiogenesis, which have been known to the public, such as thalidomide, angiostatin, endostatin, 2-methoxyestradiol, TNP-470, and marimastat, etc. Additionally, 17 clinical testing projects about anti-angiogenesis are on the process in NCI(National Cancer Institute). Especially, TNP-470 showed effectiveness against cancer on clinical testing after finishing animal testing. Based on existing researches showing that Yinsamyangwui-tang is effective to strengthening body resistance and Whallakhyolenyng-dan effects cells on the inside of blood vessel because Whallakhyolenyng- dan restrains cell adhesion during the restraining period of a blood vessel, I tried to research the effect of Whalakhyolenyng-dan plus Yinsamyangwui-tang on angiogenesis. I made a conclusion putting into operation through using SK-Hep-1 (KCLB 30052), A549(KCLB 10185), AGS(KCLB 21739), and BCE(Bovine Capillary Endothelial Cell). Followings are the results of my experimental research: 1. According to the researching results of anti-cancer activation against cancer cell, Whallkhyoleyng dan plus Yinsamyangwui-tang decreased the number of cancer cells -- While injecting $600{\mu}g/ml$, injected groups decreased 3.1% more comparing with the contrastive group of SK-Hep-1, 49.7% more comparing with the contrastive group of A549, and 31.0% more comparing with the contrastive group of AGS. 2. According to the researching results of DNA composition effect between BCE and cancer cell, Whallakhyoleyng-dan plus Yinsamyangwui-tang reduced the rate of SK-Hep-1 synthesis inhibition by 59.1% at $600{\mu}g/ml$ intensity comparing with contrastive group; for A549, 72.6%; for AGS, 6.1%, for BCE, 28.9%. 3. According to the researching results about the effect of BCE cell to angiogenesis, angiogenesis was restrained at $400{\mu}g/ml$ intensity during 18 hours observation. 4. In the case of aortic ring assay, the half level of angiogenesis was reduced comparing with the contrastive group while injecting with $400{\mu}g/ml$ intensity; with $800{\mu}g/ml$, under 10% comparing with contrastive group; and with $1600{\mu}g/ml$, complete restrain. According to the above results, Whallakhyoleyng-dan plus Yinsamyangwui-tang was proved to have an anti-angiogenetic effects.

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Caspase-3 Specifically Cleaves $p21^{WAF1/CIP1}$ in the Earlier Stage of Apoptosis in SK-HEP-1 Human Hepatoma Cells

  • Park, Jeong-Ae;Kim, Kyu-Won;Kim, Shin-Il;Lee, Seung-Ki
    • 고려인삼학회:학술대회논문집
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    • 고려인삼학회 1998년도 Advances in Ginseng Research - Proceedings of the 7th International Symposium on Ginseng -
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    • pp.231-243
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    • 1998
  • In the present study, we provide evidence that ginsenoside $Rh_2$ (G-$Rh_2$) as well as staurosporine induces apoptosis of human hepatoma SK-HEP-1 cells by caspase 3-mediated processing of $p21^{WAFI/CIPI}$ in the early stage of apoptosls. Immunoblottings showed that G-$Rh_2$ as well as statrosporine induced the processing of caspase-3 to an active form, pl7. In stable Bcl-2 transfectants however, G-$Rh_2$ induced DNA fragmentation, while staurosporine did not. In the early stage of apoptosis, $p21^{WAFI/CIPI}$ was detected to undergo proteolytic processing specifically conducted by caspase-3. $p21^{WAFI/CIPI}$ translated in vitro was cleaved into a p14 fragment, when incubated with cell extracts obtained from either G-$Rh_2$- or staurosporine-treated cells. Cleavage was equally inhibited in both cases by adding Ac-DEVD-cho, a specific caspase-3 inhibitor, but not by Ac-YVkD-cho, a specific caspase-l inhibitor. Similarly, $p21^{WAFI/CIPI}$ was efficiently leaved by recombinant caspase-3 overexpressed in E. coli. Moreover, the endogenous $p21^{WAFI/CIPI}$ of untreated-cell extracts was also cleaved by recombinant caspase-3. Mutation analysis allowed identification of two caspase-3 cleavage sites, $DHVD^{112}$/L and $SMTD^{149}$/F, which are located within, or near the interaction domains for cyclins, Cdks, and PCNA. Taken together, these results show that G-$Rh_2$ as well as staurosporine increases caspase-3 activity, which in turn directly cleaves $p21^{WAFI/CIPI}$ resulting in elevation of Cdk kinase activity in the early stages of apoptosis. We propose that proteolytic cleavage of $p21^{WAFI/CIPI}$ is a functionally relevant event that allows unleashing the cyclin/Cdk activity from the inhibitor seen in the earlier stage of apoptosis, the event of which may be associated with the triggering mechanism for the execution of apoptosis.

