Wilkins, R. C., Kutzner, B. C., Truong, M., Sanchez-Dardon, J., & Mclean, J.

hyperlipidemia induced by poloxamer-407”, Yonsei medical journal, 51(4), pp. 504–510.

104. Zhang, X., Zhang, B., Zhang, C., Sun, G., & Sun, X. (2021), “Effect of Panax notoginseng Saponins and Major Anti-Obesity Components on Weight Loss”, Frontiers in pharmacology, 11, pp. 601751.

105. Iijima, Y., Bandow, K., Sano, M., Hino, S., Kaneko, T., Horie, N., & Sakagami, H. (2019), “In Vitro Assessment of Antitumor Potential and Combination Effect of Classical and Molecular-targeted Anticancer Drugs”, Anticancer research, 39(12), pp. 6673–6684.

106. Kapałczyńska, M., Kolenda, T., Przybyła, W., Zajączkowska, M., Teresiak, A., Filas, V., Ibbs, M., Bliźniak, R., Łuczewski, Ł., & Lamperska, K. (2018), “2D and 3D cell cultures - a comparison of different types of cancer cell cultures”, Archives of medical science : AMS, 14(4), pp. 910–919.

107. Obeng E. (2021), “Apoptosis (programmed cell death) and its signals - A review”, Brazilian journal of biology = Revista brasleira de biologia, 81(4), pp. 1133–1143.

108. Wilkins, R. C., Kutzner, B. C., Truong, M., Sanchez-Dardon, J., & McLean, J.

R. (2002), “Analysis of radiation-induced apoptosis in human lymphocytes: flow cytometry using Annexin V and propidium iodide versus the neutral comet assay”, Cytometry, 48(1), pp. 14–19.

109. Shoshan-Barmatz, V., De, S., & Meir, A. (2017), “The Mitochondrial Voltage-Dependent Anion Channel 1, Ca2+ Transport, Apoptosis, and Their Regulation”, Frontiers in oncology, 7, pp. 60.

110. Nichani, K., Li, J., Suzuki, M., & Houston, J. P. (2020), “Evaluation of Caspase-3 Activity During Apoptosis with Fluorescence Lifetime-Based Cytometry

Measurements and Phasor Analyses”, CytometryPart A : the journal of the International Society for Analytical Cytology, 97(12), pp. 1265–1275.

Có thể bạn quan tâm!

• Về Kết Quả Đánh Giá Độc Tính Của Cao Định Lượng Np(H).
• Đỗ Tất Lợi (2019), Những Cây Thuốc Và Vị Thuốc Việt Nam (Tái Bản Lần Thứ 20),
• Wei, G., Dong, L., Yang, J., Zhang, L., Xu, J., Yang, F., Cheng, R., Xu, R., & Chen, S. (2018), “Integrated Metabolomic And Transcriptomic Analyses Revealed The
• Nghiên cứu tác dụng kháng u thực nghiệm của rễ củ Tam thất Panax notoginseng Burk. F.H. Chen, Araliaceae trồng ở Việt Nam trước và sau chế biến - 26
• Nghiên cứu tác dụng kháng u thực nghiệm của rễ củ Tam thất Panax notoginseng Burk. F.H. Chen, Araliaceae trồng ở Việt Nam trước và sau chế biến - 27

Xem toàn bộ 222 trang tài liệu này.

111. Khan, Saleem & Telang, Avinash & Kumar, Jitendra. (2013), “DNA fragmentation, apoptosis and cell cycle arrest induced by sodium arsenite in cultured murine Sertoli cells: Prevention by curcumin”, Toxicological and Environmental Chemistry, 95(6), pp. 1006-1018.

112. Onaciu, A., Munteanu, R., Munteanu, V. C., Gulei, D., Raduly, L., Feder, R. I., Pirlog, R., Atanasov, A. G., Korban, S. S., Irimie, A.,& Berindan-Neagoe, I. (2020), “Spontaneous and Induced Animal Models for Cancer Research”, Diagnostics (Basel, Switzerland), 10(9), pp. 660.

113. Li, Z., Zheng, W., Wang, H., Cheng, Y., Fang, Y., Wu, F., Sun, G., Sun, G., Lv, C., & Hui, B. (2021), “Application of Animal Models in Cancer Research: Recent Progress and Future Prospects”, Cancer management and research, 13, pp. 2455–2475.

114. Pelleitier, M., & Montplaisir, S. (1975), “The nude mouse: a model of deficient T-cell function”, Methods and achievements in experimental pathology, 7, pp. 149–166.

