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    <title>NISCAIR Online Periodicals Repository Collection: IJEB Vol.49(11) [November 2011]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12957</link>
    <description>&lt;b&gt;Special Issue on Emerging Trends in Cancer: Prevention and Therapeutics&lt;/b&gt;</description>
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    <title>The Collection's search engine</title>
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    <link>http://nopr.niscair.res.in/simple-search</link>
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/13006">
    <title>Transforming growth factor &lt;img src='/image/spc_char/beta.gif' border=0&gt; 2: A predictive marker for breast cancer</title>
    <link>http://nopr.niscair.res.in/handle/123456789/13006</link>
    <description>Title: Transforming growth factor &lt;img src='/image/spc_char/beta.gif' border=0&gt; 2: A predictive marker for breast cancer
&lt;br/&gt;
&lt;br/&gt;Authors: Dave, Heena; Trivedi, Sunil; Shah, Manoj; Shukla, Shilin
&lt;br/&gt;
&lt;br/&gt;Abstract: Dual role of TGF-&lt;img src='/image/spc_char/beta.gif' border=0&gt; signaling in breast tumorigenesis as an inhibitor in&#xD;
early stages and promoter in advanced stages has been well established and known&#xD;
as TGF-&lt;img src='/image/spc_char/beta.gif' border=0&gt; switch. However, the biological mechanisms needs to be explored. Aim&#xD;
of the present study was to look for the usefulness of TGF-&lt;img src='/image/spc_char/beta.gif' border=0&gt;2 as a predictive&#xD;
marker for breast cancer and to offer a better predictability to identify&#xD;
patients likely to benefit from antiTGF-&lt;img src='/image/spc_char/beta.gif' border=0&gt; strategies. Circulatory as well as&#xD;
transcript levels of TGF-&lt;img src='/image/spc_char/beta.gif' border=0&gt;2 were estimated from 118 pretherapeutic breast&#xD;
cancer patients using ELISA and q-PCR with ddCt method. Multifactorial analysis&#xD;
was performed to correlate the results to clinico-pathological prognosticators&#xD;
and Kaplan-Meier survival analysis with a median follow-up of 49 months was&#xD;
also evaluated. Circulating TGF-&lt;img src='/image/spc_char/beta.gif' border=0&gt;2 was similar in control and breast cancer patients. TGF-&lt;img src='/image/spc_char/beta.gif' border=0&gt;2 was&#xD;
significantly upregulated in advanced tumors compared to early tumors. An&#xD;
inverse correlation was observed between TGF-&lt;img src='/image/spc_char/beta.gif' border=0&gt;2 protein and mRNA; nevertheless both exhibited significant&#xD;
correlations with clinico-pathological prognosticators. Higher expression of TGF-&lt;img src='/image/spc_char/beta.gif' border=0&gt;2 mRNA was connected to an early relapse in advanced stage than early stage&#xD;
patients. It is the first report to evaluate circulatory and&#xD;
transcript levels exhibiting TGF-&lt;img src='/image/spc_char/beta.gif' border=0&gt; switch and confirming the utility of TGF-&lt;img src='/image/spc_char/beta.gif' border=0&gt;2 as an important&#xD;
predictive marker for breast cancer.
&lt;br/&gt;
&lt;br/&gt;Page(s): 879-887</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/13005">
    <title>Induction of apoptosis by eugenol in human breast cancer cells</title>
    <link>http://nopr.niscair.res.in/handle/123456789/13005</link>
    <description>Title: Induction of apoptosis by eugenol in human breast cancer cells
&lt;br/&gt;
&lt;br/&gt;Authors: Vidhya, N; Devaraj, S Niranjali
&lt;br/&gt;
&lt;br/&gt;Abstract: In the present study, potential anticancer effect of eugenol on inhibition&#xD;
of cell proliferation and induction of apoptosis in human MCF-7 breast cancer&#xD;
cells was investigated. Induction of cell death by eugenol was evaluated&#xD;
following MTT assay and monitoring lactate dehydrogenase released into the&#xD;
culture medium for cell viability and cytotoxicity, giemsa staining for&#xD;
morphological alterations, fluorescence microscopy analysis of cells using&#xD;
ethidium bromide and acridine orange and quantitation of DNA fragments for&#xD;
induction of apoptosis. Effect of eugenol on intracellular redox status of the&#xD;
human breast cancer cells was assessed by determining the level of glutathione&#xD;
and lipid peroxidation products (TBARS). Eugenol treatment inhibited the growth&#xD;
and proliferation of human MCF-7 breast cancer cells through induction of cell&#xD;
death, which was dose and time dependent. Microscopic examination of eugenol&#xD;
treated cells showed cell shrinkage, membrane blebbing and apoptotic body&#xD;
formation. Further, eugenol treatment also depleted the level of intracellular&#xD;
glutathione and increased the level of lipid peroxidation. The dose dependent&#xD;
increase in the percentage of apoptotic cells and DNA fragments suggested that&#xD;
apoptosis was involved in eugenol induced cell death and apoptosis might have&#xD;
played a role in the chemopreventive action of eugenol.
