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1.
BMC Cancer ; 16: 618, 2016 08 09.
Article in English | MEDLINE | ID: mdl-27507139

ABSTRACT

BACKGROUND: The minor allele of two caspase 8 polymorphisms, namely CASP8 -652 6N InsDel (rs3834129) and CASP8 Asp302His (rs1045485), were repeatedly associated with reduced breast cancer susceptibility. Contrarily, the presence of the -652 6N Del or the CASP8 302His variant was reported to be an unfavorable prognostic factor in colorectal cancer or neuroblastoma. However, prognostic relevance of these genetic variants for breast cancer is completely unknown and is therefore adressed by the current study. METHODS: Genotyping was performed by pyrosequencing. Caspase 8 mRNA expression was quantified by comparative RT-qPCR. RESULTS: We observed an allele-dose dependent association between CASP8 -652 6N InsDel and caspase 8 mRNA expression in breast cancer tissue, with homozygous deletion carriers showing lowest relative caspase 8 expression (p = 0.0131). Intriguingly, the presence of the -652 6N Del or the 302His variant was shown to be a negative prognostic factor for breast cancer in terms of an allele-dose dependent influence on overall survival (OS, p = 0.0018, p = 0.0150, respectively). Moreover, both polymorphisms were independent predictors of OS after adjusting for co-variats (p = 0.007, p = 0.037, respectively). Prognostic relevance of both polymorphisms were confirmed to be independent from each other and combined analysis of diplotypes revealed an additive influence upon OS (p = 0.0002). CONCLUSION: This is the first report, showing negative and independent prognostic impact of the CASP8 -652 6N Del and the 302His variant for breast cancer. Our data provide rationale to further validate clinical utility of these polymorphisms for breast cancer and to extend this investigation to a broad scope of other malignancies.


Subject(s)
Breast Neoplasms/genetics , Caspase 8/genetics , Genetic Predisposition to Disease/genetics , Adult , Aged , Breast Neoplasms/mortality , Case-Control Studies , Female , Genotype , Humans , Kaplan-Meier Estimate , Middle Aged , Polymorphism, Single Nucleotide , Prognosis , Proportional Hazards Models , Real-Time Polymerase Chain Reaction
2.
Article in German | MEDLINE | ID: mdl-19204399

ABSTRACT

OBJECTIVE: About 3-4% of all pregnant women will have a fetus presenting by the breech at term. External cephalic version offers the opportunity to reduce the rate of caesarean sections caused by breech presentation. We analysed retrospectively 51 cases of external cephalic version at our clinic. METHODS: External cephalic version was performed 51 times between 37 and 41 weeks of pregnancy. RESULTS: External cephalic version was successful in 32/51 cases (62,7%) with a consecutive rate of vaginal delivery of 71,9%. The best results were seen at 37 weeks of pregnancy with 81,25% of successful versions followed by 76,9% of vaginal deliveries. Complications were rare. There was just 1 case of emergency caesarean section due to persisting fetal bradycardia. CONCLUSION: External cephalic version is an effective and safe treatment to enable vaginal delivery of cephalic presentation. For this operation, 37 weeks of pregnancy can be considered the best time.


Subject(s)
Breech Presentation/nursing , Breech Presentation/rehabilitation , Version, Fetal/instrumentation , Version, Fetal/methods , Adult , Female , Humans , Pregnancy , Treatment Outcome , Version, Fetal/adverse effects
3.
Pathologe ; 29 Suppl 2: 357-62, 2008 Nov.
Article in German | MEDLINE | ID: mdl-18841368

ABSTRACT

Aquaporin1 (AQP1) is a water channel protein which facilitates water flux across cell membranes. AQP1 is found in epithelial and endothelial cells in various tissues. There is increasing evidence that AQP1 is expressed in malignant tumours and that it may play a role in tumour angiogenesis, cell migration and metastasis. We studied the immunohistochemical expression of AQP1 in a cohort of 203 invasive breast carcinomas with long-term follow up. AQP1 expression was detected in 11 cases (5.4%), and showed a significant correlation with high tumour grade, medullary-like histology, "triple-negativity", as well a cytokeratin 14 and actin expression. In univariate analysis, AQP1 was associated with a significantly poorer prognosis. Multivariate analysis showed that AQP1 expression has an independent predictive value for outcome if stratified by age, tumour size, lymph node status, histological grade and ER status. AQP1 expression in invasive breast carcinomas is associated with a basal-like phenotype and poor prognosis.


