• 한국식품과학회지
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• 제32권3호
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• pp.726-735
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• 2000

목질진흙버섯 자실체와 배양 균사체의 열수추출 및 열수 추출물의 에탄올, UF처리 분획들에 대한 약리 효과를 조사하여 다음과 같은 결과를 얻었다. Sarcoma 180 암세포 증식 저지율은 자실체 열수 총 분획(Fr. I)보다 비교적 고분자인 다당류 분획(Fr. II, Fr. III, Fr. IV)에서 $80.4{\sim}85.9%$로 높게 나타났다. 면역계에 미치는 영향으로 보체계 활성화는 $10.1{\sim}13.6%$, 대식세포의 NO 생성능은 자실체 및 균사체 모든 분획에서 생성되었으며, $TNF-{\alpha}$생성능은 NO 생성능이 높았던 분획들에서 높은 생성능을 나타내었다. 효소적 및 비효소적 지질과산화 유발에 대한 영향은 목질진흙버섯 자실체와 배양 균사체의 모든 분획에서 지질 과산화 억제능을 나타내었고, 유리기 제거능에 있어서는 농도의존적으로 효과가 있는 것으로 나타났으며, DPPH에 대한 Fr. III의 $SC_{50}$은 $32.0\;{\mu}g/mL$로 조사되었다. 상기와 같은 결과들로부터 목질진흙버섯 자실체와 배양 균사체의 열수추출 및 열수 추출물의 에탄올, UF처리 분획들은 항암활성, 면역활성, 지질 과산화 억제효과 및 유리기 제거능이 있음을 확인할 수 있었다.

• 한국약용작물학회지
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• 제18권3호
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• pp.143-150
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• 2010

This study showed the increase of antitumor activities of water soluble E. sinica extract by nano-encapsulation process with lecithin. Five groups of lecithin only group (LO), lecithin nano-encapsulated E. sinica group (LE), E. sinica only group (EO), one negative control group (NCO) and positive control group (PCO) were set for several anticancer experiment and fed into Sarcoma-180 injected mice. The cytotoxicity of LE on the human normal kidney cell (HEK293) showed 14.8% lower than 19.2% of EO and 18.4% of LO. Growth of human liver carcinoma cell and human stomach carcinoma cell as representative of digestive system in vitro was inhibited up to about 85.1% and 87.3%, in adding 1.0 mg/$m{\ell}$ of LE, which values 15% higher than that from conventional EO. The survival rates of each mice group were 40%, 63%, 48%, 33% and 100%, respectively after 40 days of injecting Sarcoma-180. The increment of their body weights of the extract feeding groups was suppressed down to 10~15%, compared to the negative control. The nano-particles also reduced the hypertrophy of the internal organs such as spleen and liver down to 15~20%, compared to those as the other groups. Among them, LE effectively reduced the size of tumor form to 20%. From these results, in vitro and in vivo antitumor activities of E. sinica could be enhanced by using nano-encapsulation process with lecithin because of better permeation into the cancer cells by confocal observations.

• 생약학회지
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• 제24권4호
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• pp.267-281
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• 1993

To find antitumor components from higher fungi, the mycelia of Collybia confluens (Pers. ex Fr.) Kummer were cultured in artificial media. For efficient production of the mycelia, the influences of various modifications of culture conditions were examined. A water-soluble protein-bound polysaccharide fraction, Fr. A, was obtained from the mycelia by hot water extraction. When Fr. A was purified and fractionated by DEAE-cellulose and Sepbadex G-200 gel filtration chromatographies into four fractions which were designated B, C, C-I and C-II. The tumor inhibition ratios of these fractions ranged from 46% to 75% against the solid forms of sarcoma 180 in ICR mice at doses of 20 and 50 mg/kg/day when given intraperitoneally. Especially, Fr. C which was named Collyban(CB) exhibited a marked life-prolonging effect of the mice against ascitic forms of sarcoma 180 at a dose of 50 mg via i.p. administration. To extend spectra of the antitumor activities and eliminate the effects of allograft rejection, the characterization of antitumor effects of CB was performed in syngeneic host-tumor systems. It did not show any antitumor activity against L1210 murine leukemia in $CD_2Fl$ mice but prolonged their life span against ascitic forms of $MM_{46}$ carcinoma in $C_3H/He$ mice. Also it exhibited antitumor activity against human cervical cancer HeLa cells that were xenografted into nude mice having BALB/c genetic backgrounds by the i.p. injection at a dose of 100 mg/kg/day. In order to characterize the antitumor components, CB was examined by chemical analysis. It was acidic protein-bound polysaccharides composed of 31% polysaccharide, 27% protein and 3% hexosamine. CB was fractionated into two fractions, Fr. C-I(M.W.: 500 Kd) and Fr. C-II(M.W.:30 and 8 Kd) by Sephadex G-200 gel filtration chromatography.

