Evaluation of glycophenotype in breast cancer by quantum dot-lectin histochemistry
نویسندگان
چکیده
Cell surface glycoconjugates play an important role in differentiation/dedifferentiation processes and lectins are employed to evaluate them by several methodologies. Fluorescent probes are considered a valuable tool because of their ability to provide a particular view, and are more detailed and sensitive in terms of cell structure and molecular content. The aim of this study was to evaluate and compare the expression and distribution of glycoconjugates in normal human breast tissue, and benign (fibroadenoma), and malignantly transformed (invasive ductal carcinoma) breast tissues. For this, we used mercaptosuccinic acid-coated Cadmium Telluride (CdTe) quantum dots (QDs) conjugated with concanavalin A (Con A) or Ulex europaeus agglutinin I (UEA I) lectins to detect α-D-glucose/mannose and L-fucose residues, respectively. The QD-lectin conjugates were evaluated by hemagglutination activity tests and carbohydrate inhibition assays, and were found to remain functional, keeping their fluorescent properties and carbohydrate recognition ability. Fluorescence images showed that different regions of breast tissue expressed particular types of carbohydrates. While the stroma was preferentially and intensely stained by QD-Con A, ductal cells were preferentially labeled by QD-UEA I. These results indicate that QD-lectin conjugates can be used as molecular probes and can help to elucidate the glycoconjugate profile in biological processes.
منابع مشابه
مطالعه قند انتهایی گالاکتوزان استیل گالاکتوز آمین در گلیکوکونژوگه های سطحی سلول در فیبروآدنوما و کارسینوم اینترا داکتال پستان
Background and purpose : Despite the impressive progress in diagnosis and treatment of breast cancer, due to late diagnosis and metastasis to lymph nodes, it is still the leading cause of mortality in women. New studies showed a few changes in cell surface glycoconjugate in a few organs in process of neoplasia. The aim of the present study was to recognize Gal/GalNac in cell surface glycocon...
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