Relevant bibliographies by topics / Ehrlich’s ascites tumour

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  1. Journal articles
  2. Dissertations / Theses
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  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Ehrlich’s ascites tumour'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Ehrlich’s ascites tumour"

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Sharmila K.P., Shilpa S. Shetty, Suchetha Kumari, Madhyastha Harishkumar, Ashwini Prabhu, and Satheesh Kumar Bhandary B. "Oroxylum indicum stem bark extract exerts antitumor potential against Ehrlich’s ascites carcinoma in Swiss albino mice." Biomedicine 42, no. 4 (2022): 686–92. http://dx.doi.org/10.51248/.v42i4.1559.

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Introduction and Aim: Constant efforts are exerted to explore unique bioactive principles from natural sources that possess more effective and specific antineoplastic activities. In the present study, we aimed to evaluate the antitumor activity of stem bark extract of Oroxylum indicum in mice bearing Ehrlich ascites carcinoma (EAC). Materials and Methods: Ninety female Swiss albino mice were categorized into fifteen groups (n=6). The animals were inoculated with 1x106 EAC cells. Tumor control animals received sterile water once daily for 10 consecutive days. Positive control group was injected
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Popov, Alexander, Anna Klimovich, Olga Styshova, et al. "Probable Mechanisms of Doxorubicin Antitumor Activity Enhancement by Ginsenoside Rh2." Molecules 27, no. 3 (2022): 628. http://dx.doi.org/10.3390/molecules27030628.

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Ginsenoside Rh2 increases the efficacy of doxorubicin (DOX) treatment in murine models of solid and ascites Ehrlich’s adenocarcinoma. In a solid tumor model (treatment commencing 7 days after inoculation), DOX + Rh2 co-treatment was significantly more efficacious than DOX alone. If treatment was started 24 h after inoculation, the inhibition of tumor growth of a solid tumor for the DOX + Rh2 co-treatment group was complete. Furthermore, survival in the ascites model was dramatically higher for the DOX + Rh2 co-treatment group than for DOX alone. Mechanisms underlying the combined DOX and Rh2 e
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Starkov, A. K., and N. M. Titova. "Targeted delivery of cisplatin conjugates with arabinogalactan to tumor using aptamers." Siberian Medical Review, no. 5 (2022): 107. http://dx.doi.org/10.20333/25000136-2022-5-107.

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The effectiveness of targeted delivery of cisplatin conjugate with arabinogalactan to ascitic Ehrlich carcinoma in vivo using the target ligand, the AS42 aptamer, was studied in this work. Studies conducted on male ICR mice with ascitic Ehrlich carcinoma. Antitumor therapy was carried out with cisplatin and an arabinogalactan-platinum complex (AG-Pt) and an AG-Pt complex modified with aptamers to ascitic Ehrlich carcinoma cells. The toxicity of drugs was determined on the basis of biochemical parameters of blood in healthy mice after 5-fold administration. In our studies, cisplatin treatment o
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Wojciak, E., and W. Korohoda. "Ehrlich ascites tumour cells show tissue-specific adherence and modify their shape upon contact with embryonic fibroblasts and myotubes." Journal of Cell Science 97, no. 3 (1990): 433–38. http://dx.doi.org/10.1242/jcs.97.3.433.

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Adhesiveness of Ehrlich ascites tumour (EAT) cells to glass, to mouse peritoneal membrane, living and aldehyde-fixed mouse embryo fibroblasts and chick embryo fibroblasts, myoblasts and myotubes was investigated. The ascitic EAT cells (and leukaemia L1210 cells) did not adhere to glass and peritoneum but readily adhered to embryo fibroblasts, myoblasts and myotubes. The attachment was followed by cell spreading and migration. Fixation of fibroblasts or myogenic cells with aldehydes did not prevent ascitic cells from attaching but reduced the rate of spreading. Only direct interaction of asciti
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Zamay, S. S., V. S. Prokopenko, K. A. Lukyanenko, and A. E. Sokolov. "Nanoscalpel based on magnetic discs and aptamers effectively and targeted destroy tumor cell." Siberian Medical Review, no. 2 (2021): 79–82. http://dx.doi.org/10.20333/25000136-2021-2-79-82.