Subject(s)
Aquaporin 1/genetics , Biomarkers, Tumor/genetics , Breast Neoplasms/genetics , Carcinoma, Ductal/genetics , Carcinoma, Lobular/genetics , Neoplasms, Hormone-Dependent/genetics , Receptors, Estrogen/genetics , Receptors, Progesterone/genetics , Actins/genetics , Breast/pathology , Breast Neoplasms/mortality , Breast Neoplasms/pathology , Carcinoma, Ductal/mortality , Carcinoma, Ductal/pathology , Carcinoma, Lobular/mortality , Carcinoma, Lobular/pathology , Disease-Free Survival , Female , Follow-Up Studies , Humans , Kaplan-Meier Estimate , Keratin-14/genetics , Lymphatic Metastasis/pathology , Multivariate Analysis , Neoplasm Invasiveness , Neoplasms, Hormone-Dependent/pathology , Phenotype , Prognosis
4.
Zentralbl Gynakol ; 128(3): 149-52, 2006 Jun.
Article in German | MEDLINE | ID: mdl-16758382

ABSTRACT

INTRODUCTION: Antibiotic prophylaxis is a standard procedure in obstetric surgery and has been discussed in various investigations. Use of treatment is judged by high efficacy and good tolerance. METHOD: In 300 patients undergoing cesarean sections we compared results of application of Piperacillin 4 g and Piperacillin/Tazobactam 4.5 g after cut of umbilical cord. Tazobactam/Piperacillin is a combination of a broad-spectrum penicillin and a beta-lactamase inhibitor with increased toxicity against staph. aureus, enterobacter, and other germs responsible for local and systemic infections in obstetric surgery. RESULTS: We did not observe any severe adverse effects. Rate of severe wound infections was 1.3 % (Tazobactam/Piperacillin) and 2 % (Piperacillin alone). The difference showed no statistic significance (p > 0.01). During postoperative course we found a higher increase of CRP (p < 0.01) in the Piperacillin group. CRP proved to be a useful objective parameter to distinguish between patients with or without postoperative infections. No differences were found in the number of leucocytes, time in hospital and other parameters.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Antibiotic Prophylaxis , Cesarean Section/methods , Penicillanic Acid/analogs & derivatives , Piperacillin/therapeutic use , Drug Therapy, Combination , Enzyme Inhibitors/therapeutic use , Female , Humans , Microbial Sensitivity Tests , Penicillanic Acid/therapeutic use , Pregnancy , Tazobactam
5.
J Clin Pathol ; 59(7): 685-91, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16497869

ABSTRACT

BACKGROUND AND AIM: The production of prostaglandins is regulated by cyclo-oxygenases (COXs), which also have a role in tumour development and progression in various malignancies, including breast cancer. The mechanisms by which COX-2 contributes to unfavourable prognosis are still poorly understood. The association between expression of COX-2 and possible linked signalling pathways-namely, Akt, extracellular regulated kinases (ERK1/2), the stress-activated kinase p38 or Her-2/neu-is assessed in a series of 113 node-negative breast cancers. RESULTS: COX-2 was identified as an independent prognostic factor (p = 0.034) in node-negative breast cancer by survival analysis. The lack of a relationship between COX-2 expression and activated Akt, Erk1/2, p38 and Her-2/neu was indicated by statistical analysis. CONCLUSIONS: The prognostic effect of COX-2 expression on lymph node-negative breast cancer is confirmed-COX-2 is probably not regulated by HER-2, Akt, Erk1/2 or p38. Further studies are necessary for the elucidation of the signalling pathways responsible for the modification of COX-2 expression and the increased aggressiveness of breast cancers overexpressing COX-2.