• 한국식품영양과학회지
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• 제33권3호
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• pp.475-479
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• 2004

저령 버섯으로부터 추출된 다당체는 78.2%의 당류, 16.8%의 단백질 및 4%의 회분으로 구성되었다. 저령다당체는 20-160 mg/kg/day로 ,3주간 투여 시 ICR mouse에서 유발된 sarcoma-180에 대하여 항종양효능을 나타내었다. 또한 저령다당체를 50-400$\mu\textrm{g}$/mL의 농도로 투여시 백혈암세포인 L-1210와 K-562세포에서 대조군에 비하여 52.6%, 55.0%로 각각 성장하였다. 그러나 이들 세포에서 세포사멸의 생화학적인 증거가 되는 DNA 분절현상은 나타나지 아니하였다. 2.5-10.0%의 농도의 저령다당체는 Salmonella typhimurium TA 100과 TA 98에서 2-nitrofluorene과 sodium azide에 의해 유발된 돌연변이를56%까지 억제하였다 이 결과로 저령다당체는 항종양효능, 암세포성장 억제효능 및 항돌연변이 효능을 갖는 것으로 사료되며, 이 항종양 및 암세포 성장억제효능은 세포사멸(apoptosis)에 기인하지 않는 것으로 사료된다.

• 대한한방종양학회지
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• 제3권1호
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• pp.67-84
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• 1997

Bujeonghangamtang(扶正抗癌湯) has been used for cure of tumor as a traditional medicine without any experimental evidence to support the rational basis for its clinical use. This study was carried out to evaluate the possible therapeutic or antitumoral effects of Bujeonghangamtang extract against tumor, and to carry out some mechanisms responsible for its effect. Some kinds of tumor were induced by the typical application of 3-methylcholanthrene. (MCA) or by the implantation(s.c) of malignant tumor cells such as leukemia cells(3LL cells) or sarcoma cells(Sl80 cells). Treatment of the Bujeonghangamtang water-extract (dailly 1mg／mouse, i. p.) was continued for 7 days prior to tumor induction and after that the treatment was lasted for 20 days. Against squamous cell carcinoma induced by MCA, Bujeonghangamtang decreased not only the frequency of tumor production but also the number and the weight of tumors per tumor bearing mice (TBM). Bujeonghangamtang also significantly suppressed the development of 3LL cell and S180 cell-implanted tumors in occurrence-frequency and their size, and some developed tumors were regressed by the continuous treatment of Bujeonghangamtang extract into TBM. In vitro, treatment of Bujeonghangamtang extract had no effect on the growth of some kinds of cell line such as FsaII, A431 strain but significantly inhibited the proliferation of 3LL, S180 cells and augmented the DNA synthesis of mitogen-activated lymphocytes. Bujeonghangamtang also stimulated the migrative ability of leukocyte, the MIF and IL-2 production of T lymphocytes, but not IL 6 production of B cells. Bujeonghangamtang-administration to mice enhanced NK cells activities. These results demonstrated that Bujeonghangamtang extract exhibited a significant prophylactic benefits against tumors and its antitumor activity was manifested depending on the type of tumor cells. And these results also suggested that effect of Bujeonghangamtang might be chiefly due to nonspecific enhancement of NK cell activities and cell-mediated immune responses.