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The aim of the research. To investigate the antitumor effi cacy of three-layer magnetic nanodiscs (Au / Ni / Au) with a quasi-dipole structure, functionalized with biorecognizing molecules of a tumor. Material and methods. Th ree-layer magnetic nanodiscs (Au / Ni / Au) 500 nm in size (were obtained by micro- and nanoelectronic technologies. Aptamers to ascites cells of Ehrlich carcinoma were used to functionalize magnetic nanodiscs. Th iol groups were used to bind disks to aptamers. As a model of tumor cells Ehrlich’s ascites carcinoma cells were used, and the cells were magnetically infl uenc
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KunduSen, Sriparna, Malaya Gupta, Upal K. Mazumder, Pallab K. Haldar, Prerona Saha, and Asis Bala. "Antitumor Activity of Citrus maxima (Burm.) Merr. Leaves in Ehrlich's Ascites Carcinoma Cell-Treated Mice." ISRN Pharmacology 2011 (April 19, 2011): 1–4. http://dx.doi.org/10.5402/2011/138737.

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Context. The plant Citrus maxima Merr. (Rutaceae), commonly known as shaddock or pomelo is indigenous to tropical parts of Asia. The objective of present study is to evaluate the methanol extract of Citrus maxima leaves for its antitumor activity against Ehrlich's Ascites Carcinoma cell in Swiss albino mice. Experimental design. The antitumor activity of methanol extract of Citrus maxima leaves (MECM) was evaluated against Ehrlich Ascites Carcinoma (EAC) cell line in Swiss albino mice. 2 × 106 cells were inoculated in different groups of animals. MECM (200 and 400 mg/kg BW i.p.) was administer
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LOBO, Carolina, Miguel A. RUIZ-BELLIDO, Juan C. ALEDO, Javier MÁRQUEZ, Ignacio NÚÑEZ DE CASTRO, and Francisco J. ALONSO. "Inhibition of glutaminase expression by antisense mRNA decreases growth and tumourigenicity of tumour cells." Biochemical Journal 348, no. 2 (2000): 257–61. http://dx.doi.org/10.1042/bj3480257.

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Phosphate-activated glutaminase has a critical role in tumours and rapidly dividing cells and its activity is correlated with malignancy. Ehrlich ascites tumour cells transfected with the pcDNA3 vector containing an antisense segment (0.28 kb) of rat kidney glutaminase showed impairment in the growth rate and plating efficiency, as well as a shortage in the glutaminase protein and activity. The C-terminal segment used is well conserved in all glutaminase sequences known. The transfected cells, named 0.28AS-2, displayed remarkable changes in their morphology compared with the parental cell line
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SALGADO, Flávio L. L., Ricardo ARTIGIANI-NETO, and Gaspar de Jesus LOPES-FILHO. "GROWTH FACTORS AND COX2 IN WOUND HEALING: AN EXPERIMENTAL STUDY WITH EHRLICH TUMORS." ABCD. Arquivos Brasileiros de Cirurgia Digestiva (São Paulo) 29, no. 4 (2016): 223–26. http://dx.doi.org/10.1590/0102-6720201600040003.

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ABSTRACT Background: Healing is an innate biological phenomenon, and carcinogenesis acquired, but with common humoral and cellular elements. Carcinogenesis interferes negatively in healing. Aim: To evaluate the histological changes in laparotomy scars of healthy Balb/c mice and with an Ehrlich tumor in its various forms of presentation. Methods: Fifty-four mice were divided into three groups of 18 animals. First group was the control; the second had Ehrlich tumor with ascites; and the third had the subcutaneous form of this tumor. Seven days after tumor inoculation, all 54 mice were submitted
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Rudel, Alena E., Tatiana A. Filatenkova, and Maria S. Zharkova. "Activity of protegrin-1 against mouse Ehrlich ascites carcinoma <i>in vitro</i> and <i>in vivo</i>." Medical academic journal 24, no. 2 (2024): 117–24. http://dx.doi.org/10.17816/maj631421.