Subject(s)
Biomarkers, Tumor/metabolism , Breast Neoplasms/enzymology , Cyclooxygenase 2/metabolism , Neoplasm Proteins/metabolism , Aged , Breast Neoplasms/metabolism , Breast Neoplasms/pathology , Female , Follow-Up Studies , Humans , In Situ Hybridization, Fluorescence , Middle Aged , Prognosis , Proto-Oncogene Proteins c-akt/metabolism , Receptor, ErbB-2/metabolism , Signal Transduction , Survival Analysis , p38 Mitogen-Activated Protein Kinases/metabolism
6.
Virchows Arch ; 448(1): 16-23, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16208531

ABSTRACT

The Akt signalling pathway plays a central role in tumourigenesis. Activation of Akt is related to a more aggressive phenotype in various human cancers, including breast cancer. Its activation contributes to cancer progression via pleiotropic effects, including suppression of apoptosis and modulation of cell cycle regulation. Murine double minute 2 (MDM2) is an oncoprotein that inhibits the function of p53 tumour suppressor protein. Cell culture studies show that Akt-related phosphorylation of MDM2 at serine 166 allows MDM2 to gain nuclear entry and fulfil its p53 regulating function. This study was designed to analyse the relationship of phospho-MDM2 (pMDM2) expression with Akt activation to determine a possible prognostic relevance of pMDM2 in node-negative breast cancer with respect to Akt activation and p53 status. pMDM2, phospho-Akt (pAkt) and p53 protein expression status were analysed immunohistochemically in 121 paraffin-embedded breast cancer cases. Expression of pMDM2 correlated with Akt activation (P<0.001). Univariate analysis identified pMDM2 as a prognostic factor (P=0.0458) in node-negative breast cancers. The unfavourable prognostic significance was even more pronounced in tumours with a pMDM2(+)/pAkt(+) immunophenotype (P=0.0205). Stratification into a p53-negative subgroup further strengthened the adverse prognostic influence. These data confirm that MDM2 phosphorylation at serine 166 is mediated by Akt kinase. Besides the prognostic impact of pMDM2, our findings suggest that Akt-mediated modulation of the MDM2/p53 complex contributes to increased tumour aggressiveness especially in p53-negative breast cancers. However, due to the relatively small number of patients in this cohort, the results obtained need to be confirmed by larger cohorts.


Subject(s)
Breast Neoplasms/metabolism , Proto-Oncogene Proteins c-akt/metabolism , Proto-Oncogene Proteins c-mdm2/metabolism , Receptor Cross-Talk/physiology , Tumor Suppressor Protein p53/metabolism , Biomarkers, Tumor/metabolism , Breast Neoplasms/pathology , Female , Humans , Immunohistochemistry , Lymphatic Metastasis/pathology , Middle Aged , Phosphorylation , Prognosis
7.
8.
Eur J Gynaecol Oncol ; 19(4): 377-83, 1998.
Article in English | MEDLINE | ID: mdl-9744730

ABSTRACT

OBJECTIVE: Cellular adhesion molecules ICAM-1 and VCAM-1 have been implicated in tumor progression and metastasis. As the sequential interaction of neoplastic cells with the endothelium of tumor neovascularisation is believed to be essential for tumor metastasizing processes, we analysed the concentration of ICAM-1 and VCAM-1 in the cytosol of patients with human breast cancers and their corresponding sera. We compared the obtained values with established prognostic parameters for breast cancer. Benign breast tissues were also analyzed. PATIENTS AND METHODS: Levels of ICAM-1 and VCAM-1 of 62 patients with invasive breast cancer and 17 patients with benign breast tissue were measured using commercially available sandwich enzyme-linked immunoassays with monoclonal antibodies. To establish a reference and control group, levels of ICAM-1 and VCAM-1 were measured in the sera of 66 women without breast tumors. RESULTS: The mean cytosol concentration of ICAM-1 and VCAM-1 was significantly higher in the breast cancer specimens than in the tissue of patients with benign breast diseases. This could be found not only in the tumor cytosol but also in the corresponding sera of the patients. No correlations between the ICAM-1 and VCAM-1 expressions and established prognostic parameters could be observed. CONCLUSIONS: Our findings suggest that malignant breast cancer cells could induce neovascularisation with subsequent high expressions of ICAM-1 and VCAM-1. These upregulations of adhesion molecules might contribute to changes in invasive phenotypes by promoting endothelial cell adhesion and angiogenesis, as well as being responsible for the recognition of tumor cells by the human immune system. Prognostic relevance for the development of breast cancer could not be established.


