<?xml version="1.0" encoding="UTF-8"?>
<rss xmlns:dc="http://purl.org/dc/elements/1.1/" version="2.0">
  <channel>
    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/32772</link>
    <description />
    <pubDate>Wed, 15 Apr 2026 12:47:56 GMT</pubDate>
    <dc:date>2026-04-15T12:47:56Z</dc:date>
    <item>
      <title>The role of protein tyrosine kinases and phosphatases in cell signaling</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/77640</link>
      <description>Title: The role of protein tyrosine kinases and phosphatases in cell signaling
Abstract: Tyrosine phosphorylation is one of the earlier, highly organised events involved in the signal transduction&#xD;
cascade. This study was aimed at seeking more information concerning the role and site of action of the&#xD;
protein tyrosine kinases and phosphatases, and to identify any cross talk between their pathways and other&#xD;
systems. This was achieved with the use of pharmacological inhibitors applied in experiments, which&#xD;
measured physiological cell responsiveness.
Description: M.PHIL.</description>
      <pubDate>Fri, 01 Jan 1999 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/77640</guid>
      <dc:date>1999-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>The role of protein tyrosine kinases and phosphatases in cell signaling</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/32810</link>
      <description>Title: The role of protein tyrosine kinases and phosphatases in cell signaling
Abstract: Tyrosine phosphorylation is one of the earlier, highly organised events involved in the signal transduction&#xD;
cascade. This study was aimed at seeking more information concerning the role and site of action of the&#xD;
protein tyrosine kinases and phosphatases, and to identify any mm talk between their pathways and other&#xD;
systems. This was achieved with the use of pharmacological inhibitors applied in experiments, which&#xD;
measured physiological cell responsiveness.&#xD;
Various functional responses, namely activation of the N.IDPH oxidase system, arachidonic acid release&#xD;
and changes in intracellular calcium, which were stimulated by chemotactic peptide were assessed in the&#xD;
human neutrophil. Tyrosine kinases were found to have a significant role in the stimulation of the&#xD;
NADPH oxidase system. 7.4~f of the tyrosine kinase inhibitor genistein reduced superoxide anion&#xD;
generation to 20.0% (±7.6% S.E.M) of control V rna.&lt; values (p&lt;O.OS) and to 11.3% (±1.6% S.E.M) of&#xD;
control O.D.M. values (p&lt;0.01). It was additionally established that tyrosine kinases act in concert with&#xD;
PKC: in the generation of superoxicie anions. 5 IlM of genistein alone caused a 37.5% (±1.1 % S.E.M.)&#xD;
reduction in control V rn:u values. When used in combination with 30 ru\f of the PKC inhibitor&#xD;
staurosporine, which alone caused 2•+.0% (±5.12% S.E.M.) inhibition, a resulting 66.1% (1.5% ±S.E.M.)&#xD;
inhibition of superoxide formulation occurred. The effect of the tyrosine phosphatases on fi\fLP-induced&#xD;
neutrophil responses was found to be less significant than that of the tyrosine kinases, suggesting a more&#xD;
complex signalling mechanism, involving different subsets of phosphatases.&#xD;
The promycloid U937 cell line was used to overcome limiting factors when using human neutrophils.&#xD;
Since this cell line develops properties of host-defence cells when stimulated, it has been used as a&#xD;
simplified model for studying the properties of polymorphonuclear cells. In this study, the U937 cell line&#xD;
was used to examine a role for the phosphatases in the tyrosine phosphorylation of the Nck adapter&#xD;
oncoprotein. In this study, the presence of an endogenous anti-phosphatase was hypothesised, since&#xD;
tyrosine phosphorylation of Nck, which is present in both the stimulated and unstimulated form of U937&#xD;
cells, was reduced upon incubation with the tyrosine phosphatase inhibitor. This indicates that the antitumour&#xD;
effect of dephostatin may be mediated via the indirect inhibition of the tyrosine phosphorylation&#xD;
of this oncoprotein.
Description: M.PHIL.</description>
      <pubDate>Fri, 01 Jan 1999 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/32810</guid>
      <dc:date>1999-01-01T00:00:00Z</dc:date>
    </item>
  </channel>
</rss>