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BACKGROUND: The problem of multidrug resistance in cancer treatment creates an urgent demand for developing new effective antitumor agents. Due to the unusual mechanism of recognizing and damaging tumor cells, antimicrobial peptides are considered as possible prototypes for designing such therapeutics. AIM: This work was aimed to compare the antitumor potential of the promising membranolytic antimicrobial peptide protegrin-1 in vitro and in vivo in Ehrlich ascites carcinoma mice model. MATERIALS AND METHODS: We used two variants of the model by inducing a tumor in solid or ascites form. In the
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Jaganathan, Saravana Kumar, Dilip Mondhe, Z. A. Wani, Harish C. Pal, and Mahitosh Mandal. "Effect of Honey and Eugenol on Ehrlich Ascites and Solid Carcinoma." Journal of Biomedicine and Biotechnology 2010 (2010): 1–5. http://dx.doi.org/10.1155/2010/989163.

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Ehrlich ascites carcinoma is a spontaneous murine mammary adenocarcinoma adapted to ascites form and carried in outbred mice by serial intraperitoneal (i/p) passages. The previous work from our laboratory showed that honey having higher phenolic content was potent in inhibiting colon cancer cell proliferation. In this work, we extended our research to screen the antitumor activity of two selected honey samples and eugenol (one of the phenolic constituents of honey) against murine Ehrlich ascites and solid carcinoma models. Honey containing higher phenolic content was found to significantly inh
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Dissertations / Theses on the topic "Ehrlich’s ascites tumour"

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Gentile, Luciana Boffoni [UNESP]. "Modulação por PGE Ind.3 no perfil de subpopulações celulares e citocinas na evolução do Tumor Ascítico de Ehrlich (TAE)." Universidade Estadual Paulista (UNESP), 2001. http://hdl.handle.net/11449/95915.

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Made available in DSpace on 2014-06-11T19:27:57Z (GMT). No. of bitstreams: 0 Previous issue date: 2001Bitstream added on 2014-06-13T20:36:40Z : No. of bitstreams: 1 gentile_lb_me_botfm.pdf: 247842 bytes, checksum: 63ea41194545ec6eec4411a86ab5ea15 (MD5)<br>Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)<br>O presente trabalho objetivou avaliar o envolvimento das prostaglandinas no crescimento tumoral, influxo inflamatório e secreação de citocinas durante a evolução do Tumor Ascítico de Ehrlich (TAE). Para tanto, camundongos foram inoculados com 1 x 103 células tumorais (ip) e tr
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Gentile, Luciana Boffoni. "Modulação por PGE Ind.3 no perfil de subpopulações celulares e citocinas na evolução do Tumor Ascítico de Ehrlich (TAE) /." Botucatu : [s.n.], 2001. http://hdl.handle.net/11449/95915.

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Orientador: Denise Fecchio<br>Resumo: O presente trabalho objetivou avaliar o envolvimento das prostaglandinas no crescimento tumoral, influxo inflamatório e secreação de citocinas durante a evolução do Tumor Ascítico de Ehrlich (TAE). Para tanto, camundongos foram inoculados com 1 x 103 células tumorais (ip) e tratados com indometacina (1mg/Kg,1x/dia,ip) ou com diluente (0,1 ml,1x/dia,ip). Decorridos 1, 3, 6, 10 e 13 dias os animais foram sacrificados e avaliados quanto ao influxo inflamatório diferencial, secreção de TNF-a, IL1-a, IL-2, IL- 4, IL-6, IL-10 e IL-13 e níveis de PGE2 no lavado p
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Mangueira, Vivianne Mendes. "Estudo da toxicidade e atividade antitumoral do derivado acridínico n’-(2-cloro-6-metoxi-acridin-9-yl)-2-ciano-3-(4-dimetilaminofenil)-acrilohidrazida em modelo experimental de tumor ascítico de ehrlich." Universidade Federal da Paraíba, 2015. http://tede.biblioteca.ufpb.br:8080/handle/tede/8821.