• 대한한방종양학회지
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• 제6권1호
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• pp.19-28
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• 2000

In this experiment, we examined the the effect of Laetrile Oil to the immune system and tried to disclose the anti-cancer mechanism of this. The result is listed as below. 1. After per-os, sub-cutaneous and into the peritoneal injection of Laetrile Oil to the SPF mice, the LD50 is above 5000mg/kg at even group. 2. Mean survival days of mice treated with laetril oil, after S-180 cells transplantation into the peritoneal cavity decreases 1.5 days(-6.8%) compared with the Mean survival days of the control group(22days.) 3. Effects of laetril oil on natural killer cell activity at Effector/Target Cell Ratio with 100:1, 50:1, 10:1 into methotrexate-pretreated mice is like this.: Compared with $29.22\pm12.7\%$ Cytotoxicity of the control group, sample group's Cytotoxicity had $38.83{\pm}12.5%$ of meaningful acrease. At 100:1 Effecr/Target Cell Ratio. At 50:1 Effector/Target Cell Ratio, control group has $20.02{\pm}9.6%$ Cytotoxiciy and sample group had $31.53{\pm}13.4%$ Cytotoxicity. At 25:1 Effector/Target Cell Ratio control group has $13.60{\pm}6.6%$ Cytotoxicity and sample group had $20.81{\pm}9.8%$ Cytotoxicity According to the above results, the Laetrile Oil represents nontotoxic to a SPF mice. non-effective to transplantable Sarcoma 180 tumors, and activaion in NK cell activity.

• 생약학회지
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• 제17권1호
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• pp.23-34
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• 1986

To find antitumor components of Lyophyllum decastes, the mycelia of L. decastes were cultured in artificial media and a new antitumor component which showed potent antitumor activity against sarcoma 180 implanted in mice, was isolated and named 'Lyophyllan A'. Lyophyllan A was composed of a polysaccharide moiety (86%) and a protein moiety (2%). The polysaccharide moiety was found to be a heteroglycan which consisted of glucose (48.1%), mannose (30.8%), galactose, xylose and fucose. The protein moiety contained 18 amino acids. Cultural characteristics of L. decastes were investigated by shake culture method. The best result was obtained when L. decastes was cultured in medium glucose 50g, peptone 10g, corn steep liquor 30ml, $KH_2PO_4$ 0.87g, $MgSO_4$ $7H_2O$ 0.5g, $CaCl_2$ 0.3g, $FeSO_4{\cdot}7H_2O$ 10mg, $MnCl_2{\cdot}4H_2O$ 7mg, $ZnSO_4{\cdot}7H_2O$ 4mg and $CuSO_4{\cdot}5H_2O$ 1mg per one liter at $26^{circ}C$, 180rpm, for 9 days.

• Archives of Pharmacal Research
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• 제21권2호
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• pp.198-206
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• 1998

Fourty eight derivatives of 2-(1-oxyalkyl)-1,4-dioxy-9,10-anthraquinone were synthesized, and their antitumor activity was evaluated. On the whole, 2-(1-hydroxyalkyl)-1,4-dihydroxy-9,10-anthraquinones (DHAQ=1,4-dihydroxy-9,10-anthraquinone) showed stronger cytotoxic activity against L1210 cells than 2-(l-hydroxyalkyl)-1,4-dimethoxy-9,10-anthraquinones(DMAQ =1,4-dimethoxy-9,10-anthraquinone), implying that free hydroxy groups at C-1 and C-4 of the anthraquinone structure are necessary for the cytotoxic activity. The bioactivity of 2-(lhydroxyalkyl)-DHAQ derivatives differed according to the size of alkyl group at C-1;while the elongation of alkyl group over 7 carbon atoms failed to enhance the bioactivity, the derivatives possessing alkyl moiety of 1-6 carbon atoms showed an increase in the cytotoxicity and the antitumor activity in Sarcoma-180; 2-hydroxymethyl-DHAQ ($ED_{50}$, $15\mu\textrm{g}$/ml; T/C, 125%), 2-(1 -hydroxyethyl)-DHAQ($1.9{\mu}g/ml;139.2%)$;, 2-(1-hydroxypropyl)-DHAQ ($7.2{\mu}g$/ml; 135.1%), 2-(1-hydroxybutyl)-DHAQ ($10.2{\mu}g/ml; 125.3%)$, 2-(1-hydroxypentyl)-DHAQ ($23.7{\mu}g/ml; 110.1%$). and 2-(1-hydroxyhexyl)-DHAQ ($58{\mu}g/ml;108%$). Next, 2-(1-Hydroxyalkyl)-DHAQ derivatives were acetylated to produce 2-(1-acetoxyalkyl)-DHAQ analogues. Although the acetylation somewhat enhanced the cytotoxicity, but not the antitumor action. In addition, the presence of phenyl group at $C-1^{l}$ enhanced the cytotoxicity and the T/C value, compared to alkyl groups of same size; 2-(1-hydroxy-1-phenyl)-DHAQ ($ED_{50}$, $5.6{\mu}g$, T/C, 137%).