115. Zhou S, Jiang N, Zhang M, Xiao X, Liu Z, Xu X, Gao Q, Lv W (2020), “Analyzing Active Constituents and Optimal Steaming Conditions Related to the Hematopoietic Effect of Steamed Panax notoginseng by Network Pharmacology Coupled with Response Surface Methodology”, BioMed Research International, 2020, pp. 9371426.

116. Wang Dong, Peng-Ying Liao, Hong-Tao Zhu, Ke-Ke Chen, Min Xu, Ying- Jun Zhang, Chong-Ren Yang (2012), "The processing of Panax notoginseng and the transformation of its saponin components", Food Chemistry, 132(4), pp. 1808- 1813.

117. Monks, A., Scudiero, D., Skehan, P., Shoemaker, R., Paull, K., Vistica, D., Hose, C., Langley, J., Cronise, P., & Vaigro-Wolff, A. (1991), “Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines”, Journal of the National Cancer Institute, 83(11), pp. 757–766.

118. Kopper L, Van Hanh T, Lapis K. (1982), “Experimental model for liver metastasis formation using Lewis lung tumor”, J Cancer Res Clin Oncol, 103(1), pp. 31-38.

119. Bagley RG, Ren Y, Kurtzberg L, Weber W, Bangari D, Brondyk W, Teicher BA (2012), “Human choriocarcinomas: placental growth factor-dependent preclinical tumor models”, Int J Oncol, 40(2), pp. 479-486.

120. Itokawa H, Ichihara Y, Watanabe K, Takeya K (1989), “An antitumor principle from Euphorbia lathyris”, Planta Med, 55(3), pp. 271-272.

121. Stefanova, T. H., Nikolova, N. J., Toshkova, R. A., & Neychev, H. O. (2007), “Antitumor and immunomodulatory effect of coumarin and 7-hydroxycoumarin against Sarcoma 180 in mice”, Journal of experimental therapeutics & oncology, 6(2), pp. 107–115.

122. Janet Hoff. (2000), “Methods of blood collection in the mouse”, Lab Animal, 29(10), pp. 47-53.

123. Geran RI, Greenberg NH, MacDonald MM, Schumacher A, Abbott BJ (1972), “Protocols for screening chemical agents and natural products against animal tumors and other biological systems”, Cancer Chemother Rep, 3(2), pp. 1- 103.

124. Bộ y tế (2015), Hướng dẫn thử nghiệm tiền lâm sàng và lâm sàng thuốc đông y, thuốc từ dược liệu, ban hành kèm theo Quyết định số 141/QĐ-K2ĐT ngày 27/10/2015 của Cục Khoa học Công nghệ và Đào tạo, Bộ y tế.

125. WHO (2000), General Guidelines for Methodologies on Research and Evaluation of Traditional Medicine.

126. Kim D. S., Y. J. Chang, U. Zedk, P. Zhao, Y. Q. Liu, C. R. Yang (1995), "Dammarane saponins from Panax ginseng", Phytochemistry, 40(5), pp. 1493-7.

127. Yahara Shoji, Kiyoko Kaji, Osamu Tanaka (1979), "Further Study on Dammarane-Type Saponins of Roots, Leaves, Flower-Buds, and Fruits of Panax ginseng C. A. Meyer", Chemical & Pharmaceutical Bulletin, 27(1), pp. 88-92.

128. Hương Trần Thu, Lê Huyền Trâm, Trần Thượng Quảng, Trần Thị Minh, Nguyễn Tuấn Anh, Hồ Đức Cường (2009), "Ginsenosid Rg1 và L-Tryptophan từ cây Lược vàng (Callisia fragrans)", Tạp chí Khoa học và Công nghệ các trường Đại học Kỹ thuật, 74, pp. 107-112.

129. Kang Dong Il, Ki-Woong Jung, Seoungkeum Kim, Sung-Ah Lee, Gil-Ja Jhon, Yangmee Kim (2007), "Tertiary structure of ginsenoside Re studied by NMR spectroscopy", Bull. Korean Chem., 28(12), pp. 2209-2213.

130. Han M., J. G. Hou, C. M. Dong, W. Li, H. L. Yu, Y. N. Zheng, L. Chen (2010), "Isolation, synthesis and structures of ginsenoside derivatives and their anti-tumor bioactivity", Molecules, 15(1), pp. 399-406.

131. Cho Jin-Gyeong, Min-Kyung Lee, Jae-Woong Lee, Hee-Jung Park, Dae- Young Lee, Youn-Hyung Lee, Deok-Chun Yang, Nam-In Baek (2010), "Physicochemical Characterization and NMR assignments of ginsenosids Rb1, Rb2, Rc, and Rd isolated from Panax ginseng", J. Ginseng Res, 34(2), pp. 113-121.