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Submitted by Cristhiane Guerra (cristhiane.guerra@gmail.com) on 2017-02-03T14:26:05Z No. of bitstreams: 1 arquivototal.pdf: 1920368 bytes, checksum: a0cab7d082218cd820a2d1c4f4b184f7 (MD5)<br>Made available in DSpace on 2017-02-03T14:26:05Z (GMT). No. of bitstreams: 1 arquivototal.pdf: 1920368 bytes, checksum: a0cab7d082218cd820a2d1c4f4b184f7 (MD5) Previous issue date: 2015-02-27<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES<br>Cancer is a major public health problem worldwide and is considered a group of diseases characterized by uncontrolled growth and multiplicatio
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Carvalho, Flávio Silva de. "Avaliação farmacológica e toxicológica de novos candidatos a protótipos de fármacos antitumorais." Universidade Federal de Goiás, 2011. http://repositorio.bc.ufg.br/tede/handle/tede/3273.

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Submitted by Jaqueline Silva (jtas29@gmail.com) on 2014-10-03T21:14:43Z No. of bitstreams: 2 Dissertação - Flávio Silva de Carvalho - 2011.pdf: 2542668 bytes, checksum: 8b150260143e835293c132099b3cbf68 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5)<br>Approved for entry into archive by Jaqueline Silva (jtas29@gmail.com) on 2014-10-03T21:14:50Z (GMT) No. of bitstreams: 2 Dissertação - Flávio Silva de Carvalho - 2011.pdf: 2542668 bytes, checksum: 8b150260143e835293c132099b3cbf68 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5)<br>
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Oliveira, Ana Paula Adry de. "Potencial metastático e reconhecimento da E-selectina em culturas e em tecidos colonizados pelo tumor ascítico de Ehrlich." Universidade Federal de Viçosa, 2005. http://locus.ufv.br/handle/123456789/5000.

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Made available in DSpace on 2015-03-26T13:46:45Z (GMT). No. of bitstreams: 1 texto completo.pdf: 6062546 bytes, checksum: 89becf9f70310d9f17ce56006e3de46e (MD5) Previous issue date: 2005-02-03<br>The ojective of this study was to evaluate the involvement of the adhesion molecule E-selectin in the process of metastasis of the Ehrlich ascitic tumor (EAT) and to clarify some aspects related to the invasive potential, inflammation and cellular adhesion. BALB/c mice were inoculated with 2 x 106 of the Ehrlich ascitic tumor cells by intramuscular or endovenous route, and also subcutaneous in the f
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Hamasato, Eduardo Kenji. "A influência da convivência com um parceiro doente sobre a resposta inflamatória alérgica pulmonar em camundongos." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/10/10133/tde-29092016-103925/.

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As relações bidirecionais entre o Sistema Nervoso e o Sistema Imune são relevantes para a manutenção da homeostase do organismo. Estudos realizados em nosso laboratório mostraram que 14 dias de coabitação com um conspecífico doente (injetado com células do tumor de Ehrlich-TAE) produziu mudanças comportamentais, endócrinas e imunológicas. Este estudo analisa os efeitos da convivência com um animal portador de tumor de Ehrlich em camundongos OVA sensibilizados e desafiados sobre a resposta alérgica pulmonar. Pares de camundongos machos foram separados em três grupos: naïve, controle e experimen
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Ramos, Aline Lisie. "Atividade imunomoduladora da alga Chlorella vulgaris em camundongos portadores de tumos ascitico de Ehrlich." [s.n.], 2008. http://repositorio.unicamp.br/jspui/handle/REPOSIP/311283.