Subject(s)
Breast Neoplasms/blood , Breast Neoplasms/metabolism , Breast/metabolism , Intercellular Adhesion Molecule-1/metabolism , Vascular Cell Adhesion Molecule-1/metabolism , Adult , Breast Neoplasms/diagnosis , Cytosol/metabolism , Enzyme-Linked Immunosorbent Assay , Female , Humans , Intercellular Adhesion Molecule-1/blood , Middle Aged , Prognosis , Vascular Cell Adhesion Molecule-1/blood
9.
Article in German | MEDLINE | ID: mdl-9658712

ABSTRACT

The rare case of a decidualized endometriosis of the appendix vermiformis is reported in a woman who developed HELLP syndrome during the 32nd week of a twin pregnancy. Cesarean section and simultaneous appendectomy were performed. An inspection of the appendix should always be carried out if an endometriosis-associated anamnesis is known. No pathophysiological correlations between the HELLP syndrome and the endometriosis of the appendix vermiformis could be found.


Subject(s)
Appendix , Cesarean Section , Endometriosis/complications , HELLP Syndrome/complications , Pregnancy Complications/surgery , Adult , Appendectomy , Appendix/pathology , Endometriosis/pathology , Endometriosis/surgery , Female , HELLP Syndrome/pathology , HELLP Syndrome/surgery , Humans , Pregnancy , Pregnancy Complications/pathology , Pregnancy, Multiple , Twins
10.
Eur J Gynaecol Oncol ; 18(5): 353-60, 1997.
Article in English | MEDLINE | ID: mdl-9378152

ABSTRACT

UNLABELLED: BACKGROUND AND QUESTION: A retrospective study was performed. To check the hypothesis whether there is an inverse connection between age and prognosis. PATIENTS AND METHODS: We investigated a total group of 1000 cases with breast cancer primarily and consecutively treated between 1968 and 1986. After grouping the patients by tumor stage and median age various life table analyses were performed to calculate and compare the overall survival. Entry date was the date at diagnosis of a first breast cancer or date at first diagnosis of distant metastasis. RESULTS: Young patients with a tumor size T1 and T2 had a significantly better prognosis than older patients with the same tumor stage. Influence of age became significantly weaker in patients with a T3 and T4 tumor. At least in the patients with a primarily M1 stage hardy any more dependence of age could be demonstrated. Similar results were obtained for the 198 patients which presented a distant recurrence. CONCLUSION: Better general life expectancy of young patients is the cause of substantially better overall survival in curable stages. Advanced breast cancer is a strongly life-threatening factor. The fatal influence of large tumor mass is independent of age.


Subject(s)
Aging/physiology , Breast Neoplasms/pathology , Aged , Breast Neoplasms/therapy , Female , Humans , Middle Aged , Neoplasm Staging , Prognosis , Retrospective Studies , Survival Analysis
11.
Biotechnol Bioeng ; 56(1): 56-61, 1997 Oct 05.
Article in English | MEDLINE | ID: mdl-18636609

ABSTRACT

We mapped the distribution of dissolved oxygen and mammalian cells in a hollow-fiber bioreactor (HFBR) using (19)F NMR T(1) relaxation time imaging measurements on an infused perfluorocarbon probe molecule and diffusion-weighted (1)H NMR imaging of water. This study shows how cell density influences dissolved oxygen concentration in the reactor and demonstrates that NMR can play an important role in defining the biochemical engineering parameters required for optimization of HFBR design and operation.

