References
- J. Nutrition v.129 Murphy and Lin Yan, Soybean Isoflavones Reduce Experimental Metastasis in mice Oonghua Li;John A. Yee;Michael H. McGuire;Patricia A. https://doi.org/10.1093/jn/129.5.1075
- Cold Spring Harb Symp Quant Biol v.59 Angiostatin: a circulating endothelial cell inhibitor that suppresses angiogenesis and tumor growth O'Reilly MS;Holmgren L;Shing Y;Chen C;Rosenthal RA;Cao Y;Moses M;Lane WS;Sage EH;Folkman J. https://doi.org/10.1101/SQB.1994.059.01.052
- Cell v.79 no.2 Angiostatin: a novel angiogenesis inhibitor that mediates the suppression of metastases by a Lewis lung carcinoma O'Reilly MS;Holmgren L;Shing Y;Chen C;Rosenthal RA;Moses M;Lane WS;Cao Y;Sage EH;Folkman J https://doi.org/10.1016/0092-8674(94)90187-2
- Cell v.88 no.2 Endostatin: an endogenous inhibitor of angiogenesis and tumor growth O'Reilly MS;Boehm T;Shing Y;Fukai N;Vasios G;Lane WS;Flynn E;Birkhead JR;Olsen BR;Folkman J https://doi.org/10.1016/S0092-8674(00)81848-6
- J Clin Pharmacol v.38 no.10 Regulating angiogenesis: a new therapeutic strategy Gibaldi M. https://doi.org/10.1002/j.1552-4604.1998.tb04384.x
- The Journal of Biological Chemistry v.272 no.33 Generation of Angiostatin by Reduction and Proteolsis of plasmin Paul Statihakis;Melinda Fitzgerald; Lisa J. Matthiss;Colin N. Chestermn;Philip J. Hogg https://doi.org/10.1074/jbc.272.33.20641
- Cancer Lett v.150 no.1 Antioxidant and anti-tumor promoting activities of the methanol extract of heat-processed ginseng Keum YS;Park KK;Lee JM;Chun KS, Park JH;Lee SK;Kwon H;Surh YJ https://doi.org/10.1016/S0304-3835(99)00369-9
- Biochem Pharmacol v.59 no.9 Induction of G(1) cell cycle arrest and p27(KIP1) increase by panaxydol isolated from Panax ginseng Moon J;Yu SJ;Kin HS;Sohn J https://doi.org/10.1016/S0006-2952(00)00235-5
- Jpn J Pharmcol v.49 no.3 Mechanisms of antitumor activity of aqueous extracts from Chinese herbs: their imunopharmacological properties Mori H;Xu Q;Sakamoto 0;Uesugi Y;Koda A;Nishioka I https://doi.org/10.1254/jjp.49.423
- Methods Find Exp Clin Pharmacol v.14 no.9 Shi-quan-da-bu-tang (ten significant tonic decoction), SQT. A potent Chinese biological response modifier in cancer immunotherapy, potentiation and detoxification of anticancer drugs Zee-Cheng RK
- Mutagenesis v.9 no.6 Moderate inhibition of mutagenicity and carcinogenicity of benzo[a]pyrene, 1,6-dinitropyrene and 3,9-dinitrofluoranthene by Chinese medicinal herbs Horikawa K;Mohri T;Tanaka Y;Tokiwa H https://doi.org/10.1093/mutage/9.6.523
- Zhonghua Zhong Liu Za Zhi v.16 no.6 Observation of the effects of LAKjIL-2 therapy combining with Lycium barbarum polysaccharides in the treatment of 75 cancer patients Cao GW;Yang WG;Ou P
- Int J Cancer v.70 no.6 The anti-tumor effect of Ganoderma lucid urn is mediated by cytokines released from activated macrophages and T Iymphocyes Wang SY;Hsu ML;Hsu He;tzeng CH;Lee SS;Shiao MS;Ho CJ https://doi.org/10.1002/(SICI)1097-0215(19970317)70:6<699::AID-IJC12>3.0.CO;2-5
- Thromb Res v.99 no.2 Potentiation of ganodermic acid 5 on prostaglandin E(1)-induced cyclic AMP elevation in human platelets Su C;Shiao M;Wang C https://doi.org/10.1016/S0049-3848(00)00250-4
- Mutat Res v.496 no.1-2 Antimutagenic effects of the mushroom Agaricus blazei Murrill extracts on V79 cells Menoli RC;Mantovani MS;Ribeiro LR;Speit G;Jordao BQ https://doi.org/10.1016/S1383-5718(01)00227-3
- J Biol Chem v.257 Isolation and characterization of Viscumin, a toxic lectin from Viscum album L. (mistletoe) Olsnes S;Stripe F;Sandvig K;Phil A
- Nutr Cancer v.29 no.1 Effect of dietary supplementation of soybeans on experimental metastasis of melanoma cells in mice Yan L;Yee JA;McGuire MH;Graef GL https://doi.org/10.1080/01635589709514594
- J Immunol Methods v.65 Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays Mosmann T https://doi.org/10.1016/0022-1759(83)90303-4
- Biochemical and Biopysical Research Communications v.282 HARP Induces Angiogenesis in Vivo and in vitro: Implication of N or C Terminal Peptides E. Papadimitriou;A. Polykratis;J. Courty;P. Koolwijk;M. Heroult;P. Katsoris https://doi.org/10.1006/bbrc.2001.4574
- Am J Hematol v.68 no.1 Relationships between thrombohemorrhagic complications and platelet function in patients with essential thrombocythaemia Anna Raszeja-Specht;Anna Skibowska;Maria https://doi.org/10.1002/ajh.1145
- Vaccine v.12 MDP-Lys(L18), a lipophilic derivative of muramyl dipeptide, inhibits the metastasis of haematogenous and non-haematogenous tumours in mice Yoo YC;Saiki I;Sato K;Azuma I https://doi.org/10.1016/0264-410X(94)90057-4