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Orientador: Mary Luci de Souza Queiroz<br>Tese ( doutorado) - Universidade Estadual de Campinas, Faculdade de Ciencias Medicas<br>Made available in DSpace on 2018-08-12T11:14:50Z (GMT). No. of bitstreams: 1 Ramos_AlineLisie_D.pdf: 13996403 bytes, checksum: 20b3e94e609f9ce6fd4214680378bb52 (MD5) Previous issue date: 2008<br>Resumo: A Chlorella vulgaris (CV) é uma alga microscópica bastante rica em nutrientes. Além de alto valor nutritivo, a Chlorella tem demonstrado possuir importantes atividades terapêuticas. Vários trabalhos do nosso laboratório e outros demonstram os efeitos protetores des
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ANDRADE, Wanessa Machado. "Investigação da atividade antitumoral in vitro e in vivo da Eugenia dysenterica DC. (MYRTACEAE)." Universidade Federal de Goiás, 2011. http://repositorio.bc.ufg.br/tede/handle/tde/2115.

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Made available in DSpace on 2014-07-29T16:11:51Z (GMT). No. of bitstreams: 1 Dissertacao - Wanessa Machado Andrade - 2011.pdf: 1952980 bytes, checksum: e95aa49d2fb71af8883a1b476f7d219a (MD5) Previous issue date: 2011-08-30<br>Na busca por novos agentes antineoplásicos os produtos de origem natural têm um papel de destaque, uma vez que cerca de 25% dos fármacos prescritos no mundo são obtidos de plantas e aproximadamente 49% dos fármacos desenvolvidos nas últimas três década foram obtidos a partir de produtos naturais. Eugenia dysenterica DC. pertence à família Myrtaceae e é conhecida p pula
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MOTA, Mariana Flávia da. "Investigação da mielotoxicidade e do potencial indutor de morte celular de Synadenium umbellatum Pax. em células do tumor ascítico de Ehrlich." Universidade Federal de Goiás, 2010. http://repositorio.bc.ufg.br/tede/handle/tde/2134.

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Made available in DSpace on 2014-07-29T16:11:54Z (GMT). No. of bitstreams: 1 mariana mota.pdf: 5250493 bytes, checksum: f500835835d88733c77f12bd10fa8a80 (MD5) Previous issue date: 2010-03-03<br>In search of new antineoplasic agents natural products have played an important role, given that about 40% of available medicines in current treatments have been developed from natural sources, 25% approximately of plants. Synadenium umbellatum belongs to Euphorbiaceae family and is popularly known as "cola-nota", "avelós," "milagrosa", "cancerola", and the latex is empirically used in Brazil for the
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"Regulation of glucose transport system in Ehrlich ascites tumour cells." Chinese University of Hong Kong, 1987. http://library.cuhk.edu.hk/record=b5885819.

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Books on the topic "Ehrlich’s ascites tumour"

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Piayda, Ralf-Peter. Einfluss von Imipramin und Analoga auf Ionentransport und Volumenregulation bei Ehrlich-Maus-Ascites-Tumor-Zellen. 1988.

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Gukovskaya, A. Mechanisms of Receptor-Mediated Generation of Ionic Signals in Rat Thymocytes and Ehrlich Ascites Tumor Cells. Routledge, 1990.

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Lipson, Manuel Jacob. Response of Virus-Like Particles in Ehrlich Ascites Tumor Cells to Several Pharmacological Agents As Seen with the Electron Microscope. Creative Media Partners, LLC, 2021.

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Book chapters on the topic "Ehrlich’s ascites tumour"

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Lambert, Ian Henry. "Regulation of the Taurine Content in Ehrlich Ascites Tumour Cells." In Advances in Experimental Medicine and Biology. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4899-0117-0_34.