• 대한한의학방제학회지
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• 제5권1호
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• pp.147-168
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• 1997

Tish study was carried out to evaluate the possible therapeutic or antitumoral effects of Takrisodokyeum extract against tumor, and immunomodulatory effect. Some kinds of tumor were induced by the typical application of 3-methylcholanthrene (MCA) or by the implantation(s.c) of malignant tumor cells such as leukemia cells(3LL cells) or sarcoma cells(S-I80 and Fas II cells). Treatment of the Takrisodokyeum water-extract(daily 1mg mouse, i.p.) was continued for 7 days prior to tumor induction and after that the treatment was lasted for 15 days. Against squamous cell carcinoma induced by MCA, Takrisodokyeum decreased not only the frequency of tumor production but also the number and the weight of tumors per tumor bearing mice (TBM). Takrisodokyeum also significantly suppressed the development of 3LLcell and S-180 cell by frequency and their size, and some developed tumors were regressed by the continuous treatment of Takrisodokyeum extract into TBM. However, when tumor was induced by FsaII cell-implantation, the growth of implanted cells in mice was delayed by the water extract of Takrisodokyeum until day 7 and then rapid growth ensued. In vitro, treatment of Takrisodokyeum extract had no effect on the growth of some kind of cell lines such as FsaII, A-131 strain but significantly inhibited the proliferation of 3LL, S-180 cells. Takrisodokyeum also stimulated the migrative ability of leucocyte, the MIF and IL 2-production of T lymphocytes, but not IL 6 production of B cells. Takrisodokyeum enhanced Arthus reaction and DTH to sheep erythrocytes, and NK cells activities. These results demonstrated that Takrisodokyeum extract different results according to the type of tumor cells. And these results also suggested that antitumor effect of Takrisodokyeum might be chiefly due to nonspecific enhancement of NK cell activities and cell-mediated immune responses.

• 대한방사선치료학회지
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• 제15권1호
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• pp.19-27
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• 2003

I. 목적 Total Body Irradiation(TBI)와 Half Body Irradiation(HBI), Non-Hodgkin's lymphoma, E-Wing's sarcoma, lymphosarcoma, neuroblastoma 등의 특수한 경우에 넓은 광자선 조사면($40{\times}40cm2$ 이상)이 임상적으로 사용될 수 있다. 넓은 광자선 조사면의 선량분포는 매번 실제 측정 대신 좁은 광자선 조사면 (표준 SSD 100cm, 조사면의 크기 $40{\times}40cm2$ 미만)에서 얻은 측정결과를 이용하여 보정할 수 있으나, 단 순한 계산에 의한 방법만으로는 산란 방사선의 여러 가지 요인에 의한 실제 신체 각 부위의 선량 및 그 균일성을 알기는 힘들다. 본 연구에서는 치료거리 증가에 따른 넓은 광자선 조사면의 기본 parameter(PDD, TMR, Output, Sc, Sp)를 측정하고, 좁은 광자선 조사면에서 얻은 측정결과와 비교하여 그 차이를 확인해 보고 실제 적용여부를 알아보고자 한다. II. 대상 및 방법 표준 SSD 100cm에서 Multidata water phantom을 이용하여 조사면의 크기 변화에 따라 기본parameter(PDD, TMR, Output, Sc, Sp)를 측정하였다. 먼저 SSD 180cm에서(phantom이 치료실 바닥으로 수직방향) 조사면 증가에 따른 기본 parameter를 측정하였고, SSD 350cm에서(phantom이 치료실 벽면으로 수평방향이고 horizotal beam의 측정이 가능한 mylar를 가진 small water phantom을 이용) 같은 방법으로 측정하여 서로 비교해보았다. III. 결과 및 결론 SSD 180cm과 350cm에서 측정한 parameter들이 표준 선량측정 자료와 비교해서 오차범위가 실험적 오차에 있을 정도로 큰 차이가 없었음을 알 수 있었다. 정확한 자료를 얻기 위해 anthropomorphous phantom에서 선량측정을 하거나 이런 목적을 위해 특별히 고안된 unlimited phantom을 이용한 절대값을 얻을 수 있는 선량 측정이 요구된다. 부가적으로 작은 부피의 ionization chamber 사용과 넓은 조사면에 의한 cable과 stem effect를 고려해야 할 필요가 있다.