12.
Eur J Gynaecol Oncol ; 17(3): 192-9, 1996.
Article in English | MEDLINE | ID: mdl-8780917

ABSTRACT

INTRODUCTION: Mutations of the tumor suppressor gene p53 are common in multiple cancer forms, including breast cancer. Data are available that suggest, that the loss of the wild type form of p53 and the appearance of the mutant forms of p53 are correlated with a poorer overall survival rate in patients with breast cancer. The accumulation of the mutant forms of p53 in the cytoplasmatic rooms of the tumor cells leads to the production of human auto-antibodies against these mutant p53 proteins. Therefore, the aim of this study was to analyse and quantify the levels of serum auto-antibodies against p53 protein in patients with an intact immunological system having an active and new recurrence of breast cancer and to compare the obtained results with the recurrence free interval and with established prognostic parameters at the time of first diagnosis, to see if patients with a positive p53 auto-antibody status had a poorer prognosis than those who were p53 auto-antibody positive. MATERIALS AND METHODS: The ser of 61 patients with breast cancer, who experienced a new, clinical and biophysically identified local or distant recurrence and that showed an intact immunological system were analysed with an ELISA assay of Dianova to determine the concentration of auto-antibodies against mutant p53. RESULTS: 14.5% of the patients showed a positive p53 auto-antibody serum status. The recurrence free interval between the p53 auto-antibody positive and negative patients was almost the same: 4.12 years for the p53 auto-antibody positive patients versus 3.72 years for the p53 auto-antibody negative patients (independent t-test value = 0.224 and p value = 0.824; statistically not a significant difference). When comparing the p53 auto-antibody status with established prognostic parameters we could only find a statistically significant correlation with tumor size. No correlations were obtained when comparing the p53 auto-antibody status with the N- and M status, the ER- and PR status, the menopausal status and the cathepsin-D status. DISCUSSION: We were able to demonstrate that the expression of serum auto-antibodies against mutant p53 can not be used as a prognostic parameter in patients with breast cancer as the recurrence free interval between the p53 auto-antibody positive and negative patients did not differ. The determination of the auto-antibodies against p53, though easy to perform, is therefore not a test that helps clinicians in their treatment options, but it remains a useful test for the description of the biological mechanisms of breast cancer.


Subject(s)
Autoantibodies/blood , Breast Neoplasms/immunology , Neoplasm Recurrence, Local/immunology , Tumor Suppressor Protein p53/immunology , Breast Neoplasms/therapy , Enzyme-Linked Immunosorbent Assay , Female , Humans , Mutation , Prognosis
13.
Arch Gynecol Obstet ; 258(3): 125-35, 1996.
Article in English | MEDLINE | ID: mdl-8781700

ABSTRACT

Eighty one invasive breast cancers were analysed immunohistochemically to detect if they expressed the adhesion molecules CD44 v6 and v4/5, and the results were evaluated using the semiquantitative IR-score. The results were further divided into four groups: negative, weak positive, moderate positive and strong positive. Fifteen benign breast tumors were also analysed. Sixty eight breast cancers were CD44v6 and v4/5 positive. T3 and T4 cancers showed statistically significant higher positive CD44 rates than T1 and T2 cancers (P < 0.05). We also found a statistically significant correlation between the estrogen receptor and the CD44 status and between the CD44 status and the cathepsin-D status, whereas no correlation between CD44 and the lymph node status, the M status, the grading of the tumors, the progesterone receptor and the menopausal status could be found. Eleven benign tumors were CD44v6 and v4/5 positive. We could not establish any correlation between the expression of CD44 and the metastasizing capacity of breast cancer.


