نتایج جستجو برای: tumor burden

تعداد نتایج: 524097  

Journal: :Cancer research 1977
J Eipe V Yakulis N Costea

These studies examined the fate of Factor XIII (fibrin-stabilizing factor) in mice with plasmacytoma (MOPC-300, MOPC-384, MOPC-467, and J-558). Plasma Factor XIII levels in these mice decreased progressively with tumor expansion. No plasma inhibitors of Factor XIII activity could be detected. Factor XIII was found on plasmacytoma cell membranes and in the cytoplasm of the malignant cells by imm...

2017
Xin Yi Jianhui Ma Yanfang Guan Rongrong Chen Ling Yang Xuefeng Xia

For many decades it has been known that tumor DNA is shed into the blood. As a consequence of technological limitations, researchers were unable to comprehensively characterize circulating DNA. The advent of ultrasensitive and highly specific molecular assays has provided a comprehensive profile of the molecular characteristics and dynamics of circulating DNA in healthy subjects and cancer pati...

Journal: :Cancer research 2005
Andrew H Gordon Regis J O'Keefe Edward M Schwarz Randy N Rosier J Edward Puzas

A central mediator of a wide host of target genes, the nuclear factor-kappaB (NF-kappaB) family of transcription factors, has emerged as a molecular target in cancer and diseases associated with bone destruction. To evaluate how NF-kappaB signaling in tumor cells regulates processes associated with osteolytic bone tumor burden, we stably infected the bone-seeking MDA-MB-231 breast cancer cell l...

2016
Nikita Consul Xiaotao Guo Courtney Coker Sara Lopez-Pintado Hanina Hibshoosh Binsheng Zhao Kevin Kalinsky Swarnali Acharyya

Cachexia, a wasting syndrome associated with advanced cancer and metastasis, is rarely documented in breast cancer patients. However, the incidence of cachexia in breast cancer is now thought to be largely underestimated. In our case report of a breast cancer patient with bone metastasis monitored during the course of her treatment, we document the development of cachexia by image analysis in r...

2000
James W. Wilson Christopher S. Potten

This study set out to examine the effect of exogenous prostaglandin (PG) administration on tumor development in Min/1 mice. Mice were treated with the stable prostaglandin E2 analogue 16,16-dimethyl-PGE2 from 6–18 weeks of age. Mice were sacrificed, and tumor burden was assessed using morphometric techniques. Parameters measured were median tumor size, mean tumor size, the proportion of the are...

Journal: :Cancer research 2000
J W Wilson C S Potten

This study set out to examine the effect of exogenous prostaglandin (PG) administration on tumor development in Min/+ mice. Mice were treated with the stable prostaglandin E2 analogue 16,16-dimethyl-PGE2 from 6-18 weeks of age. Mice were sacrificed, and tumor burden was assessed using morphometric techniques. Parameters measured were median tumor size, mean tumor size, the proportion of the are...

Journal: :Annals of Cancer Research and Therapy 2021

Cancer is the leading cause of death worldwide. Despite significant advances in cancer treatment, morbidity and mortality rates remain high. Tumor heterogeneity, particularly intertumoral a major therapy failure, underpinning tumor treatment problems variety available therapeutic strategies, including molecularly targeted therapies. Recent massively parallel sequencing digital genomic technique...

2015
Aaron C. Ericsson Sadia Akter Marina M. Hanson Susheel B. Busi Taybor W. Parker Rebecca J. Schehr Miriam A. Hankins Carin E. Ahner Justin W. Davis Craig L. Franklin James M. Amos-Landgraf Elizabeth C. Bryda

Recent studies investigating the human microbiome have identified particular bacterial species that correlate with the presence of colorectal cancer. To evaluate the role of qualitatively different but naturally occurring gut microbiota and the relationship with colorectal cancer development, genetically identical embryos from the Polyposis in Rat Colon (Pirc) rat model of colorectal cancer wer...

Journal: :Cancer research 1987
F A Salinas K H Wee R L Ceriani

Use of monoclonal antibodies (Mc 3 and Mc 8) prepared against human mammary-epithelial antigens of human mild fat globule membranes has enabled characterization of breast carcinoma (BC) associated antigens (BCAA), antibodies, and circulating immune complexes (CIC). For this study, BC patients were grouped on the basis of measurable tumor burden: Group I patients with no evidence of disease at s...

2006
Fernando A. Salinas Kian H. Wee Roberto L. Ceriani

Use of monoclonal antibodies (Me 3 and Me 8) prepared against human mammary-epithelial antigens of human milk fat globule mem branes has enabled characterization of breast carcinoma (BC) associated antigens (BCAA), antibodies, and circulating immune complexes (CIC). For this study, BC patients were grouped on the basis of measurable tumor burden: Group I patients with no evidence of disease at ...

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