&lt;br/&gt;
&lt;br/&gt;Page(s): 871-878</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/13004">
    <title>Chemomodulatory potential of &lt;i style=""&gt;Glycine max &lt;/i&gt;against murine skin and cervical papillomagenesis</title>
    <link>http://nopr.niscair.res.in/handle/123456789/13004</link>
    <description>Title: Chemomodulatory potential of &lt;i style=""&gt;Glycine max &lt;/i&gt;against murine skin and cervical papillomagenesis
&lt;br/&gt;
&lt;br/&gt;Authors: Singh, M; Mendez, E; Rao, A Ramesha; Kale, R K
&lt;br/&gt;
&lt;br/&gt;Abstract: In&#xD;
the present study, chemopreventive potential of &lt;i style=""&gt;Glycine max (G. Max) &lt;/i&gt;seeds was examined against DMBA-induced skin&#xD;
and MCA-induced cervical papillomagenesis in Swiss albino mice. Different doses&#xD;
(2.5, 5, and 7.5% w/w) of &lt;i style=""&gt;G. max&lt;/i&gt; were&#xD;
provided to animals in feed. Results exhibited a significant reduction in skin&#xD;
as well as cervical tumor incidence and tumor multiplicity (up to 75%) at all&#xD;
doses of test diet as compared to the control. Relatively, 7.5% test diet was&#xD;
most effective in protecting the animals against carcinogenesis. Further, detoxifying&#xD;
enzymes and antioxidative status was also evaluated in the liver of mice to&#xD;
understand the role of &lt;i style=""&gt;G. max&lt;/i&gt; in&#xD;
prevention of cancer. It was observed that the test diet containing &lt;i style=""&gt;G. max&lt;/i&gt; significantly elevated the&#xD;
specific activities of glutathione-S-transferase (GST), DT-diaphorase (DTD),&#xD;
superoxide dismutase (SOD), catalase (CAT), and glyoxalase I (Gly I). The test&#xD;
diet also elevated the content of reduced glutathione whereas it decreased the&#xD;
level of the peroxidative damage along with the specific activity of lactate&#xD;
dehydrogenase. It appeared that &lt;i style=""&gt;G. max&lt;/i&gt;&#xD;
seeds provided chemoprevention against skin and cervical papillomagenesis&#xD;
probably by modulating the detoxifying and antioxidative enzymes. It could be&#xD;
inferred that intake of &lt;i style=""&gt;G. max&lt;/i&gt; might&#xD;
help in reducing the risk of cancer.
&lt;br/&gt;
&lt;br/&gt;Page(s): 864-870</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/13003">
    <title>Chemoprotective influence of &lt;i style=""&gt;Zanthoxylum&lt;/i&gt; sps. on hepatic carcinogen metabolizing and antioxidant enzymes and skin papillomagenesis in murine model</title>
    <link>http://nopr.niscair.res.in/handle/123456789/13003</link>
    <description>Title: Chemoprotective influence of &lt;i style=""&gt;Zanthoxylum&lt;/i&gt; sps. on hepatic carcinogen metabolizing and antioxidant enzymes and skin papillomagenesis in murine model
&lt;br/&gt;
&lt;br/&gt;Authors: Rajamani, Paulraj; Banerjee, Sanjeev; Rao, A Ramesha
&lt;br/&gt;
&lt;br/&gt;Abstract: In the present study, the putative potential of pericarp of dried&#xD;
fruit of &lt;i style=""&gt;Zanthoxylum&lt;/i&gt; (Rutaceae&#xD;
Family), a common spice additive in India’s west coast cuisines, in&#xD;
protecting against carcinogenesis has been reported. Extract from dried fruit&#xD;
of &lt;i style=""&gt;Zanthoxylum&lt;/i&gt; was orally administered&#xD;
to mice at two dose levels: 100 and 200 mg/kg body wt. for 14 days. Results&#xD;
reveal bifunctional nature of &lt;i style=""&gt;Zanthoxylum&lt;/i&gt;&#xD;
species as deduced from its potential to induce phase-I and phase-II enzyme&#xD;
activities associated with carcinogen activation and detoxification in the&#xD;
liver of mice. Hepatic glutathione S-transferase and &#xD;
DT-diaphorase were found significantly elevated by the treatment. &lt;i style=""&gt;Zanthoxylum&lt;/i&gt; was also effective in&#xD;
augmenting the antioxidant enzyme activities of glutathione peroxidase,&#xD;
superoxide dismutase and catalase albeit significantly by high dose of the&#xD;
extract (&lt;i style=""&gt;P&lt;/i&gt;&lt;0.05; &lt;i style=""&gt;P&lt;/i&gt;&lt;0.01). Reduced glutathione was also&#xD;
significantly elevated in the liver of treated animals (&lt;i style=""&gt;P&lt;/i&gt;&lt;0.05). The present study also investigated peri-initiation&#xD;
application of acetone extract of &lt;i style=""&gt;Zanthoxylum&lt;/i&gt;&#xD;
on initiated mouse skin. Results showed a significant reduction in tumor&#xD;
incidence from 68% to 36% (&lt;i style=""&gt;P&lt;/i&gt;&lt;0.05);&#xD;
as well as, a reduction in tumor burden per effective mouse from 3.87 to 0.72 (&lt;i style=""&gt;P&lt;/i&gt;&lt;0.01). Cumulatively, the findings&#xD;
strongly suggest cancer chemo-preventive potential of &lt;i style=""&gt;Zanthoxylum&lt;/i&gt; sps.
&lt;br/&gt;
&lt;br/&gt;Page(s): 857-863</description>
  </item>
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