- Arch Pharm (Weinheim) v.333 no.6 Synthesis and evaluation of the antitumor activity of 2-substituted lA-dihydroxy-9,l0-anthraquinones Mai NT;NguyenHN;Jin GZ;Song GY;Ahn BZ https://doi.org/10.1002/1521-4184(20006)333:6<189::AID-ARDP189>3.0.CO;2-T
- Cell v.64 Cancer Metastasis and angiogenesis: An Imbalance of Positive and Negative Regulation Lance A. Liotta https://doi.org/10.1016/0092-8674(91)90642-C
- Br J Cancer v.60 no.5 Antimetastatic effects of synthetic polypeptides containing repeated structures of the cell adhesive Arg-Gly-Asp (RGD) and Tyr-Ile-Gly-Ser-Arg (YIGSR) sequence Saiki I;Murata J;Iida J;Sakurai T;Nishi N;Matsuno K;Azuma I https://doi.org/10.1038/bjc.1989.347
- Cancer Res v.42 no.6 Role of laminin in the attachment and metastasis of murine tumor cell Terraniva VP;Liotta LA;Russo RG;Martin GR
- Science v.226 no.4677 Modulation of metastatic activity of melanoma cells by laminin and fibronectin Terranova VP;Williams JE;Liotta LA;Martin GR https://doi.org/10.1126/science.6505678
- Int J Cancer v.11 no.3 Platelet-tumor-cell interactions in mice. The role of platelets in the spread of malignant disease Gasic GJ;Gasic TB;Galanti N;Johnson T;Murphy S https://doi.org/10.1002/ijc.2910110322
- Trombosis and Haemostasis v.74 Role of Platelets, Thrombin, Integrin IIb-IIIa, Fibronectin and Von Willebrand Factor on Tumor Adhesion in Vitro and Metastasis in Vivo Mary Lynn Nierodzik
- Z Krebsforsch Klin Onkol Cancer Res CIin Oncol v.86 no.3 The influence of platelet aggregation inhibitors on metastasis formation mice(3LL) Hilgard P;Heller H;Schmidt CG https://doi.org/10.1007/BF00286943
- Anticancer Res v.7 no.5 Metastases of human tumors in experimental animals Dore JF;Bailly M;Bertrand S
- Curr Opin Oncol v.3 no.1 Molecular mechanisms of cancer metastasis: tumor and host properties and the role of oncogenes and suppressor genes Nicolson GL https://doi.org/10.1097/00001622-199102000-00012
- Cell v.64 no.2 Cancer metastasis and angiogenesis: an imbalance of positive and negative regulation Liotta LA;Steeg PS;Steiler-Stevenson WG https://doi.org/10.1016/0092-8674(91)90642-C
- Eur J Clin Invest v.20 no.5 Host and tumour factors in cancer metastasis Fidler IJ https://doi.org/10.1111/j.1365-2362.1990.tb01914.x
- Zhongguo Zhong Xi Yi Jie He Za Zhi v.14 no.7 Studies of guben quyu No I combined with chemotherapy in treating cancer Yu RC;Peng XM;Rao XQ
- Planta Med v.64 no.2 Acidic polysaccharide from Panx ginseng, ginsa, induces Th1 cell and macrophage cytokines and generates LAK cells in synergy with rIL-2 Kim KH;Lee YS;Jung IS;Park SY; Chung HY;Lee IR https://doi.org/10.1055/s-2006-957385
- Int J Immunoparmacol v.11 no.6 Immunological mechanisms of ntitumor activity of some kinds of crude drugs on tumor necrosis factor production XU QA;Mori H;Sakamoto O;Uesugi Y;Koda A https://doi.org/10.1016/0192-0561(89)90145-8
- Anticancer Res v.17 no.1 Activation of multiple efector pathways of immune system by the antineoplastic immunostimulator acidic polysaccharide ginsan isolated from Panax ginseng Lee YS;Chung IS;Lee IR;Kim KH;Hing WS;Yun YS
- Biol Pharm Bull v.17 no.5 Inhibition of tumor angiogenesis and metastasis by a saponin of Panx ginseng, ginsenoside-Rb2 Sato K;Mochizuki M;Saiki I;Yoo YC;Samukawa K;Azuma I https://doi.org/10.1248/bpb.17.635
- J Nutr v.131 no.5 Isolation of an antitumor compound from Agaricus blazei Murill and its mechanism of action Takaku T;Kimura Y;Okuda H
- Jpn J Pharmacol v.48 no.1 Immunological mechanisms of antitumor activity of some kinds of Chinese herbs: Meth A-induced delayed type hypersensitivity Mori H;Xu QA;Sakamoto O;Uesugi Y;Ono Y;Koda A;Nishioka I https://doi.org/10.1254/jjp.48.37
- Eur J Cancer v.35 no.11 How Useful Unconventional cancer Treatments? Ernst E;Cassileth BR https://doi.org/10.1016/S0959-8049(99)00198-7
- Cancer Causes Control v.11 no.6 The cancer-preventive potential of Panax ginseng: a review of human and experimental evidence Shin HR;Kim JY;Yun TK;Morgan G;Vainio H https://doi.org/10.1023/A:1008980200583
- Int J Epidemiol v.27 no.3 Non-organ specific cancer prevention of ginseng: a prospective study in Korea Yun TK;Choi SY https://doi.org/10.1093/ije/27.3.359
- J. Biol. Chem. v.257 1982. Isolation and characterization of Viscumin, a toxic lectin from Viscum album L. (mistletoe). Olsnes, S.;Stripe, F.;Sandvig, K.;Phil, A.