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Eosinophil mediators & their toxicity on Breast Cancer cells

Eosinophil mediators & their toxicity on Breast Cancer cellsvon Michelle Law Sie sparen 16% des UVP sparen 16%
Über Eosinophil mediators & their toxicity on Breast Cancer cells

Eosinophils are known for their role as anti-helminthic agents & as inflammatory effectors in allergic hypersensitivity &bronchial asthma. Their granules contain extremely cytotoxic proteins which are responsible for damage to the normal epithelia, & contribute to allergic responses & the onset of asthma. Preliminary observations had shown tumor cell growth was inhibited by a crude eosinophil protein extract & partially inhibited by IL-4 & TNF-¿; also produced by eosinophils. Characterization of the protein isolated from the granules confirmed its identity as that of the eosinophil major basic protein as demonstrated by silver stain & western blot. The growth of both cancer cell lines was significantly inhibited by the protein isolate alone & in combination with select inflammatory & non-inflammatory cytokines. Additional results showed that the combination of protein isolate and selected cytokines differentially down-regulated the expression of oncogenes in the cell lines. The results demonstrate the functional potency of this eosinophil granular mediator in inhibiting in vitro tumor cell growth & suggest an effector role for this cell in the host response against breast cancer.

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  • Sprache:
  • Englisch
  • ISBN:
  • 9783659936524
  • Einband:
  • Taschenbuch
  • Seitenzahl:
  • 108
  • Veröffentlicht:
  • 25. August 2016
  • Abmessungen:
  • 150x7x220 mm.
  • Gewicht:
  • 179 g.
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Beschreibung von Eosinophil mediators & their toxicity on Breast Cancer cells

Eosinophils are known for their role as anti-helminthic agents & as inflammatory effectors in allergic hypersensitivity &bronchial asthma. Their granules contain extremely cytotoxic proteins which are responsible for damage to the normal epithelia, & contribute to allergic responses & the onset of asthma. Preliminary observations had shown tumor cell growth was inhibited by a crude eosinophil protein extract & partially inhibited by IL-4 & TNF-¿; also produced by eosinophils. Characterization of the protein isolated from the granules confirmed its identity as that of the eosinophil major basic protein as demonstrated by silver stain & western blot. The growth of both cancer cell lines was significantly inhibited by the protein isolate alone & in combination with select inflammatory & non-inflammatory cytokines. Additional results showed that the combination of protein isolate and selected cytokines differentially down-regulated the expression of oncogenes in the cell lines. The results demonstrate the functional potency of this eosinophil granular mediator in inhibiting in vitro tumor cell growth & suggest an effector role for this cell in the host response against breast cancer.

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