132. Li Gang, Xiao-xiao Zhang, Lin Lin, Xiao-ning Liu, Cheng-jun Ma, Ji Li, Chi- bo Wang (2014), "Preparation of ginsenosid Rg3 and protection against H2O2- induced oxidative stress in human neuroblastoma SK-N-SH cells", Journal of Chemistry, 2014, pp. 6.

133. Reuter, S., Gupta, S.C., Chaturvedi, M.M. and Aggarwal, B.B. (2010), “Oxidative stress, inflammation, and cancer: how are they linked?”, Free Radical Biology and Medicine, 49(11), pp. 1603-1616.

134. Senthilkumar, N., Badami, S., Dongre, S.H. and Bhojraj, S.(2008), “Antioxidant and hepatoprotective activity of the methanol extract of Careya arborea bark in Ehrlich ascites carcinoma-bearing mice”, Journal of Natural Medicines, 62(3), pp. 336-339.

135. Ge Feng, Zhuangjia Huang, Hong Yu, Yan Wang, Diqiu Liu (2016), "Transformation of Panax notoginseng saponins by steaming and Trichoderma longibrachiatum", Biotechnology & Biotechnological Equipment, 30(1), pp. 165- 172.

136. Lau A. J., D. F. Toh, T. K. Chua, Y. K. Pang, S. O. Woo, H. L. Koh (2009), "Antiplatelet and anticoagulant effects of Panax notoginseng: comparison of raw and steamed Panax notoginseng with Panax ginseng and Panax quinquefolium", J Ethnopharmacol, 125(3), pp. 380-6.

137. Gu CZ, Qiao YJ, Wang D, Zhu HT, Yang CR, Xu M, Zhang YJ (2018), “New triterpenoid saponins from the steaming treated roots of Panax notoginseng”, Nat Prod Res, 32(3), pp. 294-301.

138. He F, Ding Y, Liang C, Song S B, Dou DQ. Song GY, Kim YH (2014), “Antitumor effects of dammarane-type saponins from steamed Notoginseng”, Pharmacogn Mag, 10(39), pp. 314-317.

139. Kim, S. J., & Kim, A. K. (2015), “Anti-breast cancer activity of Fine Black ginseng (Panax ginseng Meyer) and ginsenoside Rg5”, Journal of ginseng research, 39(2), pp. 125–134.

140. Wang, C. Z., Aung, H. H., Ni, M., Wu, J. A., Tong, R., Wicks, S., He, T. C., & Yuan, C. S. (2007), “Red American ginseng: ginsenoside constituents and antiproliferative activities of heat-processed Panax quinquefolius roots”, Planta medica, 73(7), pp. 669–674.

141. Wang, C. Z., Anderson, S., DU, W., He, T. C., & Yuan, C. S. (2016), “Red ginseng and cancer treatment”, Chinese journal of natural medicines, 14(1), pp. 7– 16.

142. Le, T. H., Lee, S. Y., Lee, G. J., Nguyen, N. K., Park, J. H., & Nguyen, M. D. (2015), “Effects of steaming on saponin compositions and antiproliferative activity of Vietnamese ginseng”, Journal of ginseng research, 39(3), pp. 274–278.

143. Dong T. T., X. M. Cui, Z. H. Song, K. J. Zhao, Z. N. Ji, C. K. Lo, K. W. Tsim (2003), “Chemical assessment of roots of Panax notoginseng in China: regional and seasonal variations in its active constituents”, JAgric Food Chem, 51(16), pp. 4617-23.

144. J.Guan, C.M.Lai, S.P.Li, (2007), “A rapid method for the simultaneous determination of 11 saponins in Panax notoginseng using ultra performance liquid chromatography”, Journal of Pharmaceutical and Biomedical Analysis, 44(4), pp. 996-1000.

145. Wang Dong, Hwee-Ling Koh, Yan Hong, Hong-Tao Zhu, Min Xu, Ying- JunZhang, Chong-Ren Yang (2013),“Chemical and morphological variations of Panax notoginseng and their relationship”,Phytochemistry, 93, pp. 88-95.

146. J.B.Wan, C.M.Lai, S.P.Li, M.Y.Lee, L.Y.Kong, Y.T.Wang, (2006), “Simultaneous determination of nine saponins from Panax notoginseng using HPLC and pressurized liquid extraction”, Journal of Pharmaceutical and Biomedical Analysis, 41(1), pp. 274-279

147. A. J. Lau, B. H. Seo, S. O. Woo, H. L. Koh (2004), “High-performance liquid chromatographic method with quantitative comparisons of whole chromatograms of raw and steamed Panax notoginseng”, Journal of Chromatography A, 1057(1- 2), pp. 141-149.