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Grune, Tilman, Werner Siems, Rolf Uhlig, Peter Langen, and Gerhard Gerber. "Changes of Purine Nucleotide Metabolism of Ehrlich Ascites Cells During Transition of Tumour Growth." In Advances in Experimental Medicine and Biology. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4899-2638-8_24.

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Kuznicki, Jacek, and Anna Filipek. "Calcyclin-Like Protein from Ehrlich Ascites Tumour Cells - Ca2+ -Binding Properties, Distribution and Target Protein." In Advances in Experimental Medicine and Biology. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4684-5754-4_24.

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Fujimura, S., A. Okamura, Y. Ohmura, et al. "Nicotinamide Methyltransferase Activity and Cell-Death in the Liver of the Mouse Bearing Ehrlich Ascites Tumor." In Advances in Experimental Medicine and Biology. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0381-7_78.

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Thiry, Marc, and Dominique Ploton. "Isolation of Nucleoli from Ehrlich Ascites Tumor Cells and Dynamics of Nascent RNA within Isolated Nucleoli." In The Nucleus. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-406-3_8.

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Akine, Yasuyuki, Nobuhiko Tokita, Koichi Tokuuye, et al. "Gadolinium Neutron Capture Therapy: Growth Suppression of Ehrlich Ascites and Subcutaneously-Implanted Tumor Cells in Mice." In Advances in Neutron Capture Therapy. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2978-1_48.

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Siems, W. G., T. Grune, H. Schmidt, et al. "Purine Nucleotides, Nucleosides and Nucleobases of Liver, Skeletal Muscle, Blood and Tumor Cells During the Growth of Ehrlich Ascites Tumor in Mice." In Advances in Experimental Medicine and Biology. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4899-2638-8_25.

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Siems, Werner G., Tilman Grune, Beatrix Beierl, Helmward Zollner, and Hermann Esterbauer. "The metabolism of 4-hydroxynonenal, a lipid peroxidation product, is dependent on tumor age in Ehrlich mouse ascites cells." In Free Radicals and Aging. Birkhäuser Basel, 1992. http://dx.doi.org/10.1007/978-3-0348-7460-1_13.

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Korohoda, W., and J. Kajstura. "Motile Activities in Polynuclear Products of Cell Fusion. I. Actin Rearrangements in Spreading on Glass Polycaryons Formed from Ehrlich Ascites Tumour Cells." In Protoplasma. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9008-1_12.

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Nakajima, Kenji. "Amelioration Effect of a Tertiary Sulfonium Compound, Dimethylsulfoniopropionate, in Green Sea Algae on Ehrlich Ascitic-tumor, Solid Tumor and Related Diseases." In Handbook of Anticancer Drugs from Marine Origin. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-07145-9_11.

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Conference papers on the topic "Ehrlich’s ascites tumour"

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Luksiene, Zivile, G. Kaspariunaite, E. Aleknavicius, and Konstantinas P. Valuckas. "Enhancement of photosensitization efficiency by various combinations with radiosensitization in an experimental Ehrlich ascites tumor." In BiOS Europe '96, edited by Stanley B. Brown, Benjamin Ehrenberg, and Johan Moan. SPIE, 1996. http://dx.doi.org/10.1117/12.260776.

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Othman, Azza I., Nariman K. Badr El-Din, Maggie E. Amer, and Mamdooh Ghoneum. "Abstract 7: Gross thymic extract inhibits tumor growth by modulating the immune response in mice bearing Ehrlich ascites carcinoma cells." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-7.

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Belyakova, T. A., V. E. Balakin, O. M. Rozanova, et al. "THE IMPACT OF TARGET VOLUMES OF EHRLICH ASCITES CARCINOMA IRRADIATED WITH A PENCIL SCANNING BEAM OF PROTONS AT A TOTAL DOSE OF 60 Gy ON THE TUMOR GROWTH AND REMOTE EFFECTS IN MICE." In RAD Conference. RAD Centre, 2020. http://dx.doi.org/10.21175/radproc.2020.05.

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