Hypoxia-mediated apoptosis in oral carcinoma cells occurs <it>via </it>two independent pathways

<p>Abstract</p> <p>Background</p> <p>We are attempting to elucidate the mechanism of apoptotic cell death induced by hypoxia in oral cancer cells. Since hypoxia can render solid tumors more resistant to radiation and chemotherapy, understanding the pathways involved in...

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Main Authors: Zacharias Wolfgang, Vigneswaran Nadarajah, Nagaraj Nagathihalli S
Format: Article
Language:English
Published: BMC 2004-12-01
Series:Molecular Cancer
Online Access:http://www.molecular-cancer.com/content/3/1/38
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spelling doaj-36c1304d76df4171aaebf58b16dbc4ed2020-11-25T01:47:06ZengBMCMolecular Cancer1476-45982004-12-01313810.1186/1476-4598-3-38Hypoxia-mediated apoptosis in oral carcinoma cells occurs <it>via </it>two independent pathwaysZacharias WolfgangVigneswaran NadarajahNagaraj Nagathihalli S<p>Abstract</p> <p>Background</p> <p>We are attempting to elucidate the mechanism of apoptotic cell death induced by hypoxia in oral cancer cells. Since hypoxia can render solid tumors more resistant to radiation and chemotherapy, understanding the pathways involved in hypoxia-induced apoptosis of oral cancer cells would be of significant therapeutic value.</p> <p>Results</p> <p>Here we showed that oral cancer cells from primary tumor and lymph node metastasis undergo apoptosis after 24 to 48 h of hypoxia. During hypoxic growth, an increase in caspase-3 proteolytic activity was observed, accompanied by the cleavage of PARP (poly (ADP-ribose) polymerase) indicative of caspase activity. In addition, hypoxic stress also lead to activation of caspase-8, -9, and -10 but not -1, elicited the release of cytochrome C into the cytosol, and resulted in internucleosomal DNA fragmentation.</p> <p>Conclusion</p> <p>These results show that hypoxia-induced apoptosis in oral carcinoma cell lines relies on both intrinsic (mitochondrial) and extrinsic (cell death receptor mediated) pathways. This novel evidence will assist in designing more efficient combination chemotherapy approaches as promising strategy for the treatment of oral cancers.</p> http://www.molecular-cancer.com/content/3/1/38
collection DOAJ
language English
format Article
sources DOAJ
author Zacharias Wolfgang
Vigneswaran Nadarajah
Nagaraj Nagathihalli S
spellingShingle Zacharias Wolfgang
Vigneswaran Nadarajah
Nagaraj Nagathihalli S
Hypoxia-mediated apoptosis in oral carcinoma cells occurs <it>via </it>two independent pathways
Molecular Cancer
author_facet Zacharias Wolfgang
Vigneswaran Nadarajah
Nagaraj Nagathihalli S
author_sort Zacharias Wolfgang
title Hypoxia-mediated apoptosis in oral carcinoma cells occurs <it>via </it>two independent pathways
title_short Hypoxia-mediated apoptosis in oral carcinoma cells occurs <it>via </it>two independent pathways
title_full Hypoxia-mediated apoptosis in oral carcinoma cells occurs <it>via </it>two independent pathways
title_fullStr Hypoxia-mediated apoptosis in oral carcinoma cells occurs <it>via </it>two independent pathways
title_full_unstemmed Hypoxia-mediated apoptosis in oral carcinoma cells occurs <it>via </it>two independent pathways
title_sort hypoxia-mediated apoptosis in oral carcinoma cells occurs <it>via </it>two independent pathways
publisher BMC
series Molecular Cancer
issn 1476-4598
publishDate 2004-12-01
description <p>Abstract</p> <p>Background</p> <p>We are attempting to elucidate the mechanism of apoptotic cell death induced by hypoxia in oral cancer cells. Since hypoxia can render solid tumors more resistant to radiation and chemotherapy, understanding the pathways involved in hypoxia-induced apoptosis of oral cancer cells would be of significant therapeutic value.</p> <p>Results</p> <p>Here we showed that oral cancer cells from primary tumor and lymph node metastasis undergo apoptosis after 24 to 48 h of hypoxia. During hypoxic growth, an increase in caspase-3 proteolytic activity was observed, accompanied by the cleavage of PARP (poly (ADP-ribose) polymerase) indicative of caspase activity. In addition, hypoxic stress also lead to activation of caspase-8, -9, and -10 but not -1, elicited the release of cytochrome C into the cytosol, and resulted in internucleosomal DNA fragmentation.</p> <p>Conclusion</p> <p>These results show that hypoxia-induced apoptosis in oral carcinoma cell lines relies on both intrinsic (mitochondrial) and extrinsic (cell death receptor mediated) pathways. This novel evidence will assist in designing more efficient combination chemotherapy approaches as promising strategy for the treatment of oral cancers.</p>
url http://www.molecular-cancer.com/content/3/1/38
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AT vigneswarannadarajah hypoxiamediatedapoptosisinoralcarcinomacellsoccursitviaittwoindependentpathways
AT nagarajnagathihallis hypoxiamediatedapoptosisinoralcarcinomacellsoccursitviaittwoindependentpathways
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