4 results on '"tumour to background ratio"'
Search Results
2. GPR87 is an overexpressed G-protein coupled receptor in squamous cell carcinoma of the lung.
- Author
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Gugger, Mathias, White, Richard, Song, Susan, Waser, Bea, Cescato, Renzo, Rivière, Pierre, and Reubi, Jean Claude
- Subjects
- *
LUNG cancer , *SQUAMOUS cell carcinoma , *CANCER treatment , *LUNG cancer diagnosis , *MOLECULAR structure - Abstract
Lung cancer is the leading cause of cancer death worldwide. The overall 5-year survival after therapy is about 16% and there is a clear need for better treatment options, such as therapies targeting specific molecular structures. G-protein coupled receptors (GPCRs), as the largest family of cell surface receptors, represent an important group of potential targets for diagnostics and therapy. We therefore used laser capture microdissection and GPCR-focused Affymetrix microarrays to examine the expression of 929 GPCR transcripts in tissue samples of 10 patients with squamous cell carcinoma and 7 with adenocarcinoma in order to identify novel targets in non-small cell lung carcinoma (NSCLC). The relative gene expression levels were calculated in tumour samples compared to samples of the neighbouring alveolar tissue in every patient. Based on this unique study design, we identified 5 significantly overexpressed GPCRs in squamous cell carcinoma, in the following decreasing order of expression: GPR87 > CMKOR1 > FZD10 > LGR4 > P2RY11. All are non-olfactory and GRAFS (glutamate, rhodopsin, adhesion, frizzled/taste2, secretin family) classified. GPR87, LGR4 and CMKOR1 are orphan receptors. GPR87 stands out as a candidate for further target validation due to its marked overexpression and correlation on a mutation-based level to squamous cell carcinoma. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
3. GPR87 Is an Overexpressed G-Protein Coupled Receptor in Squamous Cell Carcinoma of the Lung
- Author
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Susan Song, Pierre Rivière, Mathias Gugger, Jean Claude Reubi, Renzo Cescato, Richard White, and B. Waser
- Subjects
squamous cell carcinoma ,Quality Control ,Lung Neoplasms ,molecular targets ,laser capture microdissection ,Blotting, Western ,Clinical Biochemistry ,Gene Expression ,Adenocarcinoma ,Biology ,tumour to background ratio ,Cell surface receptor ,Genetics ,medicine ,Carcinoma ,Humans ,RNA, Messenger ,Receptors, Lysophosphatidic Acid ,Lung cancer ,Receptor ,Molecular Biology ,Oligonucleotide Array Sequence Analysis ,Laser capture microdissection ,G protein-coupled receptor ,cDNA microarray ,lcsh:R5-920 ,Squamous-cell carcinoma of the lung ,GPR87 ,Reverse Transcriptase Polymerase Chain Reaction ,Lasers ,Biochemistry (medical) ,General Medicine ,medicine.disease ,Immunohistochemistry ,Molecular biology ,Pulmonary Alveoli ,G-protein coupled receptor ,Carcinoma, Squamous Cell ,Cancer research ,Other ,lcsh:Medicine (General) ,Microdissection - Abstract
Lung cancer is the leading cause of cancer death worldwide. The overall 5-year survival after therapy is about 16% and there is a clear need for better treatment options, such as therapies targeting specific molecular structures. G-protein coupled receptors (GPCRs), as the largest family of cell surface receptors, represent an important group of potential targets for diagnostics and therapy. We therefore used laser capture microdissection and GPCR-focused Affymetrix microarrays to examine the expression of 929 GPCR transcripts in tissue samples of 10 patients with squamous cell carcinoma and 7 with adenocarcinoma in order to identify novel targets in non-small cell lung carcinoma (NSCLC). The relative gene expression levels were calculated in tumour samples compared to samples of the neighbouring alveolar tissue in every patient. Based on this unique study design, we identified 5 significantly overexpressed GPCRs in squamous cell carcinoma, in the following decreasing order of expression: GPR87 > CMKOR1 > FZD10 > LGR4 > P2RY11. All are non-olfactory and GRAFS (glutamate, rhodopsin, adhesion, frizzled/taste2, secretin family) classified. GPR87, LGR4 and CMKOR1 are orphan receptors. GPR87 stands out as a candidate for further target validation due to its marked overexpression and correlation on a mutation-based level to squamous cell carcinoma.
- Published
- 2008
4. Relationship between primary tumour 18 F-FDG uptake and immunohistochemical and clinical prognostic parameters in breast carcinoma.
- Author
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Gedik GK, Yilmaz F, and Sari O
- Subjects
- Adult, Aged, Aged, 80 and over, Female, Humans, Immunohistochemistry, Middle Aged, Prognosis, Retrospective Studies, Breast Neoplasms diagnostic imaging, Breast Neoplasms metabolism, Fluorodeoxyglucose F18 pharmacokinetics, Positron Emission Tomography Computed Tomography, Radiopharmaceuticals pharmacokinetics
- Abstract
Objective: The objective of this study was to investigate the relationship between level of
18 F-fluorodeoxyglucose (18 F-FDG) accumulation in primary breast tumour assessed by positron emission tomography/computed tomography (PET/CT) and histopathological and clinical prognostic factors., Material and Methods: A retrospective analysis was performed using the medical records of 58 female patients (age range: 31-86 years, mean age: 56) with biopsy of proven breast carcinoma, and who had undergone18 F-FDG PET/CT examination before chemotherapy/surgery. The18 F-FDG uptake of breast tumours was calculated as tumour to background ratio (TBR), which was compared with histopathological and clinical prognostic parameters., Results: The histology of the breast tumour in the 58 patients was ductal type in 52 (90%), lobular in 4 (7%), and mucinous in 2 (3%). Tumour size was ≤ 2cm in 31 (53%) patients, and>2cm in 27 (47%). The levels of TBRs were not significantly different between the patients groups with tumours of 2cm or less and greater than 2cm (P=0.131). No significant difference between levels of TBR was observed neither with regards to axillary lymph node involvement (P=0.065) nor in terms of distant metastases (p=0.123). No statistically significant difference was found in levels of TBRs between patients with c-erbB-2 receptor positive and negative ones (P=0.107). Progesterone receptor (PR) expression was observed in 33 patients (57%), and 25 patients (43%) were PR negative. As regards progesterone receptor status, a statistically significant difference was observed in mean TBR levels between patients with and without progesterone receptor expression (P=0.020). Oestrogen receptor expression was positive in 41 (71%) patients, and negative in 17 (29%) patients. The difference in the levels of TBRs between patients with and without oestrogen receptor expression was at the level of significancy (P=0.050)., Conclusions: It is concluded that18 F-FDG uptake correlates with progesterone negativity of the tumour. However, a significant association with clinical prognostic parameters and level of18 F-FDG uptake levels could not be demonstrated., (Copyright © 2016 Elsevier España, S.L.U. y SEMNIM. All rights reserved.)- Published
- 2017
- Full Text
- View/download PDF
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