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Antioxidant, Antimicrobial, and Cytotoxic Activities of Ovotransferrin from Egg White

  • Moon, Sun-Hee;Lee, Jae-Hoon;Lee, Yong-Ju;Paik, Ji-Yeon;Ahn, Dong-Uk;Paik, Hyun-Dong
    • 한국축산식품학회지
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    • 제32권5호
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    • pp.612-617
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    • 2012
  • The antioxidant, antimicrobial, and cytotoxic activities of ovotransferrin were investigated in vitro. The antioxidant capacity of ovotransferrin was evaluated using the 2,2-Diphenyl-1-picryl hydrazyl (DPPH) radical scavenging method, antimicrobial effects using the agar well diffusion method, and cytotoxicity using the 3-(4,5-dimethylthizol-2-yl)-2,5-diphenylatetetrazolium bromide (MTT) assay. The DPPH radical-scavenging capacity of ovotransferrin at 1 mg/mL level reached approximately 60% after 48 h of reaction. The antimicrobial effects of ovotransferrin against common food-borne pathogens, Staphylococcus aureus KCCM 32395, Bacillus cereus KCCM 40935, Listeria monocytogenes ATCC 15313, Escherichia coli O157:H7 ATCC 43895, and Helicobacter pylori HpKCTC 26695 were dose dependant. Gram-positive bacteria was more sensitive to ovotransferrin than gram-negative bacteria. Ovotransferrin showed stronger antimicrobial effect against L. monocytogenes than other gram-positive bacteria tested. The cytotoxicity of ovotransferrin was evaluated in human cancer cell lines, various tissue origins, including the larynx (Hep-2), stomach (AGS), lung (SK-MES-1), liver (HepG2), breast (MCF-7), cervix (HeLa), and colon (HT-29). Ovotransferrin displayed relatively high cytotoxicity (${\leq}60%$ inhibition effects) at 40 mg/mL. At lower concentrations (${\leq}10mg/mL$), however, ovotransferrin cytotoxic effects were not significant in all cancer cell lines tested. These results indicated that ovotransferrin has potential to be used as an antioxidant or antimicrobial agent in foods or a pharmaceutical agent against cancers.

세복수초(Adonis multiflora) 추출물의 항암 활성 (Anticancer Effects of the Extracts of Adonis multiflora)

  • 한효상
    • 한국자원식물학회지
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    • 제28권5호
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    • pp.561-567
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    • 2015
  • 본 연구에서는 세복수초 추출물에 대한 항암활성을 평가하고자 간암세포주인 SK-Hep1 세포주에서 MTT를 통한 세포독성을 평가하고 자가포식(autophagy) 형성정도를 확인하였다. 또한, 종양형성능 측정(Xenograft assay)를 통하여 세복수초 추출물에 대한 항암활성평가를 수행하였다. 그 결과 in vivo및 in vitro에서 모두 항암활성이 뛰어나게 나타났으며, 세복수초 추출물의 항암작용은 자가포식(autophagy)을 증가시키는 것으로 나타났다. 세복수초 추출물은 in vitro및 in vivo에서 모두 LC3의 발현을 농도의존적으로 증가시켜며 p62의 발현을 억제시키는 것으로 확인되었으며, 따라서 세복수초 추출물은 자가포식(autophagy) 활성을 증가시켜 암세포의 세포사멸을 유도하는 것으로 판단되어 간암치료제 개발 및 간암치료제와의 병용요법 등 새로운 작용기전의 항암신약개발 소재로서의 가능성이 있음을 제시한다.