Subject(s)
Breast Neoplasms/genetics , Carcinoma, Ductal, Breast/genetics , Carcinoma, Lobular/genetics , Hyaluronan Receptors/genetics , Breast/pathology , Breast Neoplasms/pathology , Carcinoma, Ductal, Breast/pathology , Carcinoma, Lobular/pathology , Cathepsin D/blood , Female , Humans , Hyaluronan Receptors/classification , Lymph Nodes/pathology , Lymphatic Metastasis , Neoplasm Invasiveness , Prognosis
14.
Eur J Obstet Gynecol Reprod Biol ; 63(1): 69-73, 1995 Nov.
Article in English | MEDLINE | ID: mdl-8674569

ABSTRACT

OBJECTIVES: The steroid receptor concentration and the histological morphology of uterine leiomyomata in premenopausal patients undergoing myomectomy therapy with and without a preoperative GnRH analogue, was analysed to evaluate whether the GnRH analogue therapy leads to important hormonal receptor changes, histomorphological changes and a significant shrinkage of the leiomyomata. STUDY DESIGN: Sixty-one GnRH analogue pretreated leiomyomata and 28 untreated leiomyomata were analysed. To determine the estrogen and progesterone receptor concentrations, immunohistochemical techniques were used and quantified with the immuno-reactive score (IRS-score). The leiomyomata were divided into cellular rich, normal, hyaline or cystic degenerated and necrotic according to their histology. RESULTS: The GnRH analogue pretreated leiomyomata group showed higher levels of estrogen and progesterone receptors than the untreated group (37.7% of the GnRH analogue group had a high positive and 29.5% a moderate positive estrogen receptor status whereas high levels of estrogen receptor could be found in only 14.3% of the untreated group). The leiomyomata of both groups with the exception of the necrotic ones, were estrogen and progesterone receptor positive. CONCLUSIONS: Our study suggests that pretreatment of uterine leiomyomata leads to a significant increase in the hormonal receptor concentration of these benign tumors. If pretreated leiomyomata are not removed surgically immediately after the therapy, a rapid regrowth can occur and again cause clinical symptoms.


Subject(s)
Antineoplastic Agents, Hormonal/therapeutic use , Leiomyoma/metabolism , Leuprolide/therapeutic use , Receptors, Estrogen/metabolism , Receptors, Progesterone/metabolism , Uterine Neoplasms/metabolism , Female , Humans , Immunohistochemistry , Leiomyoma/drug therapy , Leiomyoma/surgery , Premenopause , Uterine Neoplasms/drug therapy , Uterine Neoplasms/surgery
15.
Aktuelle Radiol ; 5(4): 263-7, 1995 Jul.
Article in German | MEDLINE | ID: mdl-7548257

ABSTRACT

AIM: To compare in mammography the image quality of digital luminescence radiography (DLR) to that of usual film screen mammography and xeromammography. MATERIALS AND METHODS: Three single emulsion film-screen combinations, one double coated high resolution film and xeroradiography, were tested for this purpose. In our phantom study the detectability of microcalcifications, fibrils and low contrast details were first of all studied separately. Image processing techniques were, for example, contrast variation by grey scale level windowing, "unsharp mask" filtering and regulatable edge enhancement. Phantom images were made and then the image quality was evaluated by observer performance study using a receiver operating characteristic (ROC analysis). RESULTS: Best results in respect of detection of microcalcifications and fibrils were found in xeroradiography, luminescent image plate and double-coated film-screen combination. These systems showed more favourable ROC curves than the single emulsion film-screen combinations. CONCLUSIONS: Our results indicate that image quality of digital images in the field of image processing is equal to that of conventional mammographic techniques and partially superior to detection of low contrast details.