148. Park E.H., Kim Y.J., Yamabe N., Park S.H., Kim H.K., Jang H.J., Kim J.H., Cheon G.J., Ham J., Kang K.S (2014), “Stereospecific anticancer effects of

ginsenoside Rg3 epimers isolated from heat-processed American ginseng on human gastric cancer cell”, J Ginseng Res, 38, pp. 22–27.

149. Yuan H.D., Quan H.Y., Zhang Y., Kim S.H., Chung S.H (2010), “20(S)- Ginsenoside Rg3-induced apoptosis in HT-29 colon cancer cells is associated with AMPK signaling pathway”, Mol Med Rep, 3, pp. 825.

150. Fei Z., Li M., Wu X., Hu Y., Yang C., Wang X.A., Xiang S., Li H., Lin J., Tan Z (2015), “20(S)-ginsenoside Rg3 promotes senescence and apoptosis in gallbladder cancer cells via the p53 pathway”, Drug Des Dev Ther, 9, pp. 3969– 3987.

151. Jian J., Hu Z.F., Huang Y (2009), “Effect of ginsenoside Rg3 on Pim-3 and Bad proteins in human pancreatic cancer cell line PANC-1”, Ai zheng Chinese J Cancer, 28, pp. 461.

152. Choi Y.J., Kang L.J., Lee S.G (2014), “Stimulation of DDX3 expression by ginsenoside Rg3 through the Akt/p53 pathway activates the innate immune response via TBK1/IKKε/IRF3 signalling”, Curr Med Chem, 21, pp. 1050.

153. Tang Y.C., Zhang Y., Zhou J., Zhi Q., Wu M.Y., Gong F.R., Shen M., Liu L., Tao M., Shen B (2018), “Ginsenoside Rg3 targets cancer stem cells and tumor angiogenesis to inhibit colorectal cancer progression in vivo.”, Int J Oncol, 52, pp. 127–138.

154. Lyu, X., Xu, X., Song, A., Guo, J., Zhang, Y., & Zhang, Y. (2019), “Ginsenoside Rh1 inhibits colorectal cancer cell migration and invasion in vitro and tumor growth in vivo”, Oncology letters, 18(4), pp. 4160–4166.

155. Huynh, D., Jin, Y., Myung, C. S., & Heo, K. S. (2021), “Ginsenoside Rh1 Induces MCF-7 Cell Apoptosis and Autophagic Cell Death through ROS-Mediated Akt Signaling”, Cancers, 13(8), pp. 1892.

156. Jin, Y., Huynh, D., & Heo, K. S. (2022), “Ginsenoside Rh1 inhibits tumor growth in MDA-MB-231 breast cancer cells via mitochondrial ROS and ER stress- mediated signaling pathway”, Archives of pharmacal research, 45(3), pp. 174–184.

157. Jin, Yujin, Diem T.N. Huynh, Chang-Seon Myung, and Kyung-Sun Heo (2021), "Ginsenoside Rh1 Prevents Migration and Invasion through Mitochondrial ROS-Mediated Inhibition of STAT3/NF-κB Signaling in MDA-MB-231 Cells", International Journal of Molecular Sciences, 22(19), pp. 10458.

158. Carneiro BA, El-Deiry WS (2020), “Targeting apoptosis in cancer therapy”,

Clinical Oncology, 17(7), pp. 395-417.

159. Safarzadeh E, Sandoghchian Shotorbani S, Baradaran B (2014), “Herbal Medicine as Inducers of Apoptosis in Cancer Treatment”, Advanced Pharmaceutical Bulletin, 4(5), pp. 421-427.

160. Lawal R., Ozaslan M (2021), “Effect of medicinal plants on Ehrlich ascites carcinoma cells (a review)”, Zeugma Biological Science, 2(2), pp. 19-27.

161. Bernardes, T. , Beserra, H. , Vexenat, S. , Langoni, H. and Rocha, N. (2015), “Phenotypic Characterization Murine Sarcoma TG-180 Immunophenotypical Characterization Murine Sarcoma TG-180”, Open Journal of Pathology, 5, pp. 59- 64.

162. Fang, Jun & Gao, Shanghui & Islam, Rayhanul & Teramoto, Yuji & Maeda, Hiroshi (2020), “Extracts of Phellinus linteus, Bamboo (Sasa senanensis) Leaf and Chaga Mushroom (Inonotus obliquus) Exhibit Antitumor Activity through Activating Innate Immunity”, Nutrients, 12(8), pp. 2279.

163. Jiang, Z., Abu, R., Isaka, S., Nakazono, S., Ueno, M., Okimura, T., Yamaguchi, K., & Oda, T. (2014), “Inhibitory effect of orally-administered sulfated polysaccharide ascophyllan isolated from ascophyllum nodosum on the growth of sarcoma-180 solid tumor in mice”, Anticancer research, 34(4), pp. 1663–1671.