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L Suter

Publications and source records attributed to L Suter.

66 records · Page 4Linked to original sources

Membrane associated antigens of human malignant melanoma. II. Leucocyte migration studies with formalin fixed human melanoma cells.

The leucocyte migration test from caillary tubes was examined for its usefulness as an assay for cell-mediated immunity in melanoma patients. Formalin fixed melanoma cells either obtained from established cell lines or freshly excised tumors were used as antigen source. From a group of 33 melanoma patients 14 reacted positively (42%) when fixed cultured cells were used, whereas, no positive reactions were found in a group of 14 control donors. However, a considerable proportion of patients with chronic inflammatory processes of the skin reacted positively (4/17 = 24%). A smaller proportion of positive reactions were found in melanoma patients when fixed melanoma cells from excised tumors were used (1/16 = 6%). The positive results in the group with chronic inflammatory processes may be explained as reactions against melanoma associated, but not melanoma-specific, antigens. Three possible reasons are discussed for the low frequency of positive reactions with cells from excised tumors: 1. the cells used in this study display only a few of the antigenic determinants typical for malignant melanoma, 2. antigen expression is quantitatively lower. 3. the surface antigens are covered by blocking factors.

Antigens, Neoplasm↗

Membrane associated antigens of human malignant melanoma. I. Internal labeling, detergent solubilization and characterization by homologous antisera and polyacrylamide gel electrophoresis.

Cultured melanoma cells were labeled with 3H-leucine over a period of 1-3 days. The labeled cells were mechanically disrupted and a preparation of "extranuclear membranes" was obtained by differential centrifugation. The membrane fragments were solubilized by the nonionic detergent NP-40 and the soluble material was double precipitated with antisera from melanoma patients and anti-human immunoglobulin sera. Because of the small quantitative differences of precipitated radiolabeled material between control and melanoma patients' sera, the precipitates were further analyzed on SDS-containing polyacrylamide gels. The labeled profiles of experimental and control gels now revealed clearcut differences usually seen in 2-3 characteristic peaks in the molecular weight range from 130,000-330,000.

Antigens, Neoplasm↗

Flow cytometric evaluation of the effects of doxorubicin on rat spermatogenesis.

Histopathologic examination of testicular tissue allows testicular impairment to be investigated. As an alternative to histopathology, flow cytometry (FCM) using a triple staining technique that combines DNA-ploidy with mitochondria stainability and vimentin immunostaining has also been utilized to evaluate testicular damage. In this article we evaluate the effects on spermatogenesis after acute exposure of rats to doxorubicin. Testicular cell suspensions of treated and control animals were analyzed by FCM. This allows several cell types to be identified and quantified, giving a control pattern. Deviations from this control pattern are considered as an indication of testicular damage. Doxorubicin produced a depletion of spermatogonia as early as 3 d after treatment. This effect could be followed through the temporal evolution of spermatogenesis. Comparable results were obtained by histopathology. The presented results show that FCM is a suitable and sensitive method for the detection of testicular damage. The advantages of FCM over other techniques include its rapidity and objectivity.

Animals↗

New and traditional approaches for the assessment of testicular toxicity.

In this study, the suitability of several methods for the assessment of testicular damage, including histopathology, flow cytometry (FCM), testicular sperm head counts, and secretion of androgen binding protein (ABP), has been evaluated. Testicular toxicity after acute exposure of adult rats to different doses of the known toxicant 1,3-dinitrobenzene (DNB) was analyzed. The effects showed dose dependence, in spite of the large variability within each dose group. Histopathology and FCM showed germ cell depletion, particularly of round spermatids; testicular sperm head counts were reduced and ABP production was increased. All evaluated methods showed similar sensitivities. The increased testicular ABP levels support the theory that the Sertoli cell is the likely target of DNB induced testicular toxicity, producing subsequent germ cell depletion. The presented results show the suitability of FCM for the analysis of testicular damage and also support the usefulness of including a metabolic marker for Sertoli cell function.

Androgen-Binding Protein↗

The usefulness of single and combined clinical characteristics for the diagnosis of dysplastic naevi.

A total of 761 melanocytic lesions were studied to elucidate the usefulness of clinical features for the diagnosis of dysplastic naevi. Characteristics associated with high (irregular border, irregular pigmentation), intermediate (black coloured areas, largest diameter greater than 0.5 cm, change of size, change of colour) and low diagnostic efficiency could be defined. Combinations of criteria had high sensitivities: at least one of the following four criteria was positive in 96% of the dysplastic naevi and in all melanomas with less pronounced clinical characteristics: irregular border, irregular pigmentation, greatest diameter greater than 0.5 cm, black coloured areas. A lesion is therefore unlikely to be a dysplastic naevus or a melanoma if all these criteria are absent. When change of size and change of colour were analysed in addition to the features mentioned above a sensitivity of 0.96 was found for at least two of these six criteria. At least three of these six criteria were observed in all melanomas with less pronounced clinical characteristics. However, a rather low specificity (0.19 for at least one of four positive criteria, 0.20 for at least two of six positive criteria) indicated that dysplastic and non-dysplastic naevi cannot be clinically differentiated with acceptable certainty. With less stringent histological criteria approximately twice as high specificities were found. Specificities were about twice as high in a subgroup of patients with at least one proven dysplastic naevus besides the lesion under diagnostic consideration. This facilitates the identification of individuals at risk of developing a melanoma.

Adolescent↗