Subject(s)
Breast Neoplasms/diagnostic imaging , Mammography/instrumentation , Radiographic Image Enhancement/instrumentation , Radiographic Magnification/instrumentation , X-Ray Intensifying Screens , Xeromammography/instrumentation , Calcinosis/diagnostic imaging , Female , Humans , Mammography/statistics & numerical data , Models, Anatomic , ROC Curve , Xeromammography/statistics & numerical data
16.
Eur J Gynaecol Oncol ; 16(2): 130-7, 1995.
Article in English | MEDLINE | ID: mdl-7641740

ABSTRACT

The concentration of c-erbB-2 oncoprotein (HER-2/neu) was examined in the membrane fraction of 196 breast cancer and 39 benign breast specimens using a recently introduced ELISA-assay. The results were compared with established clinical and laboratory prognostic factors, 19% of all breast cancer specimens showed a c-erbB-2 protein level above 10 HNU/micrograms extract protein and were so classified as positive. Considering only the samples of primary tumors the rate was 21%. Surprisingly the rate was only 13.5% in the tissue samples of recurrent disease. Significant correlations were found between high c-erbB-2 protein levels and the tumor diameter, the axillary lymph node status and the progesterone receptor status. In contrast no correlation was found with estrogen receptor or menopausal status. All specimens of benign tumors showed levels < 10 HNU/micrograms extract protein and were classified as negative. The measurement of the c-erbB-2 protein using this ELISA assay was simple to perform and revealed reliable results. Nevertheless the prognostic power of the c-erbB-2 protein seems to be of minor relevance in comparison with established clinical and laboratory parameters, as the positive rates are too small in regard to the much higher recurrence rates of breast cancer. Probably the serum levels of this oncoprotein will be of greater clinical interest in the course of breast cancer.


Subject(s)
Breast Diseases/metabolism , Breast Neoplasms/chemistry , Receptor, ErbB-2/analysis , Breast Neoplasms/ultrastructure , Enzyme-Linked Immunosorbent Assay , Female , Humans , Immunohistochemistry , Menopause , Neoplasm Staging , Receptors, Estrogen/analysis , Receptors, Progesterone/analysis , Tissue Fixation
17.
Biotechnology (N Y) ; 12(1): 75-8, 1994 Jan.
Article in English | MEDLINE | ID: mdl-7764329

ABSTRACT

We have used diffusion-weighted 1H NMR micro-imaging and localized spectroscopy techniques to monitor the growth and distribution of mammalian cells in a hollow-fiber bioreactor. Non-invasive NMR measurements of this type should also allow investigation of metabolic heterogeneity and assist in future designs of hollow-fiber systems.


Subject(s)
Cells/cytology , Magnetic Resonance Spectroscopy , Cell Division , Cytological Techniques , Diffusion , Kinetics , Spectrum Analysis , Water
18.
Magn Reson Med ; 29(4): 546-50, 1993 Apr.
Article in English | MEDLINE | ID: mdl-8464371

ABSTRACT

The appearance of high resolution neutral lipid signals in the 1H NMR spectra of myeloma cells grown in the presence of oleate was shown to correlate with the appearance of cytoplasmic lipid droplets observable by electron microscopy. The spin-spin relaxation times of these lipid signals were similar to those measured previously for lipid resonances in other cell types. These data suggest that cytoplasmic lipid droplets could make a significant contribution to the neutral lipid signals observed in the 1H NMR spectra of some cells.


Subject(s)
Lipid Metabolism , Magnetic Resonance Spectroscopy , Multiple Myeloma/metabolism , Animals , Cytoplasm/metabolism , In Vitro Techniques , Mice , Microscopy, Electron , Multiple Myeloma/pathology , Oleic Acid , Oleic Acids , Tumor Cells, Cultured
19.
Plant Physiol ; 100(3): 1584-6, 1992 Nov.
Article in English | MEDLINE | ID: mdl-16653163

ABSTRACT

Nuclear magnetic resonance offers the possibility of noninvasive in situ observation of (15)N pulse labeling in the presence of light. In vivo, exclusively the delta-nitrogen of Gln is labeled in the cyanobacterium Microcystis firma when glutamate synthase is inhibited by azaserine. In contrast, the green alga Chlorella fusca is additionally capable of incorporating nitrogen into Glu, thus providing evidence for an anabolic function of glutamate dehydrogenase